BACKGROUND OF THE INVENTION It is well-known that 1α,25-Dihydroxyvitamin D3 has various physiological activities and is widely used as various pharmaceuticals. For example, the pharmaceutical agent containing 1α,25-Dihydroxyvitamin D3 as active ingredient marketed as ROCALTROL (™) and used for the treatment of psoriasis and secondary hyperparathyroidism. However, it is also well-known that 1α,25-Dihydroxyvitamin D3 has a serious side effect elevating serum calcium level and sometimes it leads to hypercalcemia. Because of this side effect, there are some limitations in administering 1α,25-Dihydroxyvitamin D3, such as, for example, limitation of maximum administration dosages or limitation of patients to be treated, and therefore, the benefit of the various physiological activities of the compound for treating diseases cannot be fully redlined. To overcome this problem, various derivatives of vitamin D3 have been synthesized, and recently, mimic compounds of the vitamin D3 not having a secosteroidal structure (VD3 mimics) were suggested. For example, International Publication No. WO00/10958 and corresponding U.S. Patent 6,218,430 B1 disclose bisphenyl compounds useful as VD3 mimics, however, no compound has been launched or tested in clinical trials. Accordingly, there is a demand for a vitamin D3 derivative with stronger physiological activities and weaker calcemic effect than VD3 mimics and compounds previously described.

SUMMARY OF THE INVENTION The present invention relates to bisphenyl compounds useful as modulators of the vitamin D receptor activity or their synthetic intermediates, represented by formula I:

R4 R6 i wherein X is an optionally substituted methylene, an optionally substituted ethylene, an optionally substituted vinylene, an ethynylene, -S(O)n-, -NH-, or -O-; n is an integer of 0 to 2; Y is COOR8, CON(R9)R10, S(0)mR11 or a substituent represented by following formula: OR (CH2)a \^Ri2 R-13 R8 and R11 are each independently selected from an optionally substituted C1-10 alkyl group or an optionally substituted C3-10 cycloalkyl group; R9 and R10 are each independently selected from a hydrogen atom, an optionally substituted C1-10 alkyl group or an optionally substituted C3-10 cycloalkyl group; m is an integer of 0 to 2; a is an integer of 0 to 3; R is a hydrogen atom or a protecting group for a hydroxyl group; R12 and R13 are each independently selected from the group consisting of a hydrogen atom, an optionally substituted C1-10 alkyl group, an optionally substituted C3-10 cycloalkyl group, an optionally substituted C2-10 alkenyl group, an optionally substituted C2-10 alkynyl group, or R12 and R13 may together form an optionally substituted C3-C12 cycloalkyl group or an optionally substituted 3-12 membered heterocyclic group; W is a hydroxyl group, a carboxyl group, a trifluoromethanesulfonyloxy group or a substituent represented by following formula:

-Q-(CH2)b— ^R15 R-16 Q is -O-, -S-, -NH-, an optionally substituted methylene, an optionally substituted ethylene, an optionally substituted vinylene, an ethynylen, - (CH2)k-NHC(=O)-, -(CH2)k-C(=O)NH-, -(CH2)k-NHC(=O)NH-, -O-(CH2)k- NHC(=O)-, -O-(CH2)k-C(=O)NH-, -O-(CH2)k-NHC(=O)NH- or -(CH2)k-SO2-; b is an integer of 0 to 10; k is an integer of 0 to 2; R14 is a hydrogen atom, a hydroxyl group, an optionally substituted carboxyl group, an optionally substituted carbamoyl group, an optionally substituted C1-6 alkyl group, an optionally substituted C3-C12 cycloalkyl group, an optionally substituted C1-6 alkenyl group, an optionally substituted C1-6 alkynyl group, an optionally substituted C6-C12 aryl group, an optionally substituted (C6-C12)aryl-(C1-4)alkyl group, -OR17 or -N(R18)R19; R15 and R16 are each independently selected from the group consisting of a hydrogen atom, an optionally substituted C1-6 alkyl group, an optionally substituted C3-C12 cycloalkyl group, an optionally substituted C6- C12 aryl group, an optionally substituted (C6-C12)aryl-(C1-4)alkyl group, an optionally substituted 3-12 membered heterocyclic group, or R15 and R16 may together form =O; R17 is selected from an optionally substituted C1-6 alkyl group or an optionally substituted C3-C6 cycloalkyl group; R18 and R19 are each independently selected from the group consisting of a hydrogen atom, an optionally substituted C1-6 alkyl group, an optionally substituted C3-C6 cycloalkyl group, or R18 and R19 may together form an optionally substituted C3-C12 cycloalkyl group or an optionally substituted 3-12 membered heterocyclic group; or one of (R15 and R17), (R16 and R17), (R15 and R18), (R16 and R18), (R15 and R19) or (R16 and R19) may together form a 3-12 membered cyclic ring which is selected from the group consisting of an amidine ring, an amine ring, an ether ring, a lactam ring, a lactone ring, an acetal ring, a hemiacetal ring, a carbonate ring, a carbamate ring, an urea ring, combinations thereof; R1 and R2 are each independently selected from the group consisting of a C1-6 alkyl group optionally substituted with a halogen atom(s), a C3-6 cycloalkyl group optionally substituted with a halogen atom(s), a C2-6 alkenyl group optionally substituted with a halogen atom(s), a C2-6 alkynyl group optionally substituted with a halogen atom(s), or R1 and R2 may together form a C3-8 cycloalkyl group optionally substituted with a halogen atom(s), a C3-8 cycloalkenyl group optionally substituted with a halogen atom(s) or a C3-8 cycloalkylidene group optionally substituted with a halogen atom(s); R3, R4, R5 and R6 are each independently selected from the group consisting of a hydrogen atom, a halogen atom, a C1-6 alkyl group optionally substituted with a halogen atom(s), a C3-6 cycloalkyl group optionally substituted with a halogen atom(s); When X is -S(O)n-, -NH- or -O-, Q is selected from the group consisting of a methylene which may be substituted an C1-4 alkyl group, an ethylene, a vinylene, an ethynylene, -(CH2)k-NHC(=O)-, -(CH2)k-C(=O)NH-, - (CH2)k-NHC(=O)NH-, -(CH2)k-SO2-; When Q is -O-, -S-, -NH-, -O-(CH2)k-NHC(=O)-, -O-(CH2)k-C(=O)NH- or -O-(CH2)k-NHC(=O)NH-, X is selected from the group consisting of an optionally substituted methylene, an optionally substituted ethylene, an optionally substituted vinylene, an ethynylene; and pharmaceutically acceptable salts and prodrugs thereof. DETAILED DESCRIPTION OF THE INVENTION Definitions

"Optionally substituted" or "which may be substituted" means that the compounds of the present invention can optionally have one or more substituent(s) in that position. In the case having two or more substituents, each substituents can be same or different. A "halogen atom" according to the invention is a fluorine atom, a chlorine atom, a bromine atom or an iodine atom. A "C1-10 alkyl group" according to the invention is a linear or branched alkyl group of 1 to 10 carbons, such as a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec-butyl group, a tert-butyl group, a pentyl group, an isopentyl group, a neopentyl group, a tert-pentyl group, a hexyl group, an isohexyl group, a heptyl group, an octyl group, a nonyl group, a decyl group or the like. A "C1-6 alkyl group" according to the invention is a linear or branched alkyl group of 1 to 6 carbons, such as a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec- butyl group, a tert-butyl group, a pentyl group, an isopentyl group, a neopentyl group, a tert-pentyl group, a hexyl group, an isohexyl group or the like. A "C1-4 alkyl group" according to the invention is a linear or branched alkyl group of 1 to 3 carbons, such as a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, an isobutyl group, a sec- butyl group, a tert-butyl group or the like. A "C1-3 alkyl group" according to the invention is a linear or branched alkyl group of 1 to 3 carbons, such as a methyl group, an ethyl group, a propyl group, an isopropyl group or the like. A "C3-12 cycloalkyl group" according to the invention is a cyclic saturated hydrocarbon group of 3 to 12 carbons, such as a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, a cyclononyl group, a cyclodecyl group, a cycloundecyl group, a cyclododecyl group or the like. A "C3-10 cycloalkyl group" according to the invention is a cyclic saturated hydrocarbon group of 3 to 10 carbons, such as a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, a cyclononyl group, a cyclodecyl group or the like. A "C3-8 cycloalkyl group" according to the invention is a cyclic saturated hydrocarbon group of 3 to 8 carbons, such as a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group or the like. A "C3-6 cycloalkyl group" according to the invention is a cyclic saturated hydrocarbon group of 3 to 6 carbons, such as a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group or the like. A "C2-10 alkenyl group" according to the invention is a linear, branched or cyclic alkenyl group of 2 to 10 carbons, such as a vinyl group, an allyl group, an isopropenyl group, a 2-butenyl group, a 3-butenyl group, a 2-pentenyl group, a 3-pentenyl group, a 4-pentenyl group, a 1-cyclopentenyl group, a 2-hexenyl group, a 3-hexenyl group, a 4-hexenyl group, a 5-hexenyl group, a 1 -cyclohexenyl group or the like. A "C2-6 alkenyl group" according to the invention is a linear, branched or cyclic alkenyl group of 2 to 6 carbons, such as a vinyl group, an allyl group, an isopropenyl group, a 2-butenyl group, a 3-butenyl group, a 2- pentenyl group, a 3-pentenyl group, a 4-pentenyl group, a 1 -cyclopentenyl group, a 2-hexenyl group, a 3-hexenyl group, a 4-hexenyl group, a 5-hexenyl group, a 1 -cyclohexenyl group or the like. A "C3-8 cycloalkenyl group" according to the invention is a cyclic alkenyl group of 3 to 8 carbons, such as a 1 -cyclopentenyl group, a 1- cyclohexenyl group, 2-cyclohexenyl group or the like. A "C2-10 alkynyl group" according to the invention is a linear or branched alkynyl group of 2 to 10 carbons, such as an ethynyl group, a 2- propynyl group, a 2-butynyl group, a 3-butynyl group, a 2-pentynyl group, a 3-pentynyl group, a 4-pentynyl group, a 2-hexynyl group, a 3-hexynyl group, a 4-hexynyl group, a 5-hexynyl group or the like. A "C2-6 alkynyl group" according to the invention is a linear or branched alkynyl group of 2 to 6 carbons, such as an ethynyl group, a 2- propynyl group, a 2-butynyl group, a 3-butynyl group, a 2-pentynyl group, a 3-pentynyl group, a 4-pentynyl group, a 2-hexynyl group, a 3-hexynyl group, a 4-hexynyl group, a 5-hexynyl group or the like. A "C6-12 aryl group" according to the invention is an aryl group of 6 to 12 carbons, such as a phenyl group, a naphthyl group or the like. A "(C6-12)aryl-(C1-4)alkyl group" according to the invention is an alkyl group of 1 to 4 carbons with an aryl group of 6 to 12 carbons, such as a benzyl group, a phenethyl group, a 3-phenyl-propyl group, a 4-phenyl-butyl group, a naphthalen-1-yl-methyl group, a naphthalen-2-yl-methyl group or the like. A "3-12 membered heterocyclic group" according to the invention is a mono- and polycyclic group having 3 to 12 membered ring(s) wherein the ring(s) contains at least one heteroatom. Suitable heteroatoms include oxygen, nitrogen, sulfur, phosphorus and boron. Heterocyclic group may be attached at a carbon atom or heteroatom. Heterocyclic groups include an aziridine group, an azetidine group, an oxetane group, a pyrrolidine group, a tetrahydrofuran group, a pyrrole group, a furan group, a thiophene group, a pyrazole group, an isoxazole group, an isothiazole group, an imidazole group, an oxazole group, a thiazolegroup, a 1 ,2,5-oxadiazole group, a 1 ,3,4- oxadiazole group, a 1 ,3,4-thiadiazole group, a 1 ,2,4-oxadiazole group, a 1 ,2,4-thiadiazole group, a tetrazole group, a piperidine group, a pyridine group, a pyridazine group, a pyrimidine group, a pyrazine group, a tetrahydropyran group, a pyran group, a thiopyran group, an indole group, a benzofuran group, a benzothiophene group, an indazole group, a benzisoxazole group, a benzisothiazole group, a benzimidazole group, a benzoxazole group, a benzothiazole gorup, a quinoline group, an isoquinoline group, a cinnoline group, a phthalazine group, a quinazoline group, a quinoxaline group or the like. A "C1-8 alkoxy group" according to the invention is an oxygen group which is substituted with a linear or branched alkyl group, alkenyl group, alkynyl group, aralkyl group or aryl group of 1 to 8 carbons, such as a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group, a butoxy group, an isobutoxy group, a sec-butoxy group, a tert-butoxy group, a pentyloxy group, an isopentyloxy group, a hexyloxy group, an allyloxy, group, a 2-propynyloxy group, a benzyloxy group, a phenoxy group or the like. A "C3-8 cycloalkylidene group" according to the invention is a divalent group formed from cycloalkanes of 3 to 8 carbons by removal of two hydrogen atoms from the same carbon atom, the free valencies of which are part of a double bond. Examples of C3-8 cycloalkylidene groups are such as a cyclopentylidene group, a cyclohexylidene group, a cycloheptylidene group or the like. A"protecting group for a hydroxyl group" according to the invention is a substituent which is useful for protecting a hydroxyl group, such as a methoxymethyl group, a methylthiomethyl group, a (phenyldimethylsilyl)methoxymethyl group, a benzyloxymethyl group, a p- methoxybenzyloxymethyl group, a p-nitrobenzyloxymethyl group, an o- nitrobenzyloxymethyl group, a (4-methoxyphenoxy)methyl group, a guaiacol methyl group, a t-butoxymethyl group, a 4-pentenyloxymethyl group, a siloxymethyl group, a 2-methoxyethoxymethyl group, 2,2,2- trichloroethoxymethyl group, a bis(2-chloroethoxy)methyl group, a 2- (trimethylsilyl)ethoxymethyl group, a menthoxymethyl group, a tetrahydropyranyl group, a 3-bromotetrahydropyranyl group, a tertahydrothiopyranyl group, a 1 -methoxycyclohexyl group, 4- methoxytetrahydrothiopyranyl, a tetrahydrofuranyl group, a tetrahydrothiofuranyl group, a 1 -ethoxyethyl group, a 1-(2-chloroethoxy)ethyl group, a 1-[2-(trimethylsilyl)ethoxy]ethyl group, a 1-methyl-1-methoxyethyl group, a 1-methyl-1-benzyloxyethyl group, a 1-methyl-1-benzyloxy-2- fluoroethyl group, a 1-methyl- 1 -phenoxyethyl group, a 2,2,2-trichloroethyl group, a 1 ,1-dianisyl-2,2,2-trichloroethyl group, a 2-trimethylsilylethyl group, a 2-(benzylthio)ethyl group, a 2-(phenylselenyl)ethyl group, a t-butyl group, an allyl group, a propargyl group, a p-chlorophenyl group, a p- methoxyphenyl group, a p-nitrophenyl group, a 2,4-dinitrophenyl group, a benzyl group, a p-methoxybenzyl group, a 3, 4-dimethoxy benzyl group, an o- nitrophenyl group, a p-nitrophenyl group, a p-halobenzyl group, a 2,6- dichlorobenzyl group, a p-cyanobenzyl group, a p-phenyl benzyl group, a 2,6- difluorobenzyl group, a p-acylaminobenzyl group, a 2-triflluoromethyl benzyl group, a 2-picolyl group, a 4-picolyl group, a 2-quinolinylmethyl group, a triphenylmethyl group, a trimethylsilyl group, a triethylsilyl group, a triisopropylsilyl group, a dimethylisopropylsilyl group, a diethylisopropylsilyl group, a t-butyldimethylsilyl group, a t-buthyldiphenylsilyl group, a tribenzylsilyl group, a triphenylsilyl group, a diphenylmethylsilyl group, a di-t- buthylmethylsilyl group, tris(trimethylsilyl)silyl group, a formyl group, a benzoylformyl group, an acetyl group, a chloroacetyl group, a dichloroacetyl group, a trichloroacetyl group, a methoxyacetyl group, a pivaloyl group, a benzoyl group, a 2,4,6-trimethylbenzoyl group, a methylcarbonyloxy group, a methoxymethylcarbonyloxy group, an ethylcarbonyloxy group, an isobutylcarbonyloxy group, a vinylcarbonyloxy group, an allylcarbonyloxy group, a benzylcarbonyloxy group, a p-methoxybenzylcarbonyloxy group, an allylsulfonyl group, a methanesulfonyl group, a benzylsulfonyl group, a tosyl group, a trifluoromethanesulfonyl group or the like. The term "pharmaceutically acceptable prodrug" or "prodrug," as used herein, represents those prodrugs of the compounds of the present invention which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of humans and lower animals without undue toxicity, irritation, allergic response, and the like, commensurate with a reasonable benefit/risk ratio, and effective for their intended use. Prodrugs of the present invention may be rapidly transformed in vivo to a parent compound of formula (I), for example, by hydrolysis in blood. A through discussion is provided in T. Higuchi and V. Stella, Pro-drugs as Novel Delivery Systems, V. 14 of the A.C.S. Symposium Series, and in Edward B. Roche, ed., Bioreversible Carriers in drug Design, American Pharmaceutical Association and Pergamon Press (1987), hereby incorporated by reference.

The present invention offers bisphenyl compounds of formula I.

R1-/R2 ,R5

R4 Re I In the above fomula I, X is an optionally substituted methylene, an optionally substituted ethylene, an optionally substituted vinylene, an ethynylene, -S(O)n-, -NH-, or -O-. Preferable X is an optionally substituted methylene, an optionally substituted ethylene, an optionally substituted vinylene or an ethynylene. More preferable X is a methylene, an ethylene, a vinylene or an ethynylene a methylene. Furthermore preferable X is an ethylene, a vinylene or an ethynylene a methylene. "An optionally substituted methylene" is, in particular, a methylene which may be substituted with a halogen atom(s) and/or a C1-4 alkyl group(s), and is preferablely a methylene. "An optionally substituted vinylene" is, in particular, a vinylene which may be substituted with a halogen atom(s) and/or a C1-4 alkyl group(s), and is preferablely a vinylene. "An optionally substituted ethylene" is, in particular, an ethylene which may be substituted with a halogen atom(s) and/or a C1-4 alkyl group(s), and is preferablely an ethylene. In "-S(O)n-", n is an integer of 0 to 2, therefore, "-S(O)n-" means -S-, - SO- or -SO2-. In the above fomula I, Y is COOR8, CON(R9)R10, S(0)mR11 or a substituent represented by following formula: OR (CH2)a \~R-I2 Ri3 Preferable Y is a substituent represented by following formula: /OR — (CH2)a— f-Ri2 R-I3 In "COOR8", R8 is selected an optionally substituted C1-10 alkyl group or an optionally substituted C3-10 cycloalkyl group. In this case, "an optionally substituted C1-10 alkyl group" is, in particular, a C1-10 alkyl group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s), and is preferablely a C1-10 alkyl group. "An optionally substituted C3-10 cycloalkyl group" is, in particular, a C3-10 cycloalkyl group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s), and is preferablely a C3-10 cycloalkyl group. In "CON(R9)R10", R9 and R10 are each independently selected from a hydrogen atom, an optionally substituted C1-10 alkyl group or an optionally substituted C3-10 cycloalkyl group. In this case, "an optionally substituted C1-10 alkyl group" is, in particular, a C1-10 alkyl group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s), and is preferablely a C1- 10 alkyl group. "An optionally substituted C3-10 cycloalkyl group" is, in particular, a C3-10 cycloalkyl group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s), and is preferablely a C3-10 cycloalkyl group. In "S(O)mR11", m is an integer of 0 to 2, therefore, "S(O)mR11" means -S-R11 , -SO-R11 or -SO2-R11 , and R11 is selected an optionally substituted C1-10 alkyl group or an optionally substituted C3-10 cycloalkyl group. In this case, "an optionally substituted C1-10 alkyl group" is, in particular, a C1-10 alkyl group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s), and is preferablely a C1-10 alkyl group. "An optionally substituted C3-10 cycloalkyl group" is, in particular, a C3-10 cycloalkyl group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s), and is preferablely a C3-10 cycloalkyl group. When Y is a substituent represented by following formula: OR (CH2)a v Ri2 Ri3 , a is an integer of 0 to 3, and is preferablely 0. R is a hydrogen atom or a protecting group for a hydroxyl group. As a modulator of the vitamin D receptor activity, R is preferablely a hydrogen atom. The compound wherein R is a protecting group for a hydroxyl group is useful as a synthetic intermediate of a modulator of the vitamin D receptor activity. However, some of these compounds exhibit the vitamin D receptor modulating activity, and such compounds are also useful as a modulator of the vitamin D receptor activity. "A protecting group for a hydroxyl group" is, in particular, a methoxymethyl group, a methylthiomethyl group, a (phenyldimethylsilyl)methoxymethyl group, a benzyloxymethyl group, a p- methoxybenzyloxymethyl group, a p-nitrobenzyloxymethyl group, an o- nitrobenzyloxymethyl group, a (4-methoxyphenoxy)methyl group, a guaiacolmethyl group, a t-butoxymethyl group, a 4-pentenyloxymethyl group, a siloxymethyl group, a 2-methoxyethoxymethyl group, 2,2,2- trichloroethoxymethyl group, a bis(2-chloroethoxy)methyl group, a 2- (trimethylsilyl)ethoxymethyl group, a menthoxymethyl group, a tetrahydropyranyl group, a 3-bromotetrahydropyranyl group, a tertahydrothiopyranyl group, a 1-methoxycyclohexyl group, A- methoxytetrahydrothiopyranyl, a tetrahydrofuranyl group, a tetrahydrothiofuranyl group, a 1-ethoxyethyl group, a 1-(2-chloroethoxy)ethyl group, a 1-[2-(trimethylsilyl)ethoxy]ethyl group, a 1-methyl-1-methoxyethyl group, a 1-methyl- 1 -benzyloxyethy I group, a 1-methyl-1-benzyloxy-2- fluoroethyl group, a 1-methyl-1-phenoxyethyl group, a 2,2,2-trichloroethyl group, a 1 ,1-dianisyl-2,2,2-trichloroethyl group, a 2-tri methylsi IyI ethyl group, a 2-(benzylthio)ethyl group, a 2-(phenylselenyl)ethyl group, a t-butyl group, an allyl group, a propargyl group, a p-chlorophenyl group, a p- methoxyphenyl group, a p-nitrophenyl group, a 2,4-dinitrophenyl group, a benzyl group, a p-methoxybenzyl group, a 3,4-dimethoxybenzyl group, an o- nitrophenyl group, a p-nitrophenyl group, a p-halobenzyl group, a 2,6- dichlorobenzyl group, a p-cyanobenzyl group, a p-phenyl benzyl group, a 2,6- difluorobenzyl group, a p-acylaminobenzyl group, a 2-triflluoromethyl benzyl group, a 2-picolyl group, a 4-picolyl group, a 2-quinolinylmethyl group, a triphenylmethyl group, a trimethylsilyl group, a triethylsilyl group, a triisopropylsilyl group, a dimethylisopropylsilyl group, a diethylisopropylsilyl group, a t-butyldimethylsilyl group, a t-buthyldiphenylsilyl group, a tribenzylsilyl group, a triphenylsilyl group, a diphenylmethylsilyl group, a di-t- buthylmethylsilyl group, tris(trimethylsilyl)silyl group, a formyl group, a benzoylformyl group, an acetyl group, a chloroacetyl group, a dichloroacetyl group, a trichloroacetyl group, a methoxyacetyl group, a pivaloyl group, a benzoyl group, a 2,4,6-trimethylbenzoyl group, a methylcarbonyloxy group, a methoxymethylcarbonyloxy group, an ethylcarbonyloxy group, an isobutylcarbonyloxy group, a vinylcarbonyloxy group, an allylcarbonyloxy group, a benzylcarbonyloxy group, a p-methoxybenzylcarbonyloxy group, an allylsulfonyl group, a methanesulfonyl group, a benzylsulfonyl group, a tosyl group, a trifluoromethanesulfonyl group or the like. "A protecting group for a hydroxyl group" is preferablely selected from a methoxymethyl group, a 2- (trimethylsilyl)ethoxymethyl group, a tetrahydropyranyl group, a benzyl group, a p-methoxybenzyl group, a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a t-buthyldiphenylsilyl group, an acetyl group, a pivaloyl group, a benzoyl group, a methanesulfonyl group, a tosyl group or a trifluoromethanesulfonyl group. R12 and R13 are each independently selected from the group consisting of a hydrogen atom, an optionally substituted C1-10 alkyl group, an optionally substituted C3-10 cycloalkyl group, an optionally substituted C2-10 alkenyl group, an optionally substituted C2-10 alkynyl group, or R12 and R13 may together form an optionally substituted C3-C12 cycloalkyl group or an optionally substituted 3-12 membered heterocyclic group. R12 and R13 are preferablely each independently selected from the group consisting of a hydrogen atom, an optionally substituted C1-10 alkyl group, an optionally substituted C3-10 cycloalkyl group, an optionally substituted C2-10 alkenyl group, an optionally substituted C2-10 alkynyl group, or R12 and R13 may together form an optionally substituted C3-C12 cycloalkyl group. R12 and R13 are more preferablely each independently selected from the group consisting of a hydrogen atom, a C1-8 alkyl group which may be substituted with a halogen atom(s), a C3-8 cycloalkyl group which may be substituted with a C1-4 alkyl group, or R12 and R13 are together form a C3- 8 cycloalkyl group which may be substituted with a C1-4 alkyl group. R12 and R13 are furthermore preferablely each independently selected from the group consisting of a hydrogen atom, a C1-6 alkyl group which may be substituted with a halogen atom(s), a C3-8 cycloalkyl group which may be substituted with a C1-4 alkyl group, or R12 and R13 are together form a C3- 8 cycloalkyl group. Especially, R12 and R13 are preferablely selected from the group consisting of i) one of R12 and R13 is a hydrogen atom and the other is a C1-6 alkyl group, ii) one of R12 and R13 is a hydrogen atom and the other is a C3-8 cycloalkyl group which may be substituted with a C1-4 alkyl group, iii) both of R12 and R13 are same and a C1-6 alkyl group which may be substituted with a halogen atom(s), or R12 and R13 are together form a C3-10 cycloalkyl group. One of the preferred combinations of R12 and R13 are, in particular, a hydrogen atom and a tert-butyl group, or both a trifluoromethyl group. In this case, "an optionally substituted C1-10 alkyl group" is, in particular, a C1-10 alkyl group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s), and is preferablely a C1-10 alkyl group. "An optionally substituted C1-10 alkenyl group" is, in particular, a C1-10 alkenyl group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s), and is preferablely a C1-10 alkenyl group. "An optionally substituted C1-10 alkynyl group" is, in particular, a C1-10 alkynyl group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s), and is preferablely a C1-10 alkynyl group. "An optionally substituted C3-10 cycloalkyl group" is, in particular, a C3-10 cycloalkyl group which may be substituted with a halogen atom(s), a hydroxy! group(s), an amino group(s), a carboxyl group(s), a C1-4 alkyl group and/or a C1-8 alkoxy group(s), and is preferablely a C3-10 cycloalkyl group which may be substituted with a C1-4 alkyl group. "An optionally substituted 3-12 membered heterocyclic group" is, in particular, a 3-12 membered heterocyclic group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s). In the above fomula I, W is a hydroxyl group, a carboxyl group, a trifluoromethanesulfonyloxy group or a substituent represented by following formula:

— Q-(CH2)b— f-R15 Ri6 As a modulator of the vitamin D receptor activity, W is preferablely a substituent represented by following formula: yR-14 Q— (CH2)b \~Ri5 R-I6 Among them, especially as pharmaceuticals for the treatment of osteoporosis, the compound having a carboxyl group at its terminal end is preffered. On the other hand, the compound wherein W is a hydroxyl group, a carboxyl group or a trifluoromethanesulfonyloxy group is useful as a synthetic intermediate of a modulator of the vitamin D receptor activity. However, some of these compounds exhibit the vitamin D receptor modulating activity, and such compounds are also useful as a modulator of the vitamin D receptor activity. When Y is a substituent represented by following formula: /Ri4 Q— (CH2)b ^~R-i5 Ri6 , b is an integer of 0 to 10, is preferablely an integer of 0 to 5, and is more preferablely 0, 1 or 2. Q is -O-, -S-, -NH-, an optionally substituted methylene, an optionally substituted ethylene, an optionally substituted vinylene, an ethynylene, - (CH2)k-NHC(=O)-, -(CH2)k-C(=O)NH-, -(CH2)k-NHC(=O)NH-, -O-(CH2)k- NHC(=O)-, -O-(CH2)k-C(=O)NH-, -O-(CH2)k-NHC(=O)NH- or -(CH2)k-SO2-. Preferable Q is selected from -O-, a methylene, an ethylene, a vinylene, an ethynylene, -(CH2)k-C(=O)NH- or -O-(CH2)k-C(=O)NH-. In this case, k is an integer of 0 to 2, and is preferablely 1. "An optionally substituted methylene" is, in particular, a methylene which may be substituted with a halogen atom(s) and/or a C1-4 alkyl group(s), and is preferablely a methylene. "An optionally substituted vinylene" is, in particular, a vinylene which may be substituted with a halogen atom(s) and/or a C1-4 alkyl group(s), and is preferablely a vinylene. "An optionally substituted ethylene" is, in particular, an ethylene which may be substituted with a halogen atom(s) and/or a C1-4 alkyl group(s), and is preferablely an ethylene. R14 is a hydrogen atom, a hydroxyl group, an optionally substituted carboxyl group, an optionally substituted carbamoyl group, an optionally substituted C1-6 alkyl group, an optionally substituted C3-C12 cycloalkyl group, an optionally substituted C1-6 alkenyl group, an optionally substituted C1-6 alkynyl group, an optionally substituted C6-C12 aryl group, an optionally substituted (C6-C12)aryl-(C1 -4)alkyl group, -OR17 or -N(R18)R19. R14 is preferablely a hydrogen atom, a hydroxyl group, a carboxyl group which may be substituted with a C1-4 alkyl group, a carbamoyl group which may be substituted with a C1-4 alkyl group, a C1-6 alkyl group which may be substituted with a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a C3-C8 cycloalkyl group which may be substituted with a C1- 4 alkyl group, a phenyl group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a benzyl group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, - OR17 or -N(R18)R19. R14 is more preferablely a hydrogen atom, a hydroxyl group, a carboxyl group, a carbamoyl group, a C1-6 alkyl group which may be substituted with a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a C3-C8 cycloalkyl group, a phenyl group which may be substituted with a hydroxyl group or a carboxyl group, a benzyl group which may be substituted with a hydroxyl group or a carboxyl group, -OR17 or -N(R18)R19. In "-OR17", R17 is an optionally substituted C1-6 alkyl group or an optionally substituted C3-C6 cycloalkyl group. R17 is preferablely a C1-4 alkyl group. In this case, "an optionally substituted C1-6 alkyl group" is, in particular, a C1-6 alkyl group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s), and is preferablely a C1-6 alkyl group. "An optionally substituted C3-6 cycloalkyl group" is, in particular, a C3-6 cycloalkyl group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s), and is preferablely a C3-6 cycloalkyl group. In "-N(R18)R19", R18 and R19 are each independently selected from the group consisting of a hydrogen atom, an optionally substituted C1-6 alkyl group, an optionally substituted C3-C6 cycloalkyl group, or R18 and R19 may together form an optionally substituted C3-C12 cycloalkyl group or an optionally substituted 3-12 membered heterocyclic group. R18 and R19 are preferablely each independently selected from a hydrogen atom, an optionally substituted C1-6 alkyl group, an optionally substituted C3-C6 cycloalkyl group. R18 and R19 are more preferablely each independently selected from a hydrogen atom or a C1-4 alkyl group. Especially, it is preferred that R18 is a hydrogen atom and R19 is a hydrogen atom, i.e. "- N(R18)R19" represents an amino group. In this case, "an optionally substituted C1-6 alkyl group" is, in particular, a C1-6 alkyl group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s), and is preferablely a C1-6 alkyl group. "An optionally substituted C3-6 cycloalkyl group" is, in particular, a C3-6 cycloalkyl group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s), and is preferablely a C3-6 cycloalkyl group. "An optionally substituted C3-12 cycloalkyl group" is, in particular, a C3-12 cycloalkyl group which may be substituted with a halogen atom(s), a hydroxyl group(s), an amino group(s), a carboxyl group(s) and/or a C1-8 alkoxy group(s), and is preferablely a C3-12 cycloalkyl group. R15 and R16 are each independently selected from the group consisting of a hydrogen atom, an optionally substituted C1-6 alkyl group, an optionally substituted C3-C12 cycloalkyl group, an optionally substituted C6- C12 aryl group, an optionally substituted (C6-C12)aryl-(C1-4)alkyl group, an optionally substituted 3-12 membered heterocyclic group, or R15 and R16 may together form =0. R15 and R16 are preferablely each independently selected from the group consisting of a hydrogen atom, an optionally substituted C1-6 alkyl group, an optionally substituted C3-C12 cycloalkyl group, an optionally substituted C6-C12 aryl group, an optionally substituted (C6-C12)aryl-(C1-4)alkyl group, an optionally substituted 3-12 membered heterocyclic group selected from the group consisting of an aziridine group, an azetidine group, an oxetane group, a pyrrolidine group, a tetrahydrofuran group, a pyrrole group, a furan group, a thiophene group, a pyrazole group, an isoxazole group, an isothiazole group, an imidazole group, an oxazole group, a thiazolegroup, a 1 ,2,5-oxadiazole group, a 1 ,3,4-oxadiazole group, a 1 ,3,4-thiadiazole group, a 1 ,2,4-oxadiazole group, a 1 ,2,4-thiadiazole group, a tetrazole group, a piperidine group, a pyridine group, a pyridazine group, a pyrimidine group, a pyrazine group, a tetrahydropyran group, a pyran group, a thiopyran group, an indole group, a benzofuran group, a benzothiophene group, an indazole group, a benzisoxazole group, a benzisothiazole group, a benzimidazole group, a benzoxazole group, a benzothiazole gorup, a quinoline group, an isoquinoline group, a cinnoline group, a phthalazine group, a quinazoline group, a quinoxaline group, or R15 and R16 may together form =0. R15 and R16 are more preferablely each independently selected from the group consisting of a hydrogen atom, a C1- 6 alkyl group which may be substituted with a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a C3-C8 cycloalkyl group which may be substituted with a C1-4 alkyl group, a phenyl group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a benzyl group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a 3-8 membered heterocyclic group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, wherein said heterocyclic group selected from the group consisting of an oxetane group, a tetrahydrofuran group, a pyrrole group, a furan group, a thiophene group, a pyrazole group, an isoxazole group, an isothiazole group, an oxazole group, a thiazole group, a 1 ,2,5-oxadiazole group, a 1 ,3,4-oxadiazole group, a 1 ,3,4-thiadiazole group, a 1 ,2,4-oxadiazole group, a 1 ,2,4-thiadiazole group, a tetrazole group, a pyridine group, a pyridazine group, a pyrimidine group, a pyrazine group, a tetrahydropyran group, a pyran group, a thiopyran group, or R15 and R16 may together form =0. R15 and R16 are furthermore preferablely each independently selected from the group consisting of a hydrogen atom, a C1-6 alkyl group which may be substituted with a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a C3-C8 cycloalkyl group, a phenyl group which may be substituted with a hydroxyl group or a carboxyl group, a benzyl group which may be substituted with a hydroxyl group or a carboxyl group, a 3-8 membered heterocyclic group selected from the group consisting of a tetrahydrofuran group, a pyrrole group, a furan group, a thiophene group, a pyrazole group, an isoxazole group, an isothiazole group, an oxazole group, a thiazole group, a 1 ,2,5- oxadiazole group, a 1 ,3,4-oxadiazole group, a 1 ,3,4-thiadiazole group, a 1 ,2,4-oxadiazole group, a 1 ,2,4-thiadiazole group, a pyridine group, a tetrahyd ropyran group. Regarding R14, R15 and R16, it is preferred that at least one of R14, R15 or R16 is a hydrogen atom, and/or at least one of R14, R15 or R16 is a su bstituent which have a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group. Also, it is preferred that R14 is a hydroxyl group, and/or one of R15 and R16 is a hydrogen atom and the other is a C1-6 alkyl group substituted with a carboxyl group. Or one of (R15 and R17), (R16 and R17), (R15 and R18), (R16 and R18), (R15 and R19) or (R16 and R19) may together form a 3-12 membered cyclic ring which is selected from the group consisting of an amidine ring, an amine ring, an ether ring, a lactam ring, a lactone ring, an acetal ring, a hemiacetal ring, a carbonate ring, a carbamate ring, an urea ring, combinations thereof. In this case, said cyclic ring is preferablely a lactam ring or a lactone ring, and is more preferablely a lactone ring. In the above fomula I, R1 and R2 are each independently selected from the group consisting of a C1-6 alkyl group optionally substituted with a halogen atom(s), a C3-6 cycloalkyl group optionally substituted with a halogen atom(s), a C2-6 alkenyl group optionally substituted with a halogen atom(s), a C2-6 alkynyl group optionally substituted with a halogen atom(s), or R1 and R2 may together form a C3-8 cycloalkyl group optionally substituted with a halogen atom(s), a C3-8 cycloalkenyl group optionally substituted with a halogen atom(s) or a C3-8 cycloalkylidene group optionally substituted with a halogen atom(s). Preferable R1 is a C1-6 alkyl group, more preferable R1 is a C1-4 alkyl group, and the most preferable R1 is an ethyl group. Preferable R2 is a C1-6 alkyl group, more preferable R2 is a C1-4 alkyl group, and the most preferable R2 is an ethyl group. In the above fomula I, R3, R4, R5 and R6 are each independently selected from a hydrogen atom, a halogen atom, a C1-6 alkyl group optionally substituted with a halogen atom(s) or a C3-6 cycloalkyl group optionally substituted with a halogen atom(s). Preferable R3 is a hydrogen atom or a C1-6 alkyl group, more preferable R3 is a hydrogen atom or a C1-4 alkyl group, and the most preferable R3 is a hydrogen atom or a methyl group. Preferable R4 is a halogen atom or a C1-6 alkyl group, more preferable R4 is a halogen atom or a C1-4 alkyl group, and the most preferable R4 is a chlorine atom or a methyl group. Preferable R5 is a hydrogen atom. Preferable R6 is a halogen atom or a C1-6 alkyl group, more preferable R6 is a halogen atom or a C1-4 alkyl group, and the most preferable R6 is a chlorine atom, a methyl group, an ethyl group, a propyl group or an isopropyl group. When X is -S(O)n-, -NH- or -O-, Q is selected from a methylene which may be substituted an C1-4 alkyl group, an ethylene, a vinylene, an ethynylene, -(CH2)k-NHC(=O)-, -(CH2)k-C(=O)NH-, -(CH2)k-NHC(=O)NH- or -(CH2)k-SO2-; When Q is -O-, -S-, -NH-, -O-(CH2)k-NHC(=O)-, -O-(CH2)k-C(=O)NH- or -O-(CH2)k-NHC(=O)NH-, X is selected from an optionally substituted methylene, an optionally substituted ethylene, an optionally substituted vinylene or an ethynylene.

Examples of the preferred compounds of the present invention are represented as follows. (1) The compound of the above fomula I wherein X is an optionally substituted methylene, an optionally substituted ethylene, an optionally substituted vinylene or an ethynylene; Y is COOR8, CON(R9)R10, S(0)mR11 or a substituent represented by following formula: OR (CH2)a \ R-I2 R-13 R is a hydrogen atom; R12 and R13 are each independently selected from the group consisting of a hydrogen atom, an optionally substituted C1-10 alkyl group, an optionally substituted C3-10 cycloalkyl group, an optionally substituted C1-10 alkenyl group, an optionally substituted C1-10 alkynyl group, or R12 and R13 may together form an optionally substituted C3-10 cycloalkyl group; W is a substituent represented by following formula: /R-14 — Q-(CH2)b— ^R15 Ri6 Q is -O-, a methylene, an ethylene, a vinylene, an ethynylene, - (CH2)k-C(=O)NH- or -O-(CH2)k-C(=O)NH-; R15 and R16 are each independently selected from the group consisting of a hydrogen atom, an optionally substituted C1-6 alkyl group, an optionally substituted C3-C12 cycloalkyl group, an optionally substituted C6- C12 aryl group, an optionally substituted (C6-C12)aryl-(C1-4)alkyl group, an optionally substituted 3-12 membered heterocyclic group selected from the group consisting of an aziridine group, an azetidine group, an oxetane group, a pyrrolidine group, a tetrahydrofuran group, a pyrrole group, a furan group, a thiophene group, a pyrazole group, an isoxazole group, an isothiazole group, an imidazole group, an oxazole group, a thiazolegroup, a 1 ,2,5- oxadiazole group, a 1 ,3,4-oxadiazole group, a 1 ,3,4-thiadiazole group, a 1 ,2,4-oxadiazole group, a 1 ,2,4-thiadiazole group, a tetrazole group, a piperidine group, a pyridine group, a pyridazine group, a pyrimidine group, a pyrazine group, a tetrahydropyran group, a pyran group, a thiopyran group, an indole group, a benzofuran group, a benzothiophene group, an indazole group, a benzisoxazole group, a benzisothiazole group, a benzimidazole group, a benzoxazole group, a benzothiazole gorup, a quinoline group, an isoquinoline group, a cinnoline group, a phthalazine group, a quinazoline group, a quinoxaline group, or R15 and R16 may together form =0; R17 is an optionally substituted C1-6 alkyl group or an optionally substituted C3-C6 cycloalkyl group; R18 and R19 are each independently selected from a hydrogen atom, an optionally substituted C1-6 alkyl group or an optionally substituted C3-C6 cycloalkyl group; or one of (R15 and R17), (R16 and R17), (R15 and R18), (R16 and R18), (R15 and R19) or (R16 and R19) may together form a 3-12 membered cyclic ring which is selected from a lactam ring or a lactone ring; R1 is a C1-6 alkyl group; R2 is a C1 -6 alkyl group; R3 is a hydrogen atom or a C1-6 alkyl group; R4 is a halogen atom or a C1-6 alkyl group; R5 is a hydrogen atom; R6 is a halogen atom or a C1-6 alkyl group.

(2) The compound according to (1 ) wherein X is an ethylene, a vinylene, or an ethynylene; Y is a substituent represented by following formula: OR (CH2)a \ Ri2 R13 R is a hydrogen atom; R12 and R13 are each independently selected from the group consisting of a hydrogen atom, a C1-8 alkyl group which may be substituted with a halogen atom(s), a C3-8 cycloalkyl group which may be substituted with a C1-4 alkyl group, or R12 and R13 are together form a C3-8 cycloalkyl group which may be substituted with a C 1-4 alkyl group; W is a substituent represented by following formula: yRj4 Q— (CH2)b \~R-i5 R16 Q is -O-, a methylene, an ethylene, a vinylene, an ethynylene, - (CH2)k-C(=O)NH- or -O-(CH2)k-C(=O)NH-; b is an integer of 0 to 5; R14 is a hydrogen atom, a hydroxyl group, a carboxyl group which may be substituted with a C1-4 alkyl group, a carbamoyl group which may be substituted with a C1-4 alkyl group, a C1-6 alkyl group which may be substituted with a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a C3-C8 cycloalkyl group which may be substituted with a C1- 4 alkyl group, a phenyl group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a benzyl group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, - OR17 or -N(R18)R19; R15 and R16 are each independently selected from the group consisting of a hydrogen atom, a C1-6 alkyl group which may be substituted with a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a C3-C8 cycloalkyl group which may be substituted with a C1-4 alkyl group, a phenyl group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a benzyl group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a 3-8 membered heterocyclic group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, wherein said heterocyclic group selected from the group consisting of an oxetane group, a tetrahydrofuran group, a pyrrole group, a furan group, a thiophene group, a pyrazole group, an isoxazole group, an isothiazole group, an oxazole group, a thiazole group, a 1 ,2,5-oxadiazole group, a 1 ,3,4- oxadiazole group, a 1 ,3,4-thiadiazole group, a 1 ,2,4-oxadiazole group, a 1 ,2,4-thiadiazole group, a tetrazole group, a pyridine group, a pyridazine group, a pyrimidine group, a pyrazine group, a tetrahydropyran group, a pyran group, a thiopyran group, or R15 and R16 may together form =0; and at least one of R14, R15 or R16 is a hydrogen atom; R17 is a C1-4 alkyl group; R18 and R19 are each independently selected from a hydrogen atom or a C1-4 alkyl group; or one of (R15 and R17), (R16 and R17), (R15 and R18), (R16 and R18), (R15 and R19) or (R16 and R19) may together form a 3-12 membered lactone ring.

(3) The compound according to (2) wherein R12 and R13 are each independently selected from the group consisting of a hydrogen atom, a C1-6 alkyl group which may be substituted with a halogen atom(s), a C3-8 cycloalkyl group which may be substituted with a C1-4 alkyl group, or R12 and R13 are together form a C3-8 cycloalkyl group; W is a substituent represented by following formula: — Q-(CH2)b— f-R15

Q is -O-, -(CH2)k-C(=O)NH- or -O-(CH2)k-C(=O)NH-; b is O, 1 or 2; k is 1 ; R14 is a hydrogen atom, a hydroxyl group, a carboxyl group, a carbamoyl group, a C1-6 alkyl group which may be substituted with a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a C3-C8 cycloalkyl group, a phenyl group which may be substituted with a hydroxyl group or a carboxyl group, a benzyl group which may be substituted with a hydroxyl group or a carboxyl group, -OR17 or -N(R18)R19; R15 and R16 are each independently selected from the group consisting of a hydrogen atom, a C1-6 alkyl group which may be substituted with a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a C3-C8 cycloalkyl group, a phenyl group which may be substituted with a hydroxyl group or a carboxyl group, a benzyl group which may be substituted with a hydroxyl group or a carboxyl group, a 3-8 membered heterocyclic group selected from the group consisting of a tetrahydrofuran group, a pyrrole group, a furan group, a thiophene group, a pyrazole group, an isoxazole group, an isothiazole group, an oxazole group, a thiazole group, a 1 ,2,5-oxadiazole group, a 1 ,3,4-oxadiazole group, a 1 ,3,4- thiadiazole group, a 1 ,2,4-oxadiazole group, a 1 ,2,4-thiadiazole group, a pyridine group, a tetrahydropyran group; and at least one of R14, R15 or R16 is a hydrogen atom; R18 is a hydrogen atom; R19 is a hydrogen atom; or one of (R15 and R17), (R16 and R17), (R15 and R18), (R16 and R18), (R15 and R19) or (R16 and R19) may together form a 3-12 membered lactone ring; R1 is a C1-4 alkyl group; R2 is a C1-4 alkyl group; R3 is a hydrogen atom or a C1-4 alkyl group; R4 is a halogen atom or a C1-4 alkyl group; R5 is a hydrogen atom; R6 is a halogen atom or a C1-4 alkyl group. >

(4) The compound according to (3) wherein R12 and R13 are selected from the group consisting of one of R12 and R13 is a hydrogen atom and the other is a C1- 6 alkyl group, one of R12 and R13 is a hydrogen atom and the other is a C3- 8 cycloalkyl group which may be substituted with a C1-4 alkyl group, both of R12 and R13 are same and a C1-6 alkyl group which may be substituted with a halogen atom(s), or R12 and R13 are together form a C3-10 cycloalkyl group; Q is -O- or -O-(CH2)k-C(=O)NH-; R1 is an ethyl group; R2 is an ethyl group; R3 is a hydrogen atom or a methyl group; R4 is a chlorine atom or a methyl group; R6 is a chlorine atom, a methyl group, an ethyl group, a propyl group or an isopropyl group.

(5) The compound according to (4) selected from the group consisting of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 - Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 -ynyl)- phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 - Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3-methyl-phe nyl]-propyl}-2- methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1-Ethyl-1-[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-butyl)-phenyl]- propyl}-2-methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy- cyclopentyO-vinyll-S-methyl-phenylJ-propyO^-methyl-phenoxyl^ -hydroxy- pentanoic acid, (S )-5-[4-(1-Ethyl-1-{4-[(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentanoic acid, (R)-5- (4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[3-methyl- 4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-eny l)-phenyl]-propyl}- 2-methyl-phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[3-methyl- 4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1 -enyl)-phenyl]-propyl}- 2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-4-(4-{1 -Ethyl-1 -[3-methyl- 4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-eny l)-phenyl]-propyl}- 2-methyl-phenoxy)-3-hydroxy-butyric acid, (R)-4-(4-{1 -Ethyl-1 -[3-methyl-4- ((E)-4,4)4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl) -phenyl]-propyl}-2- methyl-phenoxy)-3-hydroxy-butyric acid, (S)-6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (S)-6-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-6-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl- 1-[3-methyl-4-(4,4)4-trifluoro-3-hydroxy-3-trifluoromethyl-b ut-1-ynyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl- 1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-b ut-1-ynyl)-phenyl]- propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl- 1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluorometh yl-but-1-enyl)- phenyl]-propyl}-2-mθthyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4-{1 - Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl-phenyl]-propyl}-2-methyl- phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy- pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-prop an8-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1-Ethyl-1-[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-meth yl-phenoxy)- propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-phenoxy)-pro pane-1 ,2-diol, 2- (4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro- 3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-me thyl- phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-pr opyl}-2-methyl- phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro- 3-hydroxy-3-trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl- phenoxymethyl)- propane-1 ,3-diol, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl} -2-methyl- phenoxy)-pentanoic acid, 5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- pentanoic acid, 5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanoic acid, 5-[4-(1 -Ethyl-1 -{4- [(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3-methyl-phenyl}-propyl )-2-methyl- phenoxy]-pentanoic acid, 6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- hexanoic acid, 1-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol, (E)-4-[4-(1 -Ethyl-1 -{3- methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1- trifluoro-2-trifluoromethyl-but-3-en-2-ol, (E)-1 -(4-{1 -[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-3-ethyl-pent-1 -en-3-ol, 1 - [(E)-2-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl -propyl}-2- methyl-phenyl)-vinyl]-cyclopentanol, (E)-4-(4-{1-[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-1 ,1 ,1-trifluoro-2- trifluoromethyl-but-3-en-2-ol, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl- pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydr oxy-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(4-{1- Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2- methyl-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-4(R)- hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy- 4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-h ydroxy- pentanoic acid, 5-(2-Chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)- phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl) -phenyl]-1-ethyl- propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(2-Chloro-4-{1 -[3-chloro-4- (3-hydroxy-4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phen oxy)-4(R)- hydroxy-pentanoic acid sodium salt, 4-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)- benzoic acid, (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-p8ntane-1,4- diol, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (R)-5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydro xy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (E)-4-[4-(1 -Ethyl-1 -{3-methyl-4-[(R)-1 -(tetrahydro-furan-2-yl)methoxy]- phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1 -trifluoro-2-trifluoromethyl-but-3-en-2- ol, (S )-5-(4-{1 -Ethyl-1 -[S-methyl^-^EH^^-trifluoro-S-hydroxy-S- trifluoromethyl-but-1 -enyl)-phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4- diol, (E)-4-[4-(1-Ethyl-1-{3-methyl-4-[(S)-1-(tetrahydro-furan-2-y l)methoxy]- phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2- ol, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1-Ethyl-1-[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl} -2,6-dimethyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2,6-dimethyl-p henoxy)-4- hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-θthyl-3-hydroxy-pent-1 - enyl)-3-propyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2-one, (S)-5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3 -propyl-phenyl]- propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)- 5(S)-hydroxy-hexanoic acid, 6(R)-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy- pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl )-tetrahydro- pyran-2-one, (E)-N-(2-Amino-ethyl)-2-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hyd roxy- pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-acet amide, (E)-5- (4-{1 -Ethyl-1 -[4-(3-θthyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl }-2- methyl-phenoxy)-4-oxo-pentanoic acid, 2- (R)- [2-(4-{1 -Ethyl-1 -[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)- acetylaminoj-propionic acid, 2- (S)-[2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)- acetylamino]-3- phenyl-propionic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-oxo-pentanoic acid, 5-(4-{1 - Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl} -2- methyl-phenoxy)-pentane-1 ,4-diol, (R)-5-(2-Chloro-4-{1 -[3-chloro-4-((R)-3- hydroxy-4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phenoxy methyl)- dihydro-furan-2-one, (R)-5-(2-Chloro-4-{1 -[3-chloro-4-((S)-3-hydroxy-4,4- dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phenoxymethyl)-dihy dro-furan-2-one, (R)-5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydro xy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)-dihydro- furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)-dihydro- furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one, (R)-5- (4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl-phenyl]-propyl}-2- methyl-phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl- phenoxymethyl)-dihydro-furan-2-one, (R)-5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1 - methyl-cyclohexyO-prop-i-ynylJ-S-methyl-phenylJ-propyO^-meth yl- phenoxymethyl]-dihydro-furan-2-one, (R)-5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1 - methyl-cyclohexyO-propyll-S-methyl-phenylJ-propyl^-methyl- phenoxymethyl]-dihydro-furan-2-one, (R)-5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1 - methyl-cyclopentyO-prop-i-ynyll-S-methyl-phenylJ-propyl^-met hyl- phenoxymethyl]-dihydro-furan-2-one, (R)-5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1- methyl-cyclopentyO-propyll-S-methyl-phenylJ-propyO^-methyl- phenoxymethyl]-dihydro-furan-2-one, (R)-5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1 - methyl-cyclopropyO-prop-i-ynyll-S-methyl-phenylJ-propyl^-met hyl- phenoxymethyl]-dihydro-furan-2-one, (R)-5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1 - methyl-cyclopropyO-propyll-S-methyl-phenylJ-propyO^-methyl- phenoxymethyl]-dihydro-furan-2-one, (R)-6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl- 1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-pr opyl}-2-methyl- phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl-1 -[4-((S)-3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl- phenoxymethyl)-tetrahydro-pyran-2-one, (S)-5-(4-{1 -[4-((E)-1 ,3-Diethyl-3- hydroxy-pent-1 -enyl)-3-methyl-phenyl]-1-ethyl-propyl}-2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4- ((E)-4,4,5,5,5-pentafluoro-3-hydroxy-3-pentafluoroethyl-pent -1-enyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[3- methyl-4-(2-methyl-propane-2-sulfinylmethyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(2- methyl-propane-2-sulfonylmethyl)-phenyl]-propyl}-2-methyl-ph enoxymethyl)- dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-meth yl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1-[3-methyl-4-(4, 4,4- trifluoro-3-hydroxy-3-trifluoromethyl-butyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- mθthyl-phenoxymθthyl)-dihydro-furan-2τone, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3- ethyl-3-hydroxy-1-methyl-pent-1-enyl)-3-methyl-phenyl]-propy l}-2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-dec-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenox ymethyl)- dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-hept-1 - enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-hex-1 -enyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1-Ethyl-1-[4- ((E)-3-ethyl-3-hydroxy-non-1-enyl)-3-methyl-phenyl]-propyl}- 2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-oct-1-en-4-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-p henoxymethyl)- dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-oct-1 - enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-oct-1 -enyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)- dihydro-furan-2-one, (S)-5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1- enyl)-3-methyl-phenyl]-propyl}-phenoxymethyl)-dihydro-furan- 2-one, (S)-5- (4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-propyl-phenyl]-pro pyl}- 2-methyl-phenoxymethyl)-dihydro-furan-2-one( (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3- ethyl-S-hydroxy-undec-i-enyO-S-methyl-phenyll-propylJ^-methy l- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-undec-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phen oxymethyl)- dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-3-methyl-but-1 - enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-3-propyl-hex-1 -enyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4- ((E)-3-hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-pr opyl}-2-nnethyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1-Ethyl-1~[4-(1-hydroxy- cyclobutylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy mθthyl)- dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-(1 -hydroxy-cyclohexylethynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one, (S)-5- (4-{1 -Ethyl-1 -[4-(1 -hydroxy-cyclopentylethynyO-S-methyl-phenyll-propyl}^- methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-(3-ethyl- 3-hydroxy-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxym ethyl)- dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-3-methyl-but-1 -ynyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-fur an-2-one, (S)- 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-3-propyl-hex-1 -ynyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1-[4-(3- hydroxy-4,4-dimethyl-decyl)-3-methyl-phenyl]-propyl}-2-methy l- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-(3-hyd roxy-4,4- dimethyl-heptyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxyme thyl)-dihydro- furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-nonyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1- Ethyl- 1 -[4-(3-hydroxy-4 ,4-dimethyl-octyl)-3-methyl-phenyl]-propyl}-2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-(3-hyd roxy-4, 4- dimethyl-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phen oxymethyl)- dihydro-furan-2-one, (S)-5-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one, (S)-5- [4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclobutyl)-vinyl]-3-methyl-phenyl}-propyl)- 2-methyl-phenoxymethyl]-dihydro-furan-2-one, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2- (i-hydroxy-cyclohexyO-vinyll-S-methyl-phenylJ-propyO^-methyl - phenoxymethyl]-dihydro-furan-2-one, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1- hydroxy-cyclopentyO-vinyll-S-methyl-phenylJ-propyO^-methyl- phenoxymethyl]-dihydro-furan-2-one, (S)-5-{4-[1-(4-tert-Butylsulfanylmethyl- 3-methyl-phenyl)-1-ethyl-propyl]-2-methyl-phenoxymethyl}-dih ydro-furan-2- one, (S)-6-(4-{1 -Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)- tetrahydro-pyran-2-one, (S)-6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl- phenoxymethyl)-tetrahydro-pyran-2-one, (S)-6-(4-{1 -Ethyl-1 -[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (S)-6-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (S)-6-(4-{1 -Ethyl- 1-[4-((R)-3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-pr opyl}-2-methyl- phenoxymethyl)-tetrahydro-pyran-2-one, (S)-6-(4-{1 -Ethyl-1 -[4-((S)-3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl- phenoxymethyl)-tetrahydro-pyran-2-one.

(6) The compound according to (4) wherein R3 is a hydrogen atom.

(7) The compound according to (6) selected from the group consisting of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1- Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluorome thyl-but-1-ynyl)- phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1- Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3-methyl-phe nyl]-propyl}-2- methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-butyl)-phenyl]- propyl}-2-methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy- cyclopentylJ-vinyll-S-methyl-phenylJ-propyO^-methyl-phenoxyl ^-hydroxy- pentanoic acid, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclohexyO-vinylJ-S- methyl-phenylJ-propyl^-methyl-phenoxyH-hydroxy-pentanoic acid, (R)-5- (4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[3-methyl- 4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-eny l)-phenyl]-propyl}- 2-methyl-phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[3-methyl- 4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-eny l)-phenyl]-propyl}- 2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-4-(4-{1 -Ethyl-1 -[3-methyl- 4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-eny l)-phenyl]-propyl}- 2-methyl-phenoxy)-3-hydroxy-butyric acid, (R)-4-(4-{1 -Ethyl-1 -[3-methyl-4- ((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl) -phenyl]-propyl}-2- methyl-phenoxy)-3-hydroxy-butyric acid, (S)-6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (S)-6-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-6-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl- 1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-b ut-1-ynyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl- 1 -[3-methyl-4-(4,4)4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 -ynyl)-phenyl]- propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl- 1-[3-methyl-4-((E)-4,4)4-trifluoro-3-hydroxy-3-trifluorometh yl-but-1-enyl)- phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4-{1- Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3-methyl-phenyl]- propyl}-2-methyl- phenoxy)-propane-1 ,2-diol, (S )-3-(4-{1 -Ethyl- 1-[4-((E)-3-ethyl-3-hydroxy- pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-prop ane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1-Ethyl-1-[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-nnethyl-phenyl]-propyl}- 2-methyl- phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-i-ynyl)-phenyl]-propyl}-2-meth yl-phenoxy)- propane-i ^-diol. CS^S^^I-Ethyl-i-tS-methyM-^EH^^-trifluoro-S- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-phenoxy)-pro pane-1 ,2-diol, 2- (4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1-Ethyl-1-[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro- 3-hydroxy-3-trifluoromethyl-but-1 -ynyl)-phenyl]-propyl}-2-methyl- phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4 ,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-pr opyl}-2-methyl- phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro- 3-hydroxy-3-trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl- phenoxymethyl)- propane-1 ,3-diol, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl} -2-methyl- phenoxy)-pentanoic acid, 5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- pentanoic acid, 5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanoic acid, 5-[4-(1 -Ethyl-1 -{4- [(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3-methyl-phenyl}-propyl )-2-methyl- phenoxy]-pentanoic acid, 6-(4-{1-Ethyl-1-[3-methyl-4-((E)-4 ,4 ,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- hexanoic acid , 1 -(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl- propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol, (E)-4-[4-(1 -Ethyl-1 -{3- methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1- trifluoro-2-trifluoromethyl-but-3-en-2-ol, (E)-1 -(4-{1 -[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-pent -1-en-3-ol, 1- [(E)-2-(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl-propyl}-2- methyl-phenyl)-vinyl]-cyclopentanol, (E)-4-(4-{1-[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-1 ,1 ,1 -trifluoro-2- trifluoromethyl-but-3-en-2-ol, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl- pentyO-S-methyl-pheny^-propylJ^-methyl-phenoxyJ^CRJ-hydroxy- pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(4-{1- Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2- methyl-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-4(R)- hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy- 4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-h ydroxy- pentanoic acid, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl) - phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl) -phenyl]-1-ethyl- propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(2-Chloro-4-{1-[3-chloro-4- (3-hydroxy-4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phen oxy)-4(R)- hydroxy-pentanoic acid sodium salt, 4-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)- benzoic acid, (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (S)-5-(4-{1-Ethyl-1-[3-methyl-4-(4 ,4 ,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1 -ynyl)-phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4- diol, (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (E)-4-[4-(1 -Ethyl-1 -{3-methyl-4-[(R)-1 -(tetrahydro-furan-2-yl)methoxy]- phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2- ol, (S)-5-(4-{1 -Ethyl-1 -[S-methyl^-CCEJ^^^-trifluoro-S-hydroxy-S- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (E)-4-[4-(1-Ethyl-1-{3-methyl-4-[(S )-1-(tetrahydro-furan-2-yl)methoxy]- phenyl}-propyl)-2-methyl-phenyl]-1,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2- ol, (S )-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-phenoxy)-4-hydroxy-pentanoic acid, (S )-5-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-propyl-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-θthyl-3- hydroxy-pent-1-enyl)-3-propyl-phenyl]-propyl}-2-methyl-pheno xy)-4-hydroxy- pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5(S)-hydroxy-hexanoic acid, 6(R)-(4-{1 - Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-pro pyl}-2- methyl-phenoxymθthyl)-tetrahydro-pyran-2-one, (E)-N-(2-Amino-ethyl)-2-(4- {1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]-propyl}-2- methyl-phenoxy)-acetamide, (E)-5-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent- 1 -enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-oxo-pent anoic acid, 2- (R)- [2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-acetylamino]-propionic acid, 2- (S)-[2-(4-{1 -Ethyl- 1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl }-2-methyl- phenoxy)-acetylamino]-3-phenyl-propionic acid, 5-(4-{1-Ethyl-1-[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)-4- oxo-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol.

(8) The compound according to (4) wherein R4 is a chlorine atom.

(9) The compound according to (8) selected from 5-(2-Chloro-4-{1-[3- chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)-phenyl]-1-ethyl-pro pyl}-phenoxy)- 4(R)-hydroxy-pentanoic acid, 5-(2-Chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4- dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-hydro xy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl- pentyl)-phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-hydroxy-pentan oic acid, 5-(2- Chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)-phenyl]-1 -ethyl- propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt.

(10) The compound according to (4) wherein R6 is a chlorine atom.

(11) The compound according to (10) selected from the group consisting of 5-(2-Chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)- phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(2-Chloro- 4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)-phenyl]-1-� �thyl-propyl}- phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1 -[3- chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)-phenyl]-1-ethyl-pro pyl}-phenoxy)- 4(R)-hydroxy-pentanoic acid, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4- dimethyl-pentyO-phenyll-i-ethyl-propylJ-phenoxyHCRJ-hydroxy- pentanoic acid sodium salt.

(12) The compound according to (4) wherein R6 is a methyl group.

(13) The compound according to (12) selected from the group consisting of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5- (4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 - ynyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4- {1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3-methyl- phenyl]-propyl}- 2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1-Ethyl-1-[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1-Ethyl-1-[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-butyl)-phenyl]- propyl}-2-methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy- cyclopentyO-vinyll-S-methyl-phenylJ-propyl^-methyl-phenoxyl^ -hydroxy- pentanoic acid, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentanoic acid, (R)-5- (4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[3-methyl- 4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-eny l)-phenyl]-propyl}- 2-methyl-phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1-Ethyl-1-[3-methyl- 4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-eny l)-phenyl]-propyl}- 2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-4-(4-{1-Ethyl-1-[3-methyl- 4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-eny l)-phenyl]-propyl}- 2-methyl-phenoxy)-3-hydroxy-butyric acid, (R)-4-(4-{1 -Ethyl-1 -[3-r∏8thyl-4- ((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl) -phenyl]-propyl}-2- methyl-phenoxy)-3-hydroxy-butyric acid, (S)-6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (S)-6-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-6-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl- 1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 -ynyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1-Ethyl- 1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-b ut-1-ynyl)-phenyl]- propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl- 1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluorometh yl-but-1-enyl)- phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4-{1 - Ethyl-1 -[4-(3-θthyl-3-hydroxy-pent-1-ynyl)-3-methyl-phenyl]-propyl }-2-methyl- phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy- pent-1 -enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-(4 ,4 ,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-meth yl-phenoxy)- propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- propane-1 ,2-diol, (S)-3-(4-{1-Ethyl-1-[3-methyl-4-(4 ,4 ,4-trifluoro-3-hydroxy-3- trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-phenoxy)-pro pane-1 ,2-diol, 2- (4-{1 -Ethyl-1 -^-((EJ-S-ethyl-S-hydroxy-pent-i-enyO-S-methyl-phenylj-propy l}- 2-methyl-phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro- 3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-me thyl- phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-pr opyl}-2-methyl- phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro- 3-hydroxy-3-trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl- phenoxynnethyl)- propane-1 ,3-diol, 5-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl} -2-methyl- phenoxy)-pentanoic acid, 5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- pentanoic acid, 5-[4-(1-Ethyl-1-{4-[(E)-2-(1-hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanoic acid, 5-[4-(1 -Ethyl-1 -{4- [(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3-methyl-phenyl}-propyl )-2-methyl- phenoxy]-pentanoic acid, 6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4I4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- hexanoic acid, 1-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol, (E)-4-[4-(1 -Ethyl-1 -{3- methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1- trifluoro-2-trifluoromethyl-but-3-en-2-ol, (E)-1 -(4-{1 -[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-pent -1-en-3-ol, 1- [(E)-2-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl -propyl}-2- methyl-phenyl)-vinyl]-cyclopentanol, (E)-4-(4-{1-[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-1 ,1 ,1-trifluoro-2- trifluoromethyl-but-3-en-2-ol, 5-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl- pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydr oxy-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(4-{1- Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2- methyl-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(4-{1-Ethyl-1-[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-4(R)- hydroxy-pentanoic acid sodium salt, 4-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)- benzoic acid, (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4I4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1 -ynyl)-pheriyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4- diol, (R)-5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydro xy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (E)-4-[4-(1 -Ethyl-1 -{3-methyl-4-[(R)-1 -(tetrahydro-furan-2-yl)methoxy]- phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1 -trifluoro-2-trifluoromethyl-but-3-en-2- ol, (S)-5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydro xy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (EH-[4-(1-Ethyl-1-{3-methyl-4-[(S)-1-(tθtrahyclro-furan-2-y l)methoxy]- phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1 -trifluoro-2-trifluoromethyl-but-3-en-2- ol, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl} -2,6-dimethyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2,6-dimethyl-p henoxy)-4- hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 - 8nyl)-3-propyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-propyl-phenyl]- propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-ph8nyl]-propyl}-2-meth yl-phenoxy)- 5(S)-hydroxy-hexanoic acid, 6(R)-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy- pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl )-tetrahydro- pyran-2-one, (E)-N-(2-Amino-ethyl)-2-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy- pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-acet amide, (E)-5- (4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]-propyl}-2- methyl-phenoxy)-4-oxo-pentanoic acid, 2- (R)- [2-(4-{1 -Ethyl-1 -[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)- acetylamino]-propionic acid, 2- (S)-[2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phθnyl]-propyl}-2-methyl-phθnoxy )-acetylaπnino]-3- phenyl-propionic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-oxo-pentanoic acid, 5-(4-{1- Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2- methyl-phenoxy)-pentane-1 ,4-diol, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)- 4(R)-hydroxy- pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4 ,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(4-{1-Ethyl-1-[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)- 4(R)-hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3- hydroxy-4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phenoxy )-4(R)-hydroxy- pentanoic acid, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl) - phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl) -phenyl]-1-ethyl- propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(2-Chloro-4-{1 -[3-chloro-4- (3-hydroxy-4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phen oxy)-4(R)- hydroxy-pentanoic acid sodium salt, 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-pentyO-S-methyl-phenyll-propylJ^-methyl-phenoxyJ-δ CSJ-hydroxy- hexanoic acid.

(14) The compound according to (4) wherein X is an ethylene.

(15) The compound according to (14) selected from the group consisting of (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-h ydroxy-pentanoic acid, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-phenoxy)-pro pane-1 ,2-diol, 2- (4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifl uoromethyl-butyl)- phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol, 5-(4-{1 -Ethyl-1 - [4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}- 2-methyl- phenoxy)-pentanoic acid, 1-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1- ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol, 2- (R)- [2-(4-{1- Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2- methyl-phenoxy)-acetylamino]-propionic acid, 2- (S)-[2-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)- acetylamino]-3-phenyl-propionic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4, 4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)- 4-oxo- pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol.

(16) The compound according to (4) wherein X is a vinylene.

(17) The compound according to (16) selected from the group consisting of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5- (4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1 -enyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-[4-(1 -Ethyl-1 -{4- [(E)-2-(1-hydroxy-cyclopentyl)-vinyl]-3-methyl-phenyl}-propy l)-2-methyl- phenoxy]-4-hydroxy-pentanoic acid, (S )-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1-hydroxy- cyclohexyO-vinyll-S-methyl-phenylJ-propyO^-methyl-phenoxyl^- hydroxy- pentanoic acid, (R)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one, (R)-5- (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-t rifluoromethyl-but- 1 -enyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one, (R)-5- (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-t rifluoromethyl-but- 1 -enyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-4- (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-t rifluoromethyl-but- 1 -enyl)-phenyl]-propyl}-2-methyl-phenoxy)-3-hydroxy-butyric acid, (R)-4-(4- {1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethy l-but-1 - enyl)-phenyl]-propyl}-2-methyl-phenoxy)-3-hydroxy-butyric acid, (S)-6-(4-{1 - Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluo romethyl-but-1- enyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyr an-2-one, (S)- 6-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3 -trifluoromethyl- but-i-enyO-phθnyll-propylJ^-methyl-phenoxyJ-δ-hydroxy-hexa noic acid, (R)- 6-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3 -trifluoromethyl- but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-tetrahyd ro-pyran-2-one, (R)-6-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydro xy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-5-hydroxy- hexanoic acid, (S)-3-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3 - methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 - Ethyl-1-[4-((E)-3-hydroxy-4,4-dimethyl-pent-1 -enyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxy)-propane-1 ,2-diol, 2-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy- pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl )-propane- 1 ,3-diol, 2-(4-{1-Ethyl-1-[4-((E)-3-hydroxy-4,4-dimethyl-pent-1-enyl)- 3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1- Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluo romethyl-but-1- enyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol, 5-(4-{1 - Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phen yl]-propyl}-2- methyl-phenoxy)-pentanoic acid, 5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-pr opyl}-2-methyl- phenoxy)-pentanoic acid, 5-[4-(1-Ethyl-1-{4-[(E)-2-(1-hydroxy-cyclopentyl)- vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanoic acid, 5-[4-(1 - Ethyl- 1 -{4-[(E)-2-(1 -hydroxy-cyclohexyl)-vinyl]-3-methyl-phenyl}-propyl)-2- methyl-phenoxy]-pentanoic acid, 3-(4-{1-Ethyl-1-[3-methyl-4-((E)-4l4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-pr opyl}-2-methyl- phenyl)-propionic acid, (E)-4-[4-(1-Ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)- butoxy]-phenyl}-propyl)-2-methyl-phenyl]-1 (1 ,1-trifluoro-2-trifluoronnethyl-but- 3-en-2-ol, (E)-1-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-3-ethyl-pent-1-en-3-ol, 1-[(E)-2-(4-{1-[4-(5-Amino- pentyloxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl) -vinyl]- cyclopentanol, (E)-4-(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl- propyl}-2-methyl-phenyl)-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2-ol, 4-(4- {1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-pro pyl}-2- methyl-phenoxymethyl)-benzoic acid, (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxy)-pentane-1 ,4-diol, (E)-4-[4-(1 -Ethyl-1 -{3-methyl-4-[(R)-1 - (tetrahydro-furan-2-yl)methoxy]-phenyl}-propyl)-2-methyl-phe nyl]-1 ,1,1- trifluoro-2-trifluoromethyl-but-3-en-2-ol, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxy)-pentane-1 ,4-diol, (E)-4-[4-(1-Ethyl-1-{3-methyl-4-[(S)-1- (tetrahydro-furan-2-yl)methoxy]-phenyl}-propyl)-2-methyl-phe nyl]-1 ,1 ,1- trifluoro-2-trifluoromethyl-but-3-en-2-ol, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-phenoxy)-4-hyd roxy- pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2,6-dimethyl-phenoxymethyl)-dihydro-f uran-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]- propylJ^.Θ-dimethyl-phenoxyH-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 - [4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-propyl-phenyl]-prop yl}-2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-propyl-phenyl]-propyl}-2-methyl-pheno xy)-4-hydroxy- pentanoic acid, 6(R)-(4-{1 -Ethyl-1 -^-((EJ-S-ethyl-S-hydroxy-pent-i-enyO-S- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-tetrahydro-py ran-2-one, (E)-N-(2-Amino-ethyl)-2-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-acetamide, (E)-5-(4-{1 -Ethyl-1 -[4- (3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-m ethyl-phenoxy)- 4-oxo-pentanoic acid.

(18) The compound according to (4) wherein X is an ethynylene.

(19) The compound according to (18) selected from the group consisting of (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trif luoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-4-hydroxy- pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-6- (4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 - ynyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyr an-2-one, (R)- 6-(4-{1 -Ethyl-1 -[3-methyl-4-(4I4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 - ynyI)-phenyl]-propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyr an-2-one, (R)- 6-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 - ynyl)-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4- {1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl-phenyl]-propyl}-2- methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-pent-1 -ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane- 1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-propane-1 ,2- diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl- but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-propane- 1 ,3-diol.

(20) The compound according to (4) wherein one of R12 and R13 is a hydrogen atom and the other is a C1-6 alkyl group.

(21 ) The compound according to (20) wherein one of R12 and R13 is a hydrogen atom and the other is a tert-butyl group.

(22) The compound according to (21) selected from the group consisting of (S)-5-(4-{1 -Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-3- (4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent- 1-ynyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, 2-(4-{1 -Ethyl-1 -[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxymethyl)-propane-1 ,3-diol, 5-(4-{1-Ethyl-1-[4-(3-hydroxy-4 ,4-dimethyl- pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid, 1-(4-{1- [4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-me thyl-phenyl)- 4,4-dimethyl-pentan-3-ol, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pent anoic acid, 5- (4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-ph enyl]-propyl}-2- methyl-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(4-{1 -Ethyl-1 - [4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}- 2-methyl- phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methylτphenoxy) -4(R)-hydroxy- pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4- dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-hydro xy-pentanoic acid, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl) -phenyl]-1- ethyl-propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(2- Chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)-phenyl]-1 -ethyl- propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(2-Chloro-4-{1 -[3-chloro-4- (3-hydroxy-4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phen oxy)-4(R)- hydroxy-pentanoic acid sodium salt, 6-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)- 5(S)-hydroxy- hexanoic acid, 2- (R)- [2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-acetylamino]-propio nic acid, 2- (S)-[2-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-me thyl-phenyl]- propylJ^-methyl-phenoxyJ-acetylaminol-S-phenyl-propionic acid.

(23) The compound according to (4) wherein both of R12 and R13 are same and a C1-6 alkyl group which may be substituted with a halogen atom(s).

(24) The compound according to (23) wherein R12 is a trifluoromethyl group and R13 are is a trifluoromethyl group.

(25) The compound according to (24) selected from the group consisting of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5- (4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 - ynyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4- {1 -Ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1 -enyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1-Ethyl-1-[3- methyl^-CCEJ^^^-trifluoro-S-hydroxy-S-trifluoromethyl-but-i- enyO-phenyl]- propylJ^-methyl-phenoxyH-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4I4-trifluoro-3-hydroxy-3-trifluoromethyl-butyl) -phenyl]-propyl}-2- methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-[4-(1-Ethyl-1-{4-[(E)-2-(1- hydroxy-cyclopentyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methy l-phenoxy]-4- hydroxy-pentanoic acid, (S)-5-[4-(1 -Ethyl-1-{4-[(E)-2-(1 -hydroxy-cyclohexyl)- vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy- pentanoic acid, (R).5-(4_{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4)4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-4-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoronnethyl-b ut-1 -enyl)-phenyl]- propyl}-2-methyl-phenoxy)-3-hydroxy-butyric acid, (R)-4-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoronnethyl-b ut-1-enyl)-phenyl]- propyl}-2-methyl-phenoxy)-3-hydroxy-butyric acid, (S)-6-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (S)-6-(4-{1 -Ethyl- 1-[3-methyl-4-((E)-4)4,4-trifluoro-3-hydroxy-3-trifluorometh yl-but-1-enyl)- phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-6-(4-{1- Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluorome thyl-but-1-ynyl)- phenyl]-propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-o ne, (R)-6-(4- {1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 -ynyl)- phenyl]-propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-o ne, (R)-6-(4- {1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 -ynyl)- phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4-{1 - Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluo romethyl-but-1- enyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyr an-2-one, (R)- 6-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3 -trifluoromethyl- but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexa noic acid, (S)- 3-(4-{1 -Ethyl-1 -[4-(3-θthyl-3-hydroxy-pent-1-ynyl)-3-methyl-phenyl]-propyl }-2- methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-propane- 1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1- Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluorome thyl-but-1-ynyl)- phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-butyl)-phenyl]- propyl}-2-methyl- phenoxy)-propane-1 ,2-diol, 2-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1- enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-propa ne-1 ,3-diol, 2- (4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 - ynyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 - Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethy l-but-1 - enyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 - Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluorome thyl-butyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol, 5-(4-{1 -Ethyl-1 -[4-((E)-3- ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)- pentanoic acid, 5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4 ,4 ,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-i-enyO-phenyll-propylJ^-methyl-phenoxyJ- pentanoic acid, 5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclopentyl)-vinyl]-3-methyl-phenyl}- propyl)-2-methyl-phenoxy]-pentanoic acid, 5-[4-(1-Ethyl-1-{4-[(E)-2-(1- hydroxy-cyclohexyO-vinylj-S-methyl-phenylJ-propyO^-methyl-ph enoxy]- pentanoic acid, 6-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3 - trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-hexanoic acid, (E)-4-[4-(1 -Ethyl-1 -{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)- 2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2-ol, (E)-1-(4-{1-[4- (5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-methy l-phenyl)-3- ethyl-pent-1-en-3-ol, 1-[(E)-2-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]- 1 -ethyl-propyl}-2-methyl-phenyl)-vinyl]-cyclopentanol, (E)-4-(4-{1 -[4-(5- Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-methyl-p henyl)-1 ,1 ,1- trifluoro-2-trifluoromethyl-but-3-en-2-ol, 4-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phθn oxymethyl)- benzoic acid, (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (S )-5-(4-{1-Ethyl-1-[3-methyl-4-(4 ,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (E)-4-[4-(1 -Ethyl-1 -{3-methyl-4-[(R)-1 -(tetrahydro-furan-2-yl)methoxy]- phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2- ol, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (E)-4-[4-(1 -Ethyl-1-{3-methyl-4-[(S)-1 -(tetrahydro-furan-2-yl)methoxy]- phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2- ol, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl} -2,6-dimethyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2,6-dimethyl-p henoxy)-4- hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1- enyl)-3-propyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-propyl-phenyl]- propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, 6(R)-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl} -2-methyl- phenoxymethyl)-tetrahydro-pyran-2-one, (E)-N-(2-Amino-ethyl)-2-(4-{1 -ethyl- 1-[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl }-2-methyl- phenoxy)-acetamide, (E)-5-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -enyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-oxo-pentanoic acid, 2- (R)- [2- (4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl} -2- methyl-phenoxy)-acetylamino]-propionic acid, 2- (S)-[2-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)- acetylamino]-3-phenyl-propionic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)- 4-oxo- pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-nrιethyl- phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol.

(26) The compound according to (4) wherein Q is -O-.

(27) The compound according to (26) selected from the group consisting of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5- (4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 - ynyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4- {1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-butyl)-phenyl]- propyl}-2-methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy- cyclopentyO-vinylJ-S-methyl-phenylJ-propyl^-methyl-phenoxyl^ -hydroxy- pentanoic acid, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentanoic acid, (R)-5- (4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methy l-phenyl]-propyl}- 2-methyl-phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[3-methyl- 4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-eny l)-phenyl]-propyl}- 2-methyl-phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[3-methyl- 4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-eny l)-phenyl]-propyl}- 2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-4-(4-{1 -Ethyl-1 -[3-methyl- 4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-eny l)-phenyl]-propyl}- 2-methyl-phenoxy)-3-hydroxy-butyric acid, (R)-4-(4-{1 -Ethyl-1 -[3-methyl-4- ((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl) -phenyl]-propyl}-2- methyl-phenoxy)-3-hydroxy-butyric acid, (S)-6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (S)-6-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4)4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-6-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl- 1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-b ut-1-ynyl)-ph8nyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1-Ethyl- 1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-b ut-1-ynyl)-phenyl]- propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4-{1-Ethyl-1-[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl- 1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluorometh yl-but-1-enyl)- phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4-{1 - Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3-methyl-phenyl]-propyl} -2-methyl- phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy- pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-prop ane-1,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-meth yl-phenoxy)- propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyi]-propyl}-2-meth yl-phenoxy)- propane-1 ,2-diol, (S)-3-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3 - trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-phenoxy)-pro pane-1 ,2-diol, 2- (4-{1 -Ethyl-1 -[4-((E)-3-θthyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-pr opyl}- 2-methyl-phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro- 3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-me thyl- phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-pr opyl}-2-methyl- phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro- 3-hydroxy-3-trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl- phenoxymethyl)- propane-1 ,3-diol, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl} -2-methyl- phenoxy)-pentanoic acid, 5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4 ,4 ,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- pentanoic acid, 5-[4-(1-Ethyl-1-{4-[(E)-2-(1-hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanoic acid, 5-[4-(1 -Ethyl-1 -{4- [(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3-methyl-phenyl}-propyl )-2-methyl- phenoxy]-pentanoic acid, 6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- hexanoic acid, 1-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol, (E)-4-[4-(1 -Ethyl-1 -{3- methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1- trifluoro-2-trifluoromethyl-but-3-en-2-ol, (E)-1 -(4-{1 -[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-3-ethyl-pent-1 -en-3-ol, 1 - [(E)-2-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phθnyl]-1-ethy l-propyl}-2- methyl-phenyl)-vinyl]-cyclopentanol, (E)-4-(4-{1 -[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-1 ,1 ,1 -trifluoro-2- trifluoromethyl-but-3-en-2-ol, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl- pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydr oxy-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(4-{1- Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2- methyl-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-4(R)- hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy- 4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-h ydroxy- pentanoic acid, 5-(2-Chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)- phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl) -phenyl]-1-ethyl- propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(2-Chloro-4-{1 -[3-chloro-4- (3-hydroxy-4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phen oxy)-4(R)- hydroxy-pentanoic acid sodium salt, 4-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)- benzoic acid, (R)-5-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3 - trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (R)-5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydro xy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-nnethyl-phenox y)-pentane-1 ,4- diol, (E)-4-[4-(1 -Ethyl-1 -{3-methyl-4-[(R)-1 -(tetrahydro-furan-2-yl)methoxy]- phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2- ol, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1 -enyl)-phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4- diol, (E)-4-[4-(1 -Ethyl-1 -{3-methyl-4-[(S)-1 -(tetrahydro-furan-2-yl)methoxy]- phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2- ol, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1-Ethyl-1-[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl} -2,6-dimethyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2,6-dimethyl-p henoxy)-4- hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 - enyl)-3-propyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-propyl-phenyl]- propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-m8thyl-phenyl]-propyl}-2-meth yl-phenoxy)- 5(S)-hydroxy-hexanoic acid, 6(R)-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy- pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl )-tetrahydro- pyran-2-one, (E)-N-(2-Amino-ethyl)-2-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy- pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-acet amide, (E)-5- (4-{1 -Ethyl-1 -[4-(3-θthyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]-propyl}-2- methyl-phenoxyH-oxo-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)- 4-oxo- pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-pentane-1,4-diol.

(28) The compound according to (4) wherein at least one of R14, R15 or R16 is a substituent which have a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group.

(29) The compound according to (28) selected from the group consisting of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5- (4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 - ynyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4- {1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1-Ethyl-1-[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-butyl)-phenyl]- propyl}-2-methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy- cyclopentyO-vinyll-S-methyl-phenylJ-propyO^-methyl-phenoxyl^ -hydroxy- pentanoic acid, (S )-5-[4-(1-Ethyl-1-{4-[(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentanoic acid, (R)-5- (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-t rifluoromethyl-but- 1 -enyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-4- (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-t rifluoromethyl-but- 1 -enyl)-phenyl]-propyl}-2-methyl-phenoxy)-3-hydroxy-butyric acid, (R)-4-(4- {1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethy l-but-1 - enyl)-phenyl]-propyl}-2-methyl-phenoxy)-3-hydroxy-butyric acid, (S)-6-(4-{1 - Ethyl-1-[3-methyl-4-((E)-4,4)4-trifluoro-3-hydroxy-3-trifluo romethyl-but-1- enyl)-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4- {1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 -ynyl)- phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4-{1- Ethyl-i-tS-methyl^-CCEJ^^^-trifluoro-S-hydroxy-S-trifluorome thyl-but-i- enyl)-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4- {1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl-phenyl]-propyl}-2- methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-propane- 1,2-diol, (S )-3-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1- Ethyl-1-[4-((E)-3-hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl -phenyl]-propyl}- 2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-pr opyl}-2-methyl- phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1 -enyl)-phenyl]-propyl}-2-methyl- phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-ph enoxy)-propane- 1 ,2-diol, 2-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 - [4-((E)-3-hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl] -propyl}-2- methyl-phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-pr opyl}-2-methyl- phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4 ,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-pr opyl}-2-methyl- phenoxymethyl)-propane-1 ,3-diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro- 3-hydroxy-3-trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl- phenoxymethyl)- propane-1 ,3-diol, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl} -2-methyl- phenoxy)-pentanoic acid, 5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- pentanoic acid, 5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanoic acid, 5-[4-(1 -Ethyl-1 -{4- [(E^-CI-hydroxy-cyclohexyO-vinyll-S-methyl-phenylJ-propyl^-m ethyl- phenoxy]-pentanoic acid, 6-(4-{1-Ethyl-1-[3-methyl-4-((E)-4 ,4 ,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- hexanoic acid, 1-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol, (E)-4-[4-(1 -Ethyl-1 -{3- methyl-4-[4-(1 H-tθtrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1- trifluoro-2-trifluoromethyl-but-3-en-2-ol, (E)-1 -(4-{1 -[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-pent -1-en-3-ol, 1- [(E)-2-(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl-propyl}-2- methyl-phenyl)-vinyl]-cyclopentanol, (E)-4-(4-{1-[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-1 ,1 ,1-trifluoro-2- trifluoromethyl-but-3-en-2-ol, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl- pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydr oxy-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4 ,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(4-{1- Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2- methyl-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyi]-propyl}-2-methyl-pheno xy)-4(R)- hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy- 4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-h ydroxy- pentanoic acid, 5-(2-Chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)- phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl) -phenyl]-1-ethyl- propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(2-Chloro-4-{1-[3-chloro-4- (3-hydroxy-4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phen oxy)-4(R)- hydroxy-pentanoic acid sodium salt, 4-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)- benzoic acid, (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1 -ynyl)-phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4- diol, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4 ,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4- diol, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4 ,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1,4- diol, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl} -2,6-dimethyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-propyl-phenyl]-propyl}-2-methyl-pheno xy)-4-hydroxy- pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5(S)-hydroxy-hexanoic acid, (E)-N-(2- Amino-ethyl)-2-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-acetamide, (E)-5-(4-{1 -Ethyl-1 -[4-(3-ethyl- 3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phe noxy)-4-oxo- pentanoic acid, 2- (R)- [2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4 ,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-acetylamino]-propio nic acid, 2- (S)-[2-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-me thyl-phenyl]- propyl}-2-methyl-phenoxy)-acetylamino]-3-phenyl-propionic acid, 5-(4-{1 - Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-nnethyl-phenyl]-propyl }-2- methyl-phenoxy)-4-oxo-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4, 4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)- pentane-1,4- diol.

(30) The compound according to (4) wherein R14 is a hydroxyl group.

(31) The compound according to (30) selected from the group consisting of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5- (4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 - ynyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4- {1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3-methyl-phenyl]-pr opyl}- 2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-butyl)-phenyl]- propyl}-2-methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1-hydroxy- cyclopentyO-vinyll-S-methyl-phenylJ-propyO^-methyl-phenoxyl^ -hydroxy- pentanoic acid, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentanoic acid, (R)-5- (4-{1 -Ethyl-1 -[S-methyl^-CCEH^^-trifluoro-S-hydroxy-S-trifluoromethyl-but - 1 -enyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-4- (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4)4-trifluoro-3-hydroxy-3-t rifluoromethyl-but- 1 -enyl)-phenyl]-propyl}-2-methyl-phenoxy)-3-hydroxy-butyric acid, (R)-4-(4- {1 -Ethyl-1 -[S-methyl^-CCEH^^-trifluoro-S-hydroxy-S-trifluoromethyl-but -i - enyl)-phenyl]-propyl}-2-methyl-phenoxy)-3-hydroxy-butyric acid, (S)-6-(4-{1- Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluo romethyl-but-1- enyl)-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4- {1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 -ynyl)- phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4-{1 - Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethy l-but-1 - enyl)-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4- {1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl-phenyl]-propyl}-2- methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-propane- 1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 - Ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl ]-propyl}- 2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-pr opyl}-2-methyl- phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-pr opyl}-2-methyl- phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-ph enoxy)-propane- 1 ,2-diol, 5-(4-{1 -Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl] - propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(4-{1-Ethyl-1-[4- (3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-m ethyl-phenoxy)- 4(R)-hydroxy-pentanoic acid sodium salt, 5-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)- 4(R)-hydroxy- pentanoic acid, 5-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl) -phenyl]-1-ethyl- propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(2-Chloro-4-{1-[3-chloro-4- (3-hydroxy-4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phen oxy)-4(R)- hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy- 4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-h ydroxy- pentanoic acid, 5-(2-Chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)- phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, (R)-5-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3 -trifluoromethyl- but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol, (S)-5-(4-{1- Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluorome thyl-but-1-ynyl)- phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol, (R)-5-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol, (S)-5-(4-{1-Ethyl-1-[3-methyl-4- ((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl) -phenyl]-propyl}-2- methyl-phenoxy)-pentane-1 ,4-diol, (S)-5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-phenoxy)-4-hyd roxy- pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2,6-dimethyl-phenoxy)-4-hydroxy-penta noic acid, (S)- 5-(4-{1 -Ethyl-1 -[4-((E)-3-θthyl-3-hydroxy-pent-1 -enyl)-3-propyl-phenyl]- propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)- 5(S)-hydroxy-hθxanoic acid, 5-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl- pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol. (32) The compound according to (4) wherein one of R15 and R16 is a hydrogen atom and the other is a C1-6 alkyl group substituted with a carboxyl group.

(33) The compound according to (32) selected from the group consisting of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5- (4-{1 -Ethyl-1 -[3-methyl-4-(4,4)4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 - ynyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4- {1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3~ hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1-Ethyl-1-[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-butyl)-phenyl]- propyl}-2-methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy- cyclopentyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenox y]-4-hydroxy- pentanoic acid, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentanoic acid, (R)-5- (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-t rifluoromethyl-but- 1-enyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoi c acid, (S)-4- (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-t rifluoromethyl-but- 1 -enyl)-phenyl]-propyl}-2-methyl-phenoxy)-3-hydroxy-butyric acid, (R)-4-(4- {1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethy l-but-1 - enyl)-phenyl]-propyl}-2-methyl-phenoxy)-3-hydroxy-butyric acid, (S)-6-(4-{1 - Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluo romethyl-but-1- enyl)-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4- {1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 -ynyl)- phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4-{1- Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluo romethyl-but-1- enyl)-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, 2-(4-{1- Ethyl-1-[3-methyl-4-(4,4,4-trifIuoro-3-hydroxy-3-trifluorome thyl-butyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol, 5-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)- pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid, 5-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxy)-pentanoic acid, 5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1- hydroxy-cyclopentyO-viny∏-S-methyl-phenylJ-propyO^-methyl- phenoxy]- pentanoic acid, 5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanoic acid, 6-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxy)-hexanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)- 4(R)-hydroxy- pentanoic acid, 5-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}- 2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)- 4(R)-hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3- hydroxy-4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phenoxy )-4(R)-hydroxy- pentanoic acid, 5-(2-Chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)- phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt, 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl) -phenyl]-1-ethyl- propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid, 5-(2-Chloro-4-{1 -[3-chloro-4- (3-hydroxy-4,4-dimethyl-pentyl)-phenyl]-1-ethyl-propyl}-phen oxy)-4(R)- hydroxy-pentanoic acid sodium salt, (S )-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-phenoxy)-4-hyd roxy- pentanoic acid, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2,6-dimethyl-phenoxy)-4-hydroxy-penta noic acid, (S)- 5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-propyl-phenyl]- propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)- 5(S)-hydroxy-hexanoic acid.

(34) The compound according to (4) wherein one of (R15 and R17), (R16 and R17), (R15 and R18), (R16 and R18), (R15 and R19) or (R16 and R19) together form a 3-12 membered lactone ring.

(35) The compound according to (34) selected from the group consisting of (R)-5-(2-Chloro-4-{1 -[3-chloro-4-((R)-3-hydroxy-4,4-dimethyl- pentyl)-phenyl]-1 -ethyl-propyl}-phenoxymethyl)-dihydro-furan-2-one, (R)-5- (2-Chloro-4-{1-[3-chloro-4-((S)-3-hydroxy-4,4-dimethyl-penty l)-phenyl]-1- ethyl-propyl}-phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1 -ynyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[4-(3-ethyl-3- hydroxy-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)- dihydro-furan-2-one, (R)-5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-fur an-2-one, (R)- 5-[4-(1-Ethyl-1 -{4-[3-hydroxy-3-(1 -methyl-cyclohexyl)-prop-1 -ynyl]-3-methyl- phenyl}-propyl)-2-methyl-phenoxymethyl]-dihydro-furan-2-one, (R)-5-[4-(1- Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclohexyl)-propyl]-3-meth yl-phenyl}- propyl)-2-methyl-phenoxymethyl]-dihydro-furan-2-one, (R)-5-[4-(1 -Ethyl-1 -{4- [3-hydroxy-3-(1-methyl-cyclopentyl)-prop-1-ynyl]-3-methyl-ph enyl}-propyl)-2- methyl-phenoxymethyl]-dihydro-furan-2-one, (R)-5-[4-(1 -Ethyl-1 -{4-[3- hydroxy-3-(1-methyl-cyclopentyl)-propyl]-3-methyl-phenyl}-pr opyl)-2-methyl- phenoxymethyl]-dihydro-furan-2-one, (R)-5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1 - methyl-cyclopropyO-prop-i-ynyll-S-methyl-phenylJ-propyO^-met hyl- phenoxymethyl]-dihydro-furan-2-one, (R)-5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1 - methyl-cyclopropyO-propylJ-S-methyl-phenylJ-propyO^-methyl- phenoxymethyl]-dihydro-furan-2-one, (R)-6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4)4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifiuoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl- 1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-pr opyl}-2-methyl- phenoxymethyl)-tetrahydro-pyran-2-one, (R)-6-(4-{1 -Ethyl-1 -[4-((S)-3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl- phenoxymethyl)-tetrahydro-pyran-2-one, (S)-5-(4-{1 -[4-((E)-1 ,3-Diethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-1 -ethyl-propyl}-2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4- ((E)-4,4,5,5,5-pentafluoro-3-hydroxy-3-pentafluoroethyl-pent -1-enyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one( (S)-5-(4-{1 -Ethyl-1 -[3- methyl-4-(2-methyl-propane-2-sulfinylmethyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(2- methyl-propane-2-sulfonylmethyl)-phenyl]-propyl}-2-methyl-ph enoxymethyl)- dihydro-furan-2-one, (S )-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-meth yl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4 ,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-butyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S )-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4 ,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3- ethyl-3-hydroxy-1-methyl-pent-1-enyl)-3-methyl-phenyl]-propy l}-2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-dec-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenox ymethyl)- dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-hept-1 - enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-hex-1 -enyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-non-1-enyl)-3-methyl-phenyl]-propyl}- 2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-oct-1-en-4-ynyl)-3-methyl-phenyl]-propyl}-2-nnethyl- phenoxymethyl)- dihydro-furan-2-one, (S)-5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-oct-1- enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-oct-1 -enyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1 -enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)- dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 - enyl)-3-methyl-phenyl]-propyl}-phenoxymethyl)-dihydro-furan- 2-one, (S)-5- (4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-propyl-phenyl]-pro pyl}- 2-methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3- ethyl-3-hydroxy-undec-1-enyl)-3-methyl-phenyl]-propyl}-2-met hyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-undec-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phen oxymethyl)- dihydro-furan-2-one, (S)-5-(4-{1-Ethyl-1-[4-((E)-3-hydroxy-3-methyl-but-1- enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-3-propyl-hex-1 -enyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1-Ethyl-1-[4- ((E)-3-hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-pr opyl}-2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-(1 -hydroxy- cyclobutylethynyO-S-methyl-phenyll-propylJ^-methyl-phenoxyme thyl)- dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-(1 -hydroxy-cyclohexylethynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one, (S)-5- (4-{1 -Ethyl-1 -[4-(1-hydroxy-cyclopentylethynyO-S-methyl-phenylJ-propyl}^- methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-(3-ethyl- 3-hydroxy-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxym ethyl)- dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-3-methyl-but-1 -ynyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-fur an-2-one, (S)- 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-3-propyl-hex-1 -ynyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-decyl)-3-methyl-phenyl]φropyl}-2-methy l- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-heptyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxyme thyl)-dihydro- furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-nonyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1- Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-octyl)-3-methyl-phenyl]-p ropyl}-2-methyl- phenoxymethyl)-dihydro-furan-2-one, (S)-5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phen oxymethyl)- dihydro-furan-2-one, (S)-5-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one, (S)-5- [4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclobutyl)-vinyl]-3-methyl-phenyl}-propyl)- 2-methyl-phenoxymethyl]-dihydro-furan-2-one, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2- (i-hydroxy-cyclohexyO-vinyll-S-methyl-phenylϊ-propyO^-ππe thyl- phenoxymethyl]-dihydro-furan-2-one, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 - hydroxy-cyclopentyO-vinyll-S-methyl-phenylJ-propyO^-methyl- phenoxymethyl]-dihydro-furan-2-one, (S)-5-{4-[1-(4-tert-Butylsulfanylmethyl- 3-methyl-phenyl)-1-ethyl-propyl]-2-methyl-phenoxymethyl}-dih ydro-furan-2- one, (S)-6-(4-{1 -Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)- tetrahydro-pyran-2-one, (S)-6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4 ,4 ,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl- phenoxymethyl)-tetrahydro-pyran-2-one, (S)-6-(4-{1 -Ethyl-1 -[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (S)-6-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one, (S)-6-(4-{1-Ethyl- 1-[4-((R)-3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-pr opyl}-2-methyl- phenoxymethyl)-tetrahydro-pyran-2-one, (S)-6-(4-{1 -Ethyl-1 -[4-((S)-3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl- phenoxymethyl)-tetrahydro-pyran-2-one. (36) The compound according to (3) wherein R12 and R13 are selected from the group consisting of one of R12 and R13 is a hydrogen atom and the other is a C1- 6 alkyl group, one of R12 and R13 is a hydrogen atom and the other is a C3- 8 cycloalkyl group which may be substituted with a C1-4 alkyl group, both of R12 and R13 are same and a C1-6 alkyl group which may be substituted with a halogen atom(s), or R12 and R13 are together form a C3-10 cycloalkyl group; Q is a methylene, an ethylene, an ethynylene or -(CH2)k-C(=O)NH-; R1 is an ethyl group; R2 is an ethyl group; R3 is a hydrogen atom; R4 is a chlorine atom or a methyl group; R6 is a chlorine atom or a methyl group.

(37) The compound according to (36) selected from the group consisting of 3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenyl) -propionic acid, 3- (4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethy l-but- 1-enyl)-phenyl]-propyl}-2-methyl-phenyl)-propionic acid, 6-(4-{1-Ethyl-1-[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenyl)-hex-5-ynoic acid, 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenyl)-h ex-5-ynoic acid, 6-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-(E )- but-1 -enyl)-phenyl]-propyl}-2-methyl-phenyl)-hex-5-ynoic acid, 5-(4-{1 -Ethyl- 1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-( E)-but-1-enyl)- phenyl]-propyl}-2-methyl-phenyl)-pent-4-ynoic acid, 7-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-(E)-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenyl)-hept-6-ynoic acid.

(38) The compound according to (36) wherein R3 is a hydrogen atom. (39) The compound according to (38) selected from the group consisting of 3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1 -ynyl)-phenyl]-propyl}-2-methyl-phenyl)-propionic acid, 3- (4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethy l-but- 1-enyl)-phenyl]-propyl}-2-methyl-phenyl)-propionic acid, 6-(4-{1-Ethyl-1-[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenyl)-hex-5-ynoic acid, 6-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenyl)-h ex-5-ynoic acid, 6-(4-{1 -Ethyl-1 -[3-methyl-4-(4 ,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-(E)- but-1 -enyl)-phenyl]-propyl}-2-methyl-phenyl)-hex-5-ynoic acid, 5-(4-{1 -Ethyl- 1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-( E)-but-1-enyl)- phenyl]-propyl}-2-methyl-phenyl)-pent-4-ynoic acid, 7-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-(E)-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenyl)-hept-6-ynoic acid.

(40) The compound according to (36) wherein R4 is a chlorine atom.

(41) The compound according to (36) wherein R6 is a chlorine atom.

(42) The compound according to (36) wherein R6 is a methyl group.

(43) The compound according to (42) selected from the group consisting of 3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenyl) -propionic acid, 3- (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-t rifluoromethyl-but- 1-enyl)-phenyl]-propyl}-2-methyl-phenyl)-propionic acid, 6-(4-{1-Ethyl-1-[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenyl)-hex-5-ynoic acid, 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenyl)-h ex-5-ynoic acid, 6-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-tri fluoromethyl-(E)- but-1-enyl)-phenyl]-propyl}-2-methyl-phenyl)-hex-5-ynoic acid, 5-(4-{1-Ethyl- 1-[3-methyl-4-(4,4,4-trifluoro~3-hydroxy-3-trifluoronnethyl- (E)-but-1-enyl)- phenyl]-propyl}-2-methyl-phenyl)-pent-4-ynoic acid , 7-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-(E)-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenyl)-hept-6-ynoic acid.

(44) The compound according to (36) wherein X is an ethylene.

(45) The compound according to (44) which is 6-(4-{1-Ethyl-1-[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenyl)-hex- 5-ynoic acid.

(46) The compound according to (36) wherein X is a vinylene.

(47) The compound according to (46) selected from the group consisting of 3-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenyl) -propionic acid, 6-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-tri fluoromethyl-(E)- but-1 -enyl)-phenyl]-propyl}-2-methyl-phenyl)-hex-5-ynoic acid, 5-(4-{1 -Ethyl- 1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-( E)-but-1-enyl)- phenyl]-propyl}-2-methyl-phenyl)-pent-4-ynoic acid, 7-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-(E)-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenyl)-hept-6-ynoic acid.

(48) The compound according to (36) wherein X is an ethynylene.

(49) The compound according to (48) selected from 3-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenyl)-propionic acid or 6-(4-{1-Ethyl-1-[3-methyl-4-(4 ,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-pr opyl}-2-methyl- phenyl)-hex-5-ynoic acid. (50) The compound according to (36) wherein one of R12 and R13 is a hydrogen atom and the other is a C1-6 alkyl group.

(51 ) The compound according to (50) wherein one of R12 and R13 is a hydrogen atom and the other is a tert-butyl group.

(52) The compound according to (51 ) which is 6-(4-{1-Ethyl-1-[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenyl)-hex- 5-ynoic acid.

(53) The compound according to (36) wherein both of R12 and R13 are same and a C1-6 alkyl group which may be substituted with a halogen atom(s).

(54) The compound according to (53) wherein R12 is a trifluoromethyl group and R13 are is a trifluoromethyl group.

(55) The compound according to (54) selected from the group consisting of 3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenyl) -propionic acid, 3- (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-t rifluoromethyl-but- 1 -enyl)-phenyl]-propyl}-2-methyl-phenyl)-propionic acid, 6-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenyl)-hex-5-ynoic acid, 6-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-(E)-but-1-enyl)-phenyl ]-propyl}-2-methyl- phenyl)-hex-5-ynoic acid, 5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-(E)-but-1-enyl)-phenyl]-propyl}-2- methyl-phenyl)- pent-4-ynoic acid, 7-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-(E)-but-1-enyl)-phenyl]-propyl}-2-methyl-phe nyl)-hept-6-ynoic acid.

(56) The compound according to (36) wherein Q is an ethylene. (57) The compound according to (56) selected from 3-(4-{1-Ethyl-1-[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenyl)-propionic acid or 3-(4-{1-Ethyl-1-[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenyl)-propionic acid.

(58) The compound according to (36) wherein Q is an ethynylene.

(59) The compound according to (58) selected from the group consisting of 6-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenyl) -hex-5-ynoic acid, 6-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-tri fluoromethyl-(E)- but-1-enyl)-phenyl]-propyl}-2-methyl-phenyl)-hex-5-ynoic acid, 5-(4-{1-Ethyl- 1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-(E )-but-1 -enyl)- phenyl]-propyl}-2-methyl-phenyl)-pent-4-ynoic acid, 7-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-(E)-bu t-1-enyl)-phenyl]- propyl}-2-methyl-phenyl)-hept-6-ynoic acid, 7-(4-{1-Ethyl-1-[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenyl)-hept-6-ynoic acid, 6-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl- pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenyl)-hex-5-ynoi c acid.

(60) The compound according to (36) wherein at least one of R14, R15 or R16 is a substituent which have a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group.

(61) The compound according to (60) selected from the group consisting of 3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1 -ynyl)-phenyl]-propyl}-2-methyl-phenyl)-propionic acid, 3- (4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethy l-but- 1-enyl)-phenyl]-propyl}-2-methyl-phenyl)-propionic acid, 6-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenyl)-hex-5-ynoic acid, 6-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-(E)-but-1-enyl)-phenyl ]-propyl}-2-methyl- phenyl)-hex-5-ynoic acid, 5-(4-{1-Ethyl-1-[3-methyl-4-(4,4 ,4-trifluoro-3- hydroxy-3-trifluoromethyl-(E)-but-1-enyl)-phenyl]-propyl}-2- methyl-phenyl)- pent-4-ynoic acid, 7-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-(E)-but-1-enyl)-phenyl]-propyl}-2-methyl-phe nyl)-hept-6-ynoic acid, 7-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl- but-1-ynyl)-phenyl]-propyl}-2-methyl-phenyl)-hept-6-ynoic acid, 6-(4-{1 -Ethyl- 1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl }-2-methyl- phenyl)-hex-5-ynoic acid.

(62) The compound according to (36) wherein R14 is a hydroxyl group.

(63) The compound according to (36) wherein one of R15 and R16 is a hydrogen atom and the other is a C1-6 alkyl group substituted with a carboxyl group.

(64) The compound according to (63) selected from the group consisting of 3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenyl) -propionic acid, 3- (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-t rifluoromethyl-but- 1 -enyl)-phenyl]-propyl}-2-methyl-phenyl)-propionic acid, 6-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenyl)-hex-5-ynoic acid, 6-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-(E)-but-1-enyl)-phenyl ]-propyl}-2-methyl- phenyl)-hex-5-ynoic acid, 5-(4-{1-Ethyl-1-[3-methyl-4-(4 ,4 ,4-trifluoro-3- hydroxy-3-trifluoromethyl-(E)-but-1-enyl)-phenyl]-propyl}-2- methyl-phenyl)- pent-4-ynoic acid, 7-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-(E)-but-1-enyl)-phenyl]-propyl}-2-methyl-phe nyl)-hept-6-ynoic acid, 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2-methyl-phenyl)-hex-5-ynoic acid. (65) The compound according to (36) wherein one of (R15 and R17), (R16 and R17), (R15 and R18), (R16 and R18), (R15 and R19) or (R16 and R19) together form a 3-12 membered lactone ring.

Another examples of the preferred compounds of the present invention are represented as follows. (66) The compound of the above fomula I wherein X is an optionally substituted vinylene, or an ethynylene.

(67) The compound of the above fomula I wherein W is a substituent represented by following formula:

Q— (CH2)b v"Ri5

Q is selected from the group consisting of -O-, a methylene, an ethylene, a vinylene, and an ethynylene; and wherein b is 1 ; R14 is a hydroxyl group; R15 is a hydrogen atom; R16 is a C1-6 alkyl group substituted with a carboxyl group.

(68) The compound of the above fomula I selected from the group consisting of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5- (4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 - ynyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-5-(4- {1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl-phenyl]-propyl}-2- methyl-phenoxy)-4-hydroxy-pentanoic acid, (R)-5-(4-{1 -Ethyl-1 -[4-(3~ethyl-3- hydroxy-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-4-hydroxy- pentanoic acid, (S)-6-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6- (4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl-phenyl]-propyl}-2- methyl-phenoxyj-δ-hydroxy-hexanoic acid, (S)-3-(4-{1-Ethyl-1-[4-(3-ethyl-3- hydroxy-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-propane- 1 ,2-diol, 2-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3-methyl- phenyl]- propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol, 4-{1 -Ethyl-1 -[4-(3-8thyl- 3-hydroxy-pent-1 -ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol, 5-(4-{1 - Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3-methyl-phenyl]- propyl}-2-methyl- phenoxy)-pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1-ynyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid, 3-(4-{1 -Ethyl-1 - [4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3-methyl-phenyl]-propyl}- 2-methyl- phenyl)-propionic acid, 1 -(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1- ethyl-propyl}-2-methyl-phenyl)-3-ethyl-pent-1 -yn-3-ol, 3-Ethyl-1 -[4-(1 -ethyl-1 - {3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl-phenyl]- pent-1-yn-3-ol, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (R)-5- (4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-6-(4-{1 -Ethyl-1 -[4-((E)-3- ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)-5- hydroxy-hexanoic acid, (R)-6-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 - enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-h exanoic acid, (S)-3-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, 2-(4-{1 -Ethyl-1 -[4-((E)-3-θthyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)- propane-1 ,3-diol, 4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol, 5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-hexanoic acid, 3-(4-{1 -Ethyl-1 -[4-((E)-3-θthyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheny l)-propionic acid, (E)-1 -(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl-propyl}-2- methyl-phenyl)-3-ethyl-pent-1-en-3-ol, (E)-3-Ethyl-1 -[4-(1 -ethyl-1 -{3-methyl- 4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl-phenyl]-pe nt-1-en-3- ol, (S)-5-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pentyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (R)-5-(4-{1 -Ethyl-1 -[4-(3-ethyl- 3-hydroxy-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy) -4-hydroxy- pentanoic acid, (S)-6-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4-{1 - Ethyl-1-[4-(3-ethyl-3-hydroxy-pθntyl)-3-methyl-phenyl]-prop yl}-2-methyl- phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy- pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, 2-(4- {1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pentyl)-3-methyl-phenyl]-propyl}-2-me thyl- phenoxymethyl)-propane-1 ,3-diol, 4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pentyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenol, 5-(4-{1 -Ethyl-1 -[4-(3-ethyl-3- hydroxy-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-p entanoic acid, 6-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pentyl)-3-methyl-pheny l]-propyl}-2- methyl-phenoxy)-hexanoic acid, 3-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy- pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenyl)-propionic acid, 1 -(4-{1 -[4- (5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-methy l-phenyl)-3- θthyl-pentan-3-ol, 3-Ethyl-1-[4-(1-ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)- butoxy]-phenyl}-propyl)-2-methyl-phenyl]-pentan-3-ol, (R)-5-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-6-(4-{1 -Ethyl-1 -[3- methyl-4-(4)4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phθnoxy)-5-hydroxy-hθxanoic acid, (S)-3-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenoxymethyl)-propane-1 ,3-diol, 4-{1 -Ethyl-1 -[3-methyl-4-(4 ,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-pr opyl}-2-methyl- phenol, 5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1 -ynyl)-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid, 6-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 - ynyl)-phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid, 3-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1- ynyl)-phenyl]- propyl}-2-methyl-phenyl)-propionic acid, 4-(4-{1 -[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-1 ,1 ,1-trifluoro-2- trifluoromethyl-but-3-yn-2-ol, 4-[4-(1 -Ethyl-1 -{3-methyl-4-[4-(1 H-tetrazol-5-yl)- butoxy]-phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but- 3-yn-2-ol, (S)-5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydro xy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-4-hydroxy- pentanoic acid, (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xy)-4-hydroxy- pentanoic acid, (S)-6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xy)-5-hydroxy- hexanoic acid, (R)-6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xy)-5-hydroxy- hexanoic acid, (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1 -enyl)-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2- diol, 2-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)- propane-1 ,3-diol, 4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenol, 5-(4-{1 -Ethyl-1 - [3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl -but-1-enyl)- phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid, 6-(4-{1-Ethyl-1-[3-methyl- 4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-eny l)-phenyl]-propyl}- 2-methyl-phenoxy)-hexanoic acid, 3-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-pr opyl}-2-methyl- phenyl)-propionic acid, (E)-4-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]- 1-ethyl-propyl}-2-methyl-phenyl)-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2- ol, (E)-4-[4-(1 -Ethyl-1 -{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}- propyl)-2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2-ol, (S)-5- (4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifl uoromethyl-butyl)- phenyll-propylJ^-methyl-phenoxyH-hydroxy-pentanoic acid, (R)-5-(4-{1- Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluorome thyl-butyl)-phenyl]- propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-6-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-butyl) -phenyl]-propyl}-2- methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4-{1 -Ethyl-1 -[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-butyl)-phenyl]- propyl}-2-methyl- phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4-{1 -Ethyl-1-[3-methyl-4-(4 ,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-butyl)-phenyl]-propyl} -2-methyl- phenoxy)-propane-1 ,2-diol, 2-(4-{1-Ethyl-1-[3-methyl-4-(4,4 ,4-trifluoro-3- hydroxy-3-trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-ph enoxymethyl)- propane-1 ,3-diol, 4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluorom8thyl-butyl)-phenyl]-propyl}-2-methyl-phenol, 5-(4-{1 -Ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-butyl) -phenyl]-propyl}-2- methyl-phenoxy)-pentanoic acid, 6-(4-{1-Ethyl-1-[3-methyl-4-(4 ,4 ,4-trifluoro- 3-hydroxy-3-trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl- phenoxy)- hexanoic acid, 3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-phenyl)-prop ionic acid, 4-(4- {1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)- 1 ,1 ,1-trifluoro-2-trifluoromethyl-butan-2-ol, 4-[4-(1 -Ethyl-1 -{3-methyl-4-[4-(1 H- tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1 -trifluoro-2- trifluoromethyl-butan-2-ol, (S)-5-(4-{1-Ethyl-1-[4-(3-hydroxy-3-methyl-but-1- ynyO-S-methyl-phenylJ-propyl^-methyl-phenoxyH-hydroxy-pentan oic acid, (R)-5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-3-methyl-but-1 -ynyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-6-(4-{1 -Ethyl-1 -[4- (3-hydroxy-3-methyl-but-1-ynyl)-3-methyl-phenyl]-propyl}-2-m ethyl-phenoxy)- 5-hydroxy-hexanoic acid, (R)-6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-3-methyl-but-1 - ynyO-S-methyl-phenyll-propyl^-methyl-phenoxyJ-δ-hydroxy-hex anoic acid, (S)-3-(4-{1 -Ethyl-1 -[4-(3-hydroxy-3-methyl-but-1 -ynyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, 2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-3- methyl-but-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy methyl)- propane-1 ,3-diol, 4-{1 -Ethyl-1 -[4-(3-hydroxy-3-methyl-but-1-ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol, 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-3-methyl-but- 1 -ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid, 6-(4-{1 - Ethyl-1-[4-(3-hydroxy-3-methyl-but-1-ynyl)-3-methyl-phenyl]- propyl}-2- methyl-phenoxy)-hexanoic acid, 3-(4-{1 -Ethyl-1 -[4-(3-hydroxy-3-methyl-but- 1 -ynyl)-3-methyl-phenyl]-propy|}-2-methyl-phenyl)-propionic acid, 4-(4-{1 -[4- (5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-methy l-phenyl)-2- methyl-but-3-yn-2-ol, 4-[4-(1 -Ethyl-1 -{3-methyl-4-[4-(1 H-tetrazol-5-yl)- butoxy]-phenyl}-propyl)-2-methyl-phenyl]-2-methyl-but-3-yn-2 -ol, (S)-5-(4-{1- Ethyl-1 -[4-((E)-3-hydroxy-3-methyl-but-1 -enyl)-3-methyl-phenyl]-propyl}-2- methyl-phenoxy)-4-hydroxy-pentanoic acid, (R)-5-(4-{1 -Ethyl-1 -[4-((E)-3- hydroxy-3-methyl-but-1-enyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)-4- hydroxy-pentanoic acid, (S)-6-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-3-methyl-but-1 - enyO-S-methyl-phenyll-propylJ^-methyl-phenoxy^δ-hydroxy-hex anoic acid, (R)-6-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-3-methyl-but-1 -enyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4-{1 -Ethyl-1 -[4- ((E)-3-hydroxy-3-methyl-but-1-enyl)-3-methyl-phenyl]-propyl} -2-methyl- phenoxy)-propane-1 ,2-diol, 2-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-3-methyl-but-1 - enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-propa ne-1,3-diol, 4- {1 -Ethyl-1 -[4-((E)-3-hydroxy-3-methyl-but-1 -enyl)-3-methyl-phenyl]-propyl}-2- methyl-phenol, 5-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-3-methyl-but-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid, 6-(4-{1 -Ethyl-1 -[4- ((E)-3-hydroxy-3-methyl-but-1-enyl)-3-methyl-phenyl]-propyl} -2-methyl- phenoxy)-hexanoic acid, 3-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-3-methyl-but-1- enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenyl)-propionic acid, (E)-4-(4-{1- ^-(δ-Amino-pentyloxyJ-S-methyl-phenyll-i-ethyl-propylJ^-met hyl-phenyl)^- methyl-but-3-en-2-ol, (E)-4-[4-(1 -Ethyl-1 -{3-methyl-4-[4-(1 H-tetrazol-5-yl)- butoxy]-phenyl}-propyl)-2-methyl-phenyl]-2-methyl-but-3-en-2 -ol, (S)-5-(4-{1- Ethyl-i-^-CS-hydroxy-S-methyl-butyO-S-methyl-phenylJ-propylJ ^-methyl- phenoxy)-4-hydroxy-pentanoic acid, (R)-5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-3- methyl-butyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-h ydroxy- pentanoic acid, (S)-6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-3-methyl-butyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hθxanoic acid, (R)-6-(4-{1 - Ethyl-1 -[4-(3-hydroxy-3-methyl-butyl)-3-methyl-phenyl]-propyl}-2-me thyl- phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4-{1-Ethyl-1-[4-(3-hydroxy-3- methyl-butyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-pro pane-1 ,2-diol, 2-(4-{1-Ethyl-1-[4-(3-hydroxy-3-methyl-butyl)-3-methyl-pheny l]-propyl}-2- methyl-phenoxymethyl)-propane-1 ,3-diol, 4-{1 -Ethyl-1 -[4-(3-hydroxy-3- methyl-butyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol, 5-(4-{1-Ethyl-1-[4- (3-hydroxy-3-methyl-butyl)-3-methyl-phenyl]-propyl}-2-methyl -phenoxy)- pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-3-methyl-butyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid, 3-(4-{1 -Ethyl-1 -[4-(3- hydroxy-3-methyl-butyl)-3-methyl-phenyl]-propyl}-2-methyl-ph enyl)-propionic acid, 4-(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl-propyl}-2- methyl-phenyl)-2-methyl-butan-2-ol, 4-[4-(1 -Ethyl-1 -{3-methyl-4-[4-(1 H- tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl-phenyl]-2-me thyl-butan-2-ol, (S)-5-(4-{1 -Ethyl-1 -[4-(1 -hydroxy-cyclobutylethynyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (R)-5-(4-{1-Ethyl-1-[4-(1- hydroxy-cyclobutylethynyO-S-methyl-pheny∏-propylJ^-methyl- phenoxyH- hydroxy-pentanoic acid, (S)-6-(4-{1 -Ethyl-1 -[4-(1 -hydroxy-cyclobutylethynyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoi c acid, (R)-6- (4-{1 -Ethyl-1 -[4-(1 -hydroxy-cyclobutylethynyO-S-methyl-phenylj-propyl}^- methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4-{1 -Ethyl-1 -[4-(1-hydroxy- cyclobutylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy )-propane-1 ,2- diol, 2-(4-{1 -Ethyl-1 -[4-(1-hydroxy-cyclobutylethynyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol, 4-{1 -Ethyl-1 -[4-(1 - hydroxy-cyclobutylethynyO-S-methyl-phenylJ-propylJ^-methyl-p henol, 5-(4- {1 -Ethyl-1 -[4-(1 -hydroxy-cyclobutylethynyl)-3-methyl-phenyl]-propyl}-2- methyl-phenoxy)-pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-(1-hydroxy- cyclobutylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy )-hexanoic acid, 3-(4-{1 -Ethyl-1 -[4-(1-hydroxy-cyclobutylethynyl)-3-methyl-phenyl]- propyl}-2-methyl-phenyl)-propionic acid, 1 -(4-{1 -[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1 -ethyl-propylJ^-methyl-phenylethynyO-cyclobutanol, 1 -[4-(1 - Ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl- phenylethynyl]-cyclobutanol, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy- cyclobutyO-vinylJ-S-methyl-phenylJ-propyl^-methyl-phenoxyl^- hydroxy- pentanoic acid, (R)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclobutyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentanoic acid, (S)-6- [4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclobutyO-vinylJ-S-methyl-phenylJ-propyl)- 2-methyl-phenoxy]-5-hydroxy-hexanoic acid, (R)-6-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 - hydroxy-cyclobutyO-vinyll-S-methyl-phenylJ-propyl^-methyl-ph enoxyl-δ- hydroxy-hexanoic acid, (S)-3-[4-(1-Ethyl-1-{4-[(E)-2-(1-hydroxy-cyclobutyl)- vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-propane-1 ,2-diol, 2-[4-(1 - Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclobutyl)-vinyl]-3-methyl-phenyl}-propyl)-2- methyl-phenoxymethyl]-propane-1 ,3-diol, 4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy- cyclobutyO-vinyll-S-methyl-phenylJ-propyO^-methyl-phenol, 5-[4-(1-Ethyl-1- {4-[(E)-2-(1-hydroxy-cyclobutyl)-vinyl]-3-methyl-phenyl}-pro pyl)-2-methyl- phenoxy]-pentanoic acid, 6-[4-(1 -Ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclobutyl)- vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-hexanoic acid, 3-[4-(1- Ethyl-1-{4-[(E)-2-(1-hydroxy-cyclobutyl)-vinyl]-3-methyl-phe nyl}-propyl)-2- methyl-phenyl]-propionic acid, 1-[(E)-2-(4-{1-[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1 -θthyl-propyl}-2-methyl-phenyl)-vinyl]-cyclobutanol, 1 -{(E)-2- [4-(1 -Ethyl-1 -{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2- methyl-phenyl]-vinyl}-cyclobutanol, (S )-5-[4-(1 -Ethyl-1 -{4-[2-(1-hydroxy- cyclobutyO-ethy^-S-methyl-phenylJ-propyO^-methyl-phenoxyl^-h ydroxy- pentanoic acid, (R)-5-[4-(1 -Ethyl-1 -{4-[2-(1 -hydroxy-cyclobutyl)-ethyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentanoic acid, (S)-6- [4-(1 -Ethyl-1 -{4-[2-(1 -hydroxy-cyclobutyO-ethylj-S-methyl-phenylJ-propyl)^- methyl-phenoxy]-5-hydroxy-hexanoic acid, (R)-6-[4-(1 -Ethyl-1 -{4-[2-(1 - hydroxy-cyclobutylJ-ethylJ-S-methyl-phenylJ-propyO^-methyl-p henoxyl-S- hydroxy-hexanoic acid, (S )-3-[4-(1 -Ethyl- 1-{4-[2-(1-hyd roxy-cyclobutyl )- ethyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-propane-1 ,2-diol, 2-[4-(1- Ethyl-1-{4-[2-(1-hydroxy-cyclobutyl)-ethyl]-3-methyl-phenyl} -propyl)-2-methyl- phenoxymethyl]-propane-1 ,3-diol, 4-(1-Ethyl-1-{4-[2-(1-hydroxy-cyclobutyl)- ethyl]-3-methyl-phenyl}-propyl)-2-methyl-phenol, 5-[4-(1 -Ethyl-1 -{4-[2-(1- hydroxy-cyclobutylJ-θthyll-S-methyl-phenylJ-propyl^-methyl- phenoxy]- pentanoic acid, 6-[4-(1-Ethyl-1-{4-[2-(1-hydroxy-cyclobutyl)-ethyl]-3-methyl - phenyl}-propyl)-2-methyl-phenoxy]-hexanoic acid, 3-[4-(1 -Ethyl-1 -{4-[2-(1- hydroxy-cyclobutyl)-ethyl]-3-methyl-phenyl}-propyl)-2-methyl -phenyl]- propionic acid, 1 -[2-(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl- propyl}-2-methyl-phenyl)-ethyl]-cyclobutanol, 1-{2-[4-(1 -Ethyl-1 -{3-methyl-4- [4-(1H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl-pheny l]-ethyl}- cyclobutanol, (S)-5-(4-{1 -Ethyl-1 -[4-(1 -hydroxy-cyclopentylethynyl)-3-mθthyl- phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (R)-5-(4-{1 - Ethyl-1 -^-(i-hydroxy-cyclopentylethynyO-S-methyl-phenylj-propylJ^-m ethyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-6-(4-{1 -Ethyl-1 -[4-(1 -hydroxy- cyclopentylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenox y)-5-hydroxy- hexanoic acid, (R)-6-(4-{1 -Ethyl-1 -[4-(1-hydroxy-cyclopentylethynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4- {1 -Ethyl-1 -[4-(1 -hydroxy-cyclopentylethynyl)-3-methyl-phenyl]-propyl}-2- methyl-phenoxy)-propane-1 ,2-diol, 2-(4-{1 -Ethyl-1 -[4-(1 -hydroxy- cyclopentylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenox ymethyl)- propane-1 ,3-diol, 4-{1 -Ethyl-1 -[4-(1 -hydroxy-cyclopentylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol, 5-(4-{1 -Ethyl-1 -[4-(1 -hydroxy- cyclop8ntylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenox y)-pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-(1-hydroxy-cyclopentylethynyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-hexanoic acid, 3-(4-{1 -Ethyl-1 -[4-(1 -hydroxy- cyclopentylethynyO-S-methyl-phenylJ-propylJ^-methyl-phenyO-p ropionic acid, 1 -(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl-propyl}-2- methyl-phenylethynyl)-cyclopentanol, 1-[4-(1 -Ethyl-1 -{3-methyl-4-[4-(1 H- tetrazol-δ-yO-butoxyj-phΘnylJ-propyO^-nnethyl-phenylethyny lJ-cyclopentanol, (S)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclopentyl)-vinyl]-3-methyl-phenyl}- propyl)-2-methyl-phenoxy]-4-hydroxy-pentanoic acid, (R)-5-[4-(1 -Ethyl-1 -{4- [(E)-2-(1-hydroxy-cyclopentyl)-vinyl]-3-methyl-phenyl}-propy l)-2-methyl- phenoxy]-4-hydroxy-pentanoic acid, (S)-6-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy- cyclopentylJ-vinyll-S-methyl-phenylJ-propyO^-methyl-phenoxyl -δ-hydroxy- hexanoic acid, (R)-6-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-5-hydroxy-hexanoic acid, (S)-3-[4- (1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclopentyO-vinylj-S-methyl-phenylJ-propyl)- 2-methyl-phenoxy]-propane-1 ,2-diol, 2-[4-(1 -Ethyl-1 -{4-[(E)-2-(1-hydroxy- cyclopentyO-vinyll-S-methyl-phenylJ-propyO^-methyl-phenoxyme thyl]- propane-1 ,3-diol, 4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenol, 5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy- cyclopentyO-vinyQ-S-methyl-phenylJ-propyO^-methyl-phenoxyl-p entanoic acid, 6-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydiOxy-cyclopentyl)-vinyl]-3-methyl- phenyl}-propyl)-2-methyl-phenoxy]-hexanoic acid, 3-[4-(1-Ethyl-1-{4-[(E)-2- (1-hydroxy-cyclopentyl)-vinyl]-3-methyl-phenyl}-propyl)-2-me thyl-phenyl]- propionic acid, 1-[(E)-2-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1- ethyl-propyl}-2-methyl-phenyl)-vinyl]-cyclopentanol, 1 -{(E)-2-[4-(1-Ethyl-1 -{3- methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl-phenyl]- vinyl}-cyclopentanol, (S)-5-[4-(1 -Ethyl-1 -{4-[2-(1-hydroxy-cyclopentyl)-ethyl]- 3-methyi-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentano ic acid, (R)- 5-[4-(1 -Ethyl-1 -{4-[2-(1 -hydroxy-cyclopentyl)-ethyl]-3-methyl-phenyl}-propyl)- 2-methyl-phenoxy]-4-hydroxy-pentanoic acid, (S)-6-[4-(1 -Ethyl-1 -{4-[2-(1 - hydroxy-cyclopentylJ-ethyll-S-mθthyl-phenylJ-propyl^-mΘthy l-phenoxyj-δ- hydroxy-hexanoic acid, (R)-6-[4-(1 -Ethyl-1 -{4-[2-(1-hydroxy-cyclopentyl)- ethy^-S-methyl-phθnylJ-propyl^-methyl-phenoxyl-δ-hydroxy-h exanoic acid, (S)-3-[4-(1 -Ethyl-1 -{4-[2-(1 -hydroxy-cyclopentyl)-ethyl]-3-methyl-phenyl}- propyl)-2-methyl-phenoxy]-propane-1 ,2-diol, 2-[4-(1-Ethyl-1-{4-[2-(1-hydroxy- cyclopentyl)-ethyl]-3-methyl-phenyl}-propyl)-2-methyl-phθno xymethyl]- propane-1 ,3-diol, 4-(1-Ethyl-1-{4-[2-(1-hydroxy-cyclopentyl)-ethyl]-3-methyl- phenyl}-propyl)-2-methyl-phenol, 5-[4-(1-Ethyl-1-{4-[2-(1-hyd roxy- cyclopentyl)-ethyl]-3-methyl-phenyl}-propyl)-2-methyl-phenox y]-pentanoic acid, 6-[4-(1-Ethyl-1-{4-[2-(1-hydroxy-cyclopentyl)-ethyl]-3-methy l-phenyl}- propyl)-2-methyl-phenoxy]-hexanoic acid, 3-[4-(1 -Ethyl-1 -{4-[2-(1 -hydroxy- cyclopentyl)-ethyl]-3-methyl-phenyl}-propyl)-2-methyl-phenyl ]-propionic acid, 1 -[2-(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl-propyl}-2-methyl- phenyl)-ethyl]-cyclopentanol, 1 -{2-[4-(1 -Ethyl-1 -{3-methyl-4-[4-(1 H-tetrazol-5- yl)-butoxy]-phenyl}-propyl)-2-methyl-phenyl]-ethyl}-cyclopen tanol, (S)-5-(4- {1 -Ethyl-1 -[4-(1 -hydroxy-cyclohexylethynylJ-S-methyl-phenyll-propyl}^- methyl-phenoxy)-4-hydroxy-pentanoic acid, (R)-5-(4-{1-Ethyl-1-[4-(1- hydroxy-cyclohexylethynyl)-3-methyl-phenyl]-propyl}-2-methyl -phenoxy)-4- hydroxy-pentanoic acid, (S)-6-(4-{1-Ethyl-1-[4-(1-hydroxy-cyclohexylethynyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoi c acid, (R)-6- (4-{1 -Ethyl-1 -[4-(1 -hydroxy-cyclohexylethynyO-S-methyl-phenyll-propyl}^- methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4-{1 -Ethyl-1 -[4-(1 -hydroxy- cyclohexylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy )-propane-1 ,2- diol, 2-(4-{1-Ethyl-1-[4-(1-hydroxy-cyclohexylethynyl)-3-methyl-ph enyl]- propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol, 4-{1 -Ethyl-1 -[4-(1- hydroxy-cyclohexylethynyO-S-methyl-phenyll-propyl^-methyl-ph enol, 5-(4- {1 -Ethyl-1 -[4-(1 -hydroxy-cyclohexylethynyO-S-methyl-phenyll-propyl}^- methyl-phenoxy)-pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-(1-hyd roxy- cyclohexylethynyO-S-methyl-phenylJ-propylJ^-methyl-phenoxyJ- hexanoic acid, 3-(4-{1 -Ethyl-1 -[4-(1-hydroxy-cyclohexylethynyl)-3-methyl-phenyl]- propyl}-2-methyl-phenyl)-propionic acid, 1-(4-{1-[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenylethynyl)-cyclohexanol, 1 -[4- (1 -Ethyl-1 -{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl- phenylethynyl]-cyclohexanol, (S)-5-[4-(1-Ethyl-1-{4-[(E)-2-(1-hydroxy- cyclohexyO-vinyll-S-methyl-phenylJ-propyl^-methyl-phenoxyl^- hydroxy- pentanoic acid, (R)-5-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclohexyl)-vinyl]-3- methyl-phθnyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentanoi c acid, (S)-6- [4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclohexyl)-vinyl]-3-methyl-phenyl}-propyl)- 2-methyl-phenoxy]-5-hydroxy-h8xanoic acid, (R)-6-[4-(1 -Ethyl-1 -{4-[(E)-2-(1 - hydroxy-cyclohexyO-vinyll-S-methyl-phθnylJ-propyO^-mΘthyl- phenoxyl-δ- hydroxy-hexanoic acid, (S)-3-[4-(1 -Ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclohexyl)- vinyl]-3-methyl-ph8nyl}-propyl)-2-methyl-phenoxy]-propane-1 ,2-diol, 2-[4-(1- Ethyl-i^-KE^-CI-hydroxy-cyclohexylJ-vinyll-S-methyl-phenylJ- propyl)^- methyl-phenoxym8thyl]-propane-1 ,3-diol, 4-(1 -Ethyl-1 -{4-[(E)-2-(1-hydroxy- cyclohexyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenol, 5-[4-(1 -Ethyl-1 - {4-[(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3-methyl-phenyl}-pro pyl)-2-methyl- phenoxy]-pentanoic acid, 6-[4-(1 -Ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclohexyl)- vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-hexanoic acid, 3-[4-(1 - Ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3-methyl-phenyl}-pr opyl)-2- methyl-phenyl]-propionic acid, 1 -[(E)-2-(4-{1 -[4-(5-Amino-pentyloxy)-3- methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-vinyl]-cyclohexanol, 1 -{(E)- 2-[4-(1 -Ethyl-1 -{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2- methyl-phenyl]-vinyl}-cyclohexanol, (S)-5-[4-(1 -Ethyl-1 -{4-[2-(1 -hydroxy- cyclohexyO-ethyll-S-methyl-phenylJ-propyO^-methyl-phenoxyl^- hydroxy- pentanoic acid, (R)-5-[4-(1 -Ethyl-1 -{4-[2-(1 -hydroxy-cyclohexyl)-ethyl]-3- methyl-phenyl}-propyl)-2-methyl-ph8noxy]-4-hydroxy-pentanoic acid, (S)-6- [4-(1 -Ethyl-1 -{4-[2-(1 -hydroxy-cyclohexyl)-ethyl]-3-methyl-phenyl}-propyl)-2- methyl-phenoxy]-5-hydroxy-hexanoic acid, (R)-6-[4-(1 -Ethyl-1 -{4-[2-(1- hydroxy-cyclohexyO-ethy∏-S-methyl-phenylJ-propyO^-methyl-p henoxyl-δ- hydroxy-hexanoic acid, (S)-3-[4-(1 -Ethyl-1 -{4-[2-(1 -hydroxy-cyclohexyl)- ethyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-propane-1 ,2-diol, 2-[4-(1 - Ethyl-1 -{4-[2-(1-hydroxy-cyclohθxyl)-ethyl]-3-r∏θthyl-phenyl}-p ropyl)-2- methyl-phenoxymethyl]-propane-1 ,3-diol, 4-(1 -Ethyl-1 -{4-[2-(1 -hydroxy- cyclohexyl)-ethyl]-3-methyl-phenyl}-propyl)-2-methyl-phenol, 5-[4-(1 -Ethyl-1 - {4-[2-(1-hydroxy-cyclohexyl)-ethyl]-3-methyl-phenyl}-propyl) -2-methyl- phenoxy]-pentanoic acid, 6-[4-(1 -Ethyl-1 -{4-[2-(1 -hydroxy-cyclohexyl)-ethyl]-3-methyl-phenyl}-propyl)- 2-methyl-phenoxy]-hexanoic acid, 3-[4-(1 -Ethyl-1 -{4-[2-(1 -hydroxy- cyclohexyl)-ethyl]-3-methyl-phenyl}-propyl)-2-methyl-phenyl] -propionic acid, 1 -[2-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl-pr opyl}-2-methyl- phenyl)-ethyl]-cyclohexanol, 1 -{2-[4-(1 -Ethyl-1 -{3-methyl-4-[4-(1 H-tetrazol-5- yl)-butoxy]-phenyl}-propyl)-2-methyl-phenyl]-ethyl}-cyclohex anol, (S)-5-(4-{1- Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent- 1 -ynyl)-3-methyl-phenyl]-propyl}-2- methyl-phenoxy)-4-hydroxy-pentanoic acid, (R)-5-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxy)-4-hydroxy-pentanoic acid, (S)-6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phen oxy)-5- hydroxy-hexanoic acid, (R)-6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4 ,4-dimethyl-pent- 1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy -hexanoic acid, (S)-3-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, 2-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxymethyl)-propane-1 ,3-diol, 4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl- pent-1 -ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol, 5-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxy)-pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 - ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid, 3-(4-{1 - Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3-methyl-phenyl]-pr opyl}-2- methyl-phenyl)-propionic acid , 1 -(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl-pent-1 -yn-3-ol, 1-[4-(1- Ethyl-1-{3-methyl-4-[4-(1H-tetrazol-5-yl)-butoxy]-phenyl}-pr opyl)-2-methyl- phenyl]-4,4-dimethyl-pent-1 -yn-3-ol, (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy- 4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl- phenoxy)-4- hydroxy-pentanoic acid, (R)-5-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl- pent-1 -enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy- pentanoic acid, (S )-6-(4-{1-Ethyl-1-[4-((E)-3-hydroxy-4 ,4-dimethyl-pent-1 - θnyO-S-methyl-phenyll-propylJ^-methyl-phenoxyJ-δ-hydroxy-h exanoic acid, (R)-6-(4-{1-Ethyl-1-[4-((E)-3-hydroxy-4,4-dimethyl-pent-1-en yl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid, (S)-3-(4-{1- Ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1 -enyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxy)-propane-1 ,2-diol, 2-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-4 ,4- dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phen oxymethyl)- propane-1 ,3-diol, 4-{1-Ethyl-1-[4-((E)-3-hydroxy-4,4-dimethyl-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol, 5-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy- 4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl- phenoxy)- pentanoic acid, 6-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid , 3-(4-{1 -Ethyl-1 -[4- ((E)-3-hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-pr opyl}-2-methyl- phenyl)-propionic acid, (E)-1-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]- 1-ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl-pent-1-en-3-ol , (E)-1-[4-(1- Ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl- phenyl]-4,4-dimethyl-pent-1-en-3-ol, (S )-5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4 ,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)- 4-hydroxy- pentanoic acid, (R)-5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid, (S)-6- (4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-ph enyl]-propyl}-2- methyl-phenoxy)-5-hydroxy-hexanoic acid, (R)-6-(4-{1 -Ethyl-1 -[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-5-hydroxy- hexanoic acid, (S)-3-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, 2-(4-{1 -Ethyl-1 - [4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}- 2-methyl- phenoxymethyl)-propane-1 ,3-diol, 4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl- pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol, 5-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)- pentanoic acid, 6-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid, 3-(4-{1 -Ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-nnet hyl-phenyl)- propionic acid, 1-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol, 1 -[4-(1 -Ethyl- 1-{3-methyl- 4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2-methyl-phenyl]-4, 4-dimethyl- pentan-3-ol, 4-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenyl)-butane-1 ,2-diol, (S)-3-(4-{1 -Ethyl-1 -[4-((R)- 3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-me thyl-phenoxy)- propane-1 ,2-diol, (R)-3-(4-{1-Ethyl-1-[4-((R)-3-hydroxy-4,4-dimethyl-pentyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, (S)-3-(4-{1 - Ethyl-1-[4-((S)-3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phen yl]-propyl}-2- methyl-phenoxy)-propane-1 ,2-diol, (R)-3-(4-{1 -Ethyl-1 -[4-((S)-3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)- propane-1 ,2- diol, 2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol, 3-(4-{1 -Ethyl- 1-[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)- propane-1 ,2-diol, (S)-5-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol, 1-(4-{1-Ethyl-1- [4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}- 2-methyl- phenyl)-4,4-dimethyl-pentan-3-ol, 1-(4-{1-Ethyl-1-[4-(3-hydroxy-propyl)-3- methyl-phenyl]-propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan- 3-ol, (S)-3-(4- {1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-nnethyl-phenyl]-propyl }-2- methyl-phenoxy)-propane-1 ,2-diol, (R)-3-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)- propane-1 ,2- diol, 4-(4-{1-Ethyl-1-[4-(2-hydroxy-3,3-dimethyl-butoxy)-3-methyl- phenyl]- propyl}-2-methyl-phenyl)-butane-1 ,2-diol, 1-(4-{1 -Ethyl-1 -[4-(3-hydroxy- propyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-3,3-dimet hyl-butan-2-ol, 3-(4-{1-Ethyl-1-[4-(2-hydroxy-3,3-dimethyl-butoxy)-3-methyl- phenyl]-propyl}- 2-methyl-phenyl)-propane-1 ,2-diol, 3-(4-{1 -Ethyl-1 -[4-(2-hydroxy-3, 3- dimethyl-butoxyVS-methyl-phenyll-propylJ^-nnethyl-phenyO-but ane-i ^-diol, 1 -(4-{1 -Ethyl-1-[4-(2-hydroxy-3,3-dimethyl-butoxy)-3-methyl-phenyl] -propyl}- 2-methyl-phenyl)-propane-1 ,2-diol, 1-(4-{1 -Ethyl-1 -[4-(3-hydroxy-butyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-3,3-dimethyl-butan- 2-ol, (E)-4-(4- {1 -Ethyl-1 -[4-(2-hydroxy-3,3-dimethyl-butoxy)-3-methyl-phenyl]-propyl} -2- methyl-phenyl)-but-3-en-2-ol, 3-(4-{1 -Ethyl-1 -[4-(2-hydroxy-3,3-dimethyl- butoxy)-3-methyl-phenyl]-propyl}-2-methyl-phenyl)-butan-1-ol , 1-(4-{1-[4- (2,3-Dihydroxy-propyl)-3-methyl-phenyl]-1-ethyl-propyl}-2-me thyl-phenoxy)- 3,3-dimethyl-butan-2-one, 1-(4-{1-[4-(2,3-Dihydroxy-1-methyl-propyl)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenoxy)-3,3-dimethy l-butan-2-one, 1 -(4-{1 -Ethyl-1 -[4-(3-hydroxy-butyl)-3-methyl-phenyl]-propyl}-2-methyl- phenoxy)-3,3-dimethyl-butan-2-one, 3-(4-{1 -Ethyl-1 -[4-(2-hydroxy-3,3- dimethyl-butyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-p ropane-1 ,2- diol, (E)-1-(4-{1-[4-((S)-2,3-Dihydroxy-propoxy)-3-methyl-phenyl]- 1-ethyl- propyl}-2-methyl-phenyl)-4,4-dimethyl-pent-1 -en-3-one, (E)-1 -(4-{1 -[4-((R)- 2,3-Dihydroxy-propoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-me thyl-phenyl)- 4,4-dimethyl-pent-1 -en-3-one, (S)-3-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-4,4- dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phen oxy)-propane- 1 ,2-diol, (R)-3-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol, 1-(4-{1-[4-((R)- 2,3-Dihydroxy-propoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-me thyl-phenyl)- 4,4-dimethyl-pentan-3-one.

(69) The compound of the above fomula I which is (S)-5-(4-{1 -Ethyl-1 - [4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-prop yl}-2-methyl- phenoxy)-4-hydroxy-pentanoic acid. (70) The compound of the above fomula I which is (S)-5-(4-{1 -Ethyl- 1 - [3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but -1-ynyl)-phenyl]- propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid.

Another examples of the preferred compounds of the present invention are represented as follows. (71) The compound of the above fomula I wherein Y is a substituent represented by following formula: ✓OR — (CH2)a— f-R12 R-13 and R is a protecting group for a hydroxyl group.

(72) The compound according to (71) wherein X is an optionally substituted methylene, an optionally substituted ethylene, an optionally substituted vinylene or an ethynylene; R is a protecting group for a hydroxyl group selected from the group consisting of a methoxymethyl group, a methylthiomethyl group, a (phenyldimethylsilyl)methoxymethyl group, a benzyloxymethyl group, a p- methoxybenzyloxymethyl group, a p-nitrobenzyloxymethyl group, an o- nitrobenzyloxymethyl group, a (4-methoxyphenoxy)methyl group, a guaiacolmethyl group, a t-butoxymethyl group, a 4-pentenyloxymethyl group, a siloxymethyl group, a 2-methoxyethoxymethyl group, 2,2,2- trichloroethoxymethyl group, a bis(2-chloroethoxy)methyl group, a 2- (trimethylsilyl)ethoxymethyl group, a menthoxymethyl group, a tetrahydropyranyl group, a 3-bromotetrahydropyranyl group, a tertahydrothiopyranyl group, a 1 -methoxycyclohexyl group, 4- methoxytetrahydrothiopyranyl, a tetrahydrofuranyl group, a tetrahydrothiofuranyl group, a 1-ethoxyethyl group, a 1-(2-chloroethoxy)ethyl group, a 1-[2-(trimethylsilyl)ethoxy]ethyl group, a 1-methyl-1-methoxyethyl group, a 1-methyl- 1 -benzyloxyethyl group, a 1-methyl- 1 -benzyloxy-2- fluoroethyl group, a 1-methyl-1-phenoxyethyl group, a 2,2,2-trichloroethyl group, a 1 ,1-dianisyl-2,2,2-trichloroethyl group, a 2-trimethylsilylethyl group, a 2-(benzylthio)ethyl group, a 2-(phenylselenyl)ethyl group, a t-butyl group, an allyl group, a propargyl group, a p-chlorophenyl group, a p- methoxyphenyl group, a p-nitrophenyl group, a 2,4-dinitrophenyl group, a benzyl group, a p-methoxybenzyl group, a 3,4-dimethoxybenzyl group, an o- nitrophenyl group, a p-nitrophenyl group, a p-halobenzyl group, a 2,6- dichlorobenzyl group, a p-cyanobenzyl group, a p-phenylbenzyl group, a 2,6- difluorobenzyl group, a p-acylaminobenzyl group, a 2-triflluoromethyl benzyl group, a 2-picolyl group, a 4-picolyl group, a 2-quinolinylmethyl group, a triphenylmethyl group, a trimethylsilyl group, a triethylsilyl group, a triisopropylsilyl group, a dimethylisopropylsilyl group, a diethylisopropylsilyl group, a t-butyldimethylsilyl group, a t-buthyld iphenylsilyl group, a tribenzylsilyl group, a triphenylsilyl group, a diphenylmethylsilyl group, a di-t- buthylmethylsilyl group, tris(trimethylsilyl)silyl group, a formyl group, a benzoylformyl group, an acetyl group, a chloroacetyl group, a dichloroacetyl group, a trichloroacetyl group, a methoxyacetyl group, a pivaloyl group, a benzoyl group, a 2,4,6-trimethylbenzoyl group, a methylcarbonyloxy group, a methoxymethylcarbonyloxy group, an ethylcarbonyloxy group, an isobutylcarbonyloxy group, a vinylcarbonyloxy group, an allylcarbonyloxy group, a benzylcarbonyloxy group, a p-methoxybenzylcarbonyloxy group, an allylsulfonyl group, a methanesulfonyl group, a benzylsulfonyl group, a tosyl group, a trifluoromethanesulfonyl group; R12 and R13 are each independently selected from the group consisting of a hydrogen atom, an optionally substituted C1-10 alkyl group, an optionally substituted C3-10 cycloalkyl group, an optionally substituted C1-10 alkenyl group, an optionally substituted C1-10 alkynyl group, or R12 and R13 may together form an optionally substituted C3-10 cycloalkyl group; W is a substituent represented by following formula:

-Q-(CH2)b— ^R15 Ri6 Q is -O-, a methylene, an ethylene, a vinylene, an ethynylene, - (CH2)k-C(=O)NH- or -O-(CH2)k-C(=O)NH-; R14 is a hydrogen atom, a hydroxyl group, an optionally substituted carboxyl group, an optionally substituted carbamoyl group, an optionally substituted C1-6 alkyl group, an optionally substituted C3-C12 cycloalkyl group, an optionally substituted G6-C12 aryl group, an optionally substituted (C6-C12)aryl-(C1 -4)alkyl group, -OR17 or -N(R18)R19; R15 and R16 are each independently selected from the group consisting of a hydrogen atom, an optionally substituted C1-6 alkyl group, an optionally substituted C3-C12 cycloalkyl group, an optionally substituted C6- C12 aryl group, an optionally substituted (C6-C12)aryl-(C1-4)alkyl group, an optionally substituted 3-12 membered heterocyclic group selected from the group consisting of an aziridine group, an azetidine group, an oxetane group, a pyrrolidine group, a tetrahydrofuran group, a pyrrole group, a furan group, a thiophene group, a pyrazole group, an isoxazole group, an isothiazole group, an imidazole group, an oxazole group, a thiazolegroup, a 1 ,2,5- oxadiazole group, a 1 ,3,4-oxadiazole group, a 1 ,3,4-thiadiazole group, a 1 ,2,4-oxadiazole group, a 1 ,2,4-thiadiazole group, a tetrazole group, a piperidine group, a pyridine group, a pyridazine group, a pyrimidine group, a pyrazine group, a tetrahydropyran group, a pyran group, a thiopyran group, an indole group, a benzofuran group, a benzothiophene group, an indazole group, a benzisoxazole group, a benzisothiazole group, a benzimidazole group, a benzoxazole group, a benzothiazole gorup, a quinoline group, an isoquinoline group, a cinnoline group, a phthalazine group, a quinazoline group, a quinoxaline group, or R15 and R16 may together form =0; R17 is an optionally substituted C1-6 alkyl group or an optionally substituted C3-C6 cycloalkyl group; R18 and R19 are each independently selected from a hydrogen atom, an optionally substituted C1-6 alkyl group or an optionally substituted C3-C6 cycloalkyl group; or one of (R15 and R17), (R16 and R17), (R15 and R18), (R16 and R18), (R15 and R19) or (R16 and R19) may together form a 3-12 membered cyclic ring which is selected from a lactam ring or a lactone ring; R1 is a C1-6 alkyl group; R2 is a C1-6 alkyl group; R3 is a hydrogen atom or a C1-6 alkyl group; R4 is a halogen atom or a C1-6 alkyl group; R5 is a hydrogen atom; R6 is a halogen atom or a C1-6 alkyl group.

(73) The compound according to (72) wherein X is an ethylene, a vinylene, or an ethynylene; R is a protecting group for a hydroxyl group selected from the group consisting of a methoxymethyl group, a 2-(trimethylsilyl)ethoxymethyl group, a tetrahydropyranyl group, a benzyl group, a p-methoxybenzyl group, a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a t- buthyldiphenylsilyl group, an acetyl group, a pivaloyl group, a benzoyl group, a methanesulfonyl group, a tosyl group, a trifluoromethanesulfonyl group; R12 and R13 are each independently selected from the group consisting of a hydrogen atom, a C1-8 alkyl group which may be substituted with a halogen atom(s) a C3-8 cycloalkyl group which may be substituted with a C1-4 alkyl group, or R12 and R13 are together form a C3-8 cycloalkyl group which may be substituted with a C1-4 alkyl group; W is a substituent represented by following formula: κR14 Q— (CH2)b \~R-i5 R16 Q is -O-, a methylene, an ethylene, a vinylene, an ethynylene, - (CH2)k-C(=O)NH- or -O-(CH2)k-C(=O)NH-; b is an integer of 0 to 5; R14 is a hydrogen atom, a hydroxyl group, a carboxyl group which may be substituted with a C1-4 alkyl group, a carbamoyl group which may be substituted with a C1-4 alkyl group, a C1-6 alkyl group which may be substituted with a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a C3-C8 cycloalkyl group which may be substituted with a C1- 4 alkyl group, a phenyl group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a benzyl group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, OR17 or -N(R18)R19; R15 and R16 are each independently selected from the group consisting of a hydrogen atom, a C1-6 alkyl group which may be substituted with a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a C3-C8 cycloalkyl group which may be substituted with a C1-4 alkyl group, a phenyl group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a benzyl group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a 3-8 membered heterocyclic group which may be substituted with a C1-4 alkyl group, a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, wherein said heterocyclic group selected from the group consisting of an oxetane group, a tetrahydrofuran group, a pyrrole group, a furan group, a thiophene group, a pyrazole group, an isoxazole group, an isothiazole group, an oxazole group, a thiazole group, a 1 ,2,5-oxadiazole group, a 1 ,3,4- oxadiazole group, a 1 ,3,4-thiadiazole group, a 1 ,2,4-oxadiazole group, a 1 ,2,4-thiadiazole group, a tetrazole group, a pyridine group, a pyridazine group, a pyrimidine group, a pyrazine group, a tetrahydropyran group, a pyran group, a thiopyran group, or R15 and R16 may together form =0; and at least one of R14, R15 or R16 is a hydrogen atom; R17 is a C1-4 alkyl group; R18 and R19 are each independently selected from a hydrogen atom or a C1-4 alkyl group; or one of (R15 and R17), (R16 and R17), (R15 and R18), (R16 and R18), (R15 and R19) or (R16 and R19) may together form a 3-12 membered lactone ring.

(74) The compound according to (73) wherein R12 and R13 are each independently selected from the group consisting of a hydrogen atom, a C1-6 alkyl group which may be substituted with a halogen atom(s), a C3-8 cycloalkyl group which may be substituted with a C1-4 alkyl group, or R12 and R13 are together form a C3-8 cycloalkyl group; W is a substituent represented by following formula:

— Q-(CH2)b-^R15 R16 Q is -O-, -(CH2)k-C(=O)NH- or -O-(CH2)k-C(=O)NH-; b is O, 1 or 2; k is 1 ; R14 is a hydrogen atom, a hydroxyl group, a carboxyl group, a carbamoyl group, a C1-6 alkyl group which may be substituted with a hydroxyl group, a carboxyl group, a carbamoyl group or an amide group, a C3-C8 cycloalkyl group, a phenyl group which may be substituted with a hydroxyl group or a carboxyl group, a benzyl group which may be substituted with a hydroxyl group or a carboxyl group, -OR17 or -N(R18)R19; R15 and R16 are each independently selected from the group consisting of a hydrogen atom, a C1-6 alkyl group which may be substituted with a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group, a C3-C8 cycloalkyl group, a phenyl group which may be substituted with a hydroxyl group or a carboxyl group, a benzyl group which may be substituted with a hydroxyl group or a carboxyl group, a 3-8 membered heterocyclic group selected from the group consisting of a tetrahydrofuran group, a pyrrole group, a furan group, a thiophene group, a pyrazole group, an isoxazole group, an isothiazole group, an oxazole group, a thiazole group, a 1 ,2,5-oxadiazole group, a 1 ,3,4-oxadiazole group, a 1 ,3,4- thiadiazole group, a 1 ,2,4-oxadiazole group, a 1 ,2,4-thiadiazole group, a pyridine group, a tetrahydropyran group; and at least one of R14, R15 or R16 is a hydrogen atom; R18 is a hydrogen atom; R19 is a hydrogen atom; or one of (R15 and R17), (R16 and R17), (R15 and R18), (R16 and R18), (R15 and R19) or (R16 and R19) may together form a 3-12 membered lactone ring; R1 is a C1-4 alkyl group; R2 is a C1 -4 alkyl group; R3 is a hydrogen atom or a C1-4 alkyl group; R4 is a halogen atom or a C1-4 alkyl group; R5 is a hydrogen atom; R6 is a halogen atom or a C1-4 alkyl group.

(75) The compound according to (74) wherein R12 and R13 are selected from the group consisting of one of R12 and R13 is a hydrogen atom and the other is a C1- 6 alkyl group, one of R12 and R13 is a hydrogen atom and the other is a C3- 8 cycloalkyl group which may be substituted with a C1-4 alkyl group, both of R12 and R13 are same and a C1-6 alkyl group which may be substituted with a halogen atom(s), or R12 and R13 are together form a C3-10 cycloalkyl group; Q is -O- or -O-(CH2)k-C(=O)NH-; R1 is an ethyl group; R2 is an ethyl group; R3 is a hydrogen atom or a methyl group; R4 is a chlorine atom or a methyl group; R6 is a chlorine atom, a methyl group, an ethyl group, a propyl group or an isopropyl group.

(76) The compound according to (74) wherein R12 and R13 are selected from the group consisting of one of R12 and R13 is a hydrogen atom and the other is a C1- 6 alkyl group, one of R12 and R13 is a hydrogen atom and the other is a C3- 8 cycloalkyl group which may be substituted with a C1-4 alkyl group, both of R12 and R13 are same and a C1-6 alkyl group which may be substituted with a halogen atom(s), or R12 and R13 are together form a C3-10 cycloalkyl group; Q is a methylene, an ethylene, an ethynylene or -(CH2)k-C(=O)NH-; R1 is an ethyl group; R2 is an ethyl group; R3 is a hydrogen atom; R4 is a chlorine atom or a methyl group; R6 is a chlorine atom or a methyl group.

(77) The compound according to (75) or (76) wherein R3 is a hydrogen atom.

(78) The compound according to (75) or (76) wherein R4 is a chlorine atom.

(79) The compound according to (75) or (76) wherein R6 is a chlorine atom.

(80) The compound according to (75) or (76) wherein R6 is a methyl group.

(81) The compound according to (75) or (76) wherein X is an ethylene.

(82) The compound according to (75) or (76) wherein X is a vinylene.

(83) The compound according to (75) or (76) wherein X is an ethynylene. (84) The compound according to (75) or (76) wherein one of R12 and R13 is a hydrogen atom and the other is a C1-6 alkyl group.

(85) The compound according to (84) wherein one of R12 and R13 is a hydrogen atom and the other is a tert-butyl group.

(86) The compound according to (75) or (76) wherein both of R12 and R13 are same and a C1-6 alkyl group which may be substituted with a halogen atom(s).

(87) The compound according to (86) wherein R12 is a trifluoromethyl group and R13 is a trifluoromethyl group.

(88) The compound according to (75) wherein Q is -O-.

(89) The compound according to (76) wherein Q is an ethylene.

(90) The compound according to (76) wherein Q is an ethynylene.

(91 ) The compound according to (75) or (76) wherein at least one of R14, R15 or R16 is a substituent which have a hydroxyl group, a carboxyl group, a carbamoyl group or an amino group.

(92) The compound according to (75) or (76) wherein R14 is a hydroxyl group.

(93) The compound according to (75) or (76) wherein one of R15 and R16 is a hydrogen atom and the other is a C1-6 alkyl group substituted with a carboxyl group. (94) The compound according to (75) or (76) wherein one of (R15 and R17), (R16 and R17), (R15 and R18), (R16 and R18), (R15 and R19) or (R16 and R19) together form a 3-12 membered lactone ring.

Another examples of the preferred compounds of the present invention are represented as follows. (95) The compound of the above fomula I wherein W is a hydroxyl group, a carboxyl group or a trifluoromethanesulfonyloxy group.

(96) The compound according to (95) wherein X is an optionally substituted methylene, an optionally substituted ethylene, an optionally substituted vinylene or an ethynylene; Y is COOR8, CON(R9)R10, S(0)mR11 or a substituent represented by following formula: DR (CH2)a \ R12 Ri3 R is a hydrogen atom or a protecting group for a hydroxyl group selected from the group consisting of a methoxymethyl group, a methylthiomethyl group, a (phenyldimethylsilyl)methoxymethyl group, a benzyloxymethyl group, a p-methoxybenzyloxymethyl group, a p- nitrobenzyloxymethyl group, an o-nitrobenzyloxymethyl group, a (4- methoxyphenoxy)methyl group, a guaiacolmethyl group, a t-butoxymethyl group, a 4-pentenyloxymethyl group, a siloxymethyl group, a 2- methoxyethoxymethyl group, 2,2,2-trichloroethoxymethyl group, a bis(2- chloroethoxy)methyl group, a 2-(trimethylsilyl)ethoxymethyl group, a menthoxymethyl group, a tetrahydropyranyl group, a 3- bromotetrahydropyranyl group, a tertahydrothiopyranyl group, a 1- methoxycyclohexyl group, 4-methoxytetrahydrothiopyranyl, a tetrahydrofuranyl group, a tetrahydrothiofuranyl group, a 1 -ethoxyethyl group, a 1-(2-chloroethoxy)ethyl group, a 1-[2-(trimethylsilyl)ethoxy]ethyl group, a 1-methyl-1-methoxyethyl group, a 1-methyl-1-benzyloxyethyl group, a 1-methyl-1-benzyloxy-2-fluoroethyl group, a 1-methyl- 1 -phenoxyethyl group, a 2,2,2-trichloroethyl group, a 1 ,1-dianisyl-2,2,2-trichloroethyl group, a 2-trimethylsilylethyl group, a 2-(benzylthio)ethyl group, a 2- (phenylselenyl)ethyl group, a t-butyl group, an allyl group, a propargyl group, a p-chlorophenyl group, a p-methoxyphenyl group, a p-nitrophenyl group, a 2,4-dinitrophenyl group, a benzyl group, a p-methoxybenzyl group, a 3,4- dimethoxybenzyl group, an o-nitrophenyl group, a p-nitrophenyl group, a p- halobenzyl group, a 2,6-dichlorobenzyl group, a p-cyanobenzyl group, a p- phenylbenzyl group, a 2,6-difluorobenzyl group, a p-acylaminobenzyl group, a 2-triflluoromethyl benzyl group, a 2-picolyl group, a 4-picolyl group, a 2- quinolinylmethyl group, a triphenylmethyl group, a trimethylsilyl group, a triethylsilyl group, a triisopropylsilyl group, a dimethylisopropylsilyl group, a diethylisopropylsilyl group, a t-butyldimethylsilyl group, a t-buthyldiphenylsilyl group, a tribenzylsilyl group, a triphenylsilyl group, a diphenylmethylsilyl group, a di-t-buthylmethylsilyl group, tris(trimethylsilyl)silyl group, a formyl group, a benzoylformyl group, an acetyl group, a chloroacetyl group, a dichloroacetyl group, a trichloroacetyl group, a methoxyacetyl group, a pivaloyl group, a benzoyl group, a 2,4,6-trimethylbenzoyl group, a methylcarbonyloxy group, a methoxymethylcarbonyloxy group, an ethylcarbonyloxy group, an isobutylcarbonyloxy group, a vinylcarbonyloxy group, an allylcarbonyloxy group, a benzylcarbonyloxy group, a p- methoxybenzylcarbonyloxy group, an allylsulfonyl group, a methanesulfonyl group, a benzylsulfonyl group, a tosyl group, a trifluoromethanesulfonyl group; R12 and R13 are each independently selected from the group consisting of a hydrogen atom, an optionally substituted C1-10 alkyl group, an optionally substituted C3-10 cycloalkyl group, an optionally substituted C1-10 alkenyl group, an optionally substituted C1-10 alkynyl group, or R12 and R13 may together form an optionally substituted C3-10 cycloalkyl group; R1 is a C1-6 alkyl group; R2 is a C1 -6 alkyl group; R3 is a hydrogen atom or a C1-6 alkyl group; R4 is a halogen atom or a C1-6 alkyl group; R5 is a hydrogen atom; R6 is a halogen atom or a C1-6 alkyl group.

(97) The compound according to (96) wherein X is an ethylene, a vinylene, or an ethynylene; Y is a substituent represented by following formula:

(CH2)a \ R12 R13 R is a hydrogen atom or a protecting group for a hydroxyl group selected from the group consisting of a methoxymethyl group, a 2- (trimethylsilyl)ethoxymethyl group, a tetrahydropyranyl group, a benzyl group, a p-methoxybenzyl group, a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a t-buthyldiphenylsilyl group, an acetyl group, a pivaloyl group, a benzoyl group, a methanesulfonyl group, a tosyl group, a trifluoromethanesulfonyl group; R12 and R13 are each independently selected from the group consisting of a hydrogen atom, a C1-8 alkyl group which may be substituted with a halogen atom(s), a C3-8 cycloalkyl group which may be substituted with a C1-4 alkyl group, or R12 and R13 are together form a C3-8 cycloalkyl group which may be substituted with a C1-4 alkyl group.

(98) The compound according to (97) wherein R12 and R13 are each independently selected from the group consisting of a hydrogen atom, a C1-6 alkyl group which may be substituted with a halogen atom(s), a C3-8 cycloalkyl group which may be substituted with a C1-4 alkyl group, or R12 and R13 are together form a C3-8 cycloalkyl group; R1 is a C1-4 alkyl group; R2 is a C1-4 alkyl group; R3 is a hydrogen atom or a C1-4 alkyl group; R4 is a halogen atom or a C1-4 alkyl group; R5 is a hydrogen atom; R6 is a halogen atom or a C1-4 alkyl group.

(99) The compound according to (98) wherein R12 and R13 are selected from the group consisting of one of R12 and R13 is a hydrogen atom and the other is a C1- 6 alkyl group, one of R12 and R13 is a hydrogen atom and the other is a C3- 8 cycloalkyl group which may be substituted with a C1-4 alkyl group, both of R12 and R13 are same and a C1-6 alkyl group which may be substituted with a halogen atom(s), or R12 and R13 are together form a C3-10 cycloalkyl group; R1 is an ethyl group; R2 is an ethyl group; R3 is a hydrogen atom or a methyl group; R4 is a chlorine atom or a methyl group; R6 is a chlorine atom, a methyl group, an ethyl group, a propyl group or an isopropyl group.

(100) The compound according to (99) wherein W is a carboxyl group.

(101) The compound according to (100) which is 4-{1 -Ethyl-1 -[4-((E)- 3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-me thyl-benzoic acid.

(102) The compound according to (99) or (100) wherein wherein R3 is a hydrogen atom.

(103) The compound according to (99) or (100) wherein R4 is a chlorine atom.

(104) The compound according to (99) or (100) wherein R6 is a chlorine atom. (105) The compound according to (99) or (100) wherein R6 is a methyl group.

(106) The compound according to (99) or (100) wherein X is an ethylene.

(107) The compound according to (99) or (100) wherein X is a vinylene.

(108) The compound according to (99) or (100) wherein X is an ethynylene.

(109) The compound according to (99) or (100) wherein one of R12 and R13 is a hydrogen atom and the other is a C1-6 alkyl group.

(110) The compound according to (109) wherein one of R12 and R13 is a hydrogen atom and the other is a tert-butyl group.

(111 ) The compound according to (99) or (100) wherein both of R12 and R13 are same and a C1-6 alkyl group which may be substituted with a halogen atom(s).

(112) The compound according to (111 ) wherein R12 is a trifluoromethyl group and R13 is a trifluoromethyl group.

Pharmaceutical Use

The compounds of the present invention exhibit VDR modulating activity. Therefore, the compounds and compositions of the present invention are useful as pharmaceuticals, such as, for the treatment of abscess, acne, adhesion, alopecia, Alzheimer's disease, benign prostatic hyperplasia, bone fracture healing, cancer, autoimmune induced diabetes, host-graft rejection, insufficient sebum secretion, insufficient dermal firmness, humoral hypercalcemia, insufficient dermal hydration, leukemia, lupus, multiple sclerosis, osteomalacia, osteoporosis, psoriaticarthritis, psoriasis, renal failure, renal osteodystrophy, rheumatoid arthritis, scleroderma, secondary hyperparathyroidism, systemic lupus erythematosus, and wrinkles, cornea wound, cornea healing, retinopathy, sway, muscle weakness, fall, chronic glomerulonephritis, lupus nephritis, diabetic nephropathy, hypocalcemia, hypoparathyroidism, rickets, osteoarthritis, and the like conditions and diseases. Especially, the compounds and compositions of the present invention are useful as pharmaceuticals for the treatment of benign prostatic hyperplasia, cancer, osteoporosis, psoriasis, secondary hyperparathyroidism, chronic glomerulonephritis, lupus nephritis, diabetic nephropathy, sway, muscle weakness, fall, rheumatoid arthritis and/or osteoarthritis. Among the above mentioned diseases, typical disease subjected to the treatment by the compounds and compositions of the present invention are benign prostatic hyperplasia, cancer, osteoporosis, psoriasis, secondary hyperparathyroidism, chronic glomerulonephritis, lupus nephritis and/or diabetic nephropathy. Certain compounds of the present invention are useful as a synthetic intermediate thereof.

Pharmaceutical Compositions

The compositions of the present invention comprise: (a) a safe and therapeutically effective amount of a compound of the present invention, or its corresponding enantiomer, diastereoisomer or tautomer, or pharmaceutically acceptable salt, or a prodrug thereof; and (b) a pharmaceutically acceptable carrier. The compounds useful in this invention can be formulated into pharmaceutical compositions for use in the treatment of numerous diseases as mentioned above, i.e. prophylaxis, management and treatment of these conditions. Standard pharmaceutical formulation techniques are used, such as those disclosed in Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton, PA. A "safe and therapeutically effective amount" of a compound useful in the present invention is an amount that exhibits VDR modulating activity, in a subject, a tissue, or a cell, and preferably in an animal, more preferably in a mammal, without undue adverse side effects (such as toxicity, irritation, or allergic response), commensurate with a reasonable benefit/risk ratio, when used in the manner of this invention. The specific "safe and therapeutically effective amount" will vary with such factors as the particular condition being treated, the physical condition of the patient, the duration of treatment, the nature of concurrent therapy (if any), the specific dosage form to be used, the carrier employed, the solubility of the compound therein, and the dosage regimen desired for the composition. In addition to the selected compound useful for the present invention, the compositions of the present invention contain a pharmaceutically- acceptable carrier. The term "pharmaceutically-acceptable carrier", as used herein, means one or more compatible solid or liquid filler diluents or encapsulating substances, which are suitable for administration to a mammal. The term "compatible", as used herein, means that the components of the composition are capable of being commingled with the subject compound, and with each other, in a manner such that there is no interaction, which would substantially reduce the pharmaceutical efficacy of the composition under ordinary use situations. Pharmaceutically-acceptable carriers must, of course, be of sufficiently high purity and sufficiently low toxicity to render them suitable for administration preferably to an animal, preferably mammal being treated. Some examples of substances, which can serve as pharmaceutically- acceptable carriers or components thereof, are sugars, such as lactose, glucose and sucrose; starches, such as corn starch and potato starch; cellulose and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose, and methyl cellulose; powdered tragacanth; malt; gelatin; talc; solid lubricants, such as stearic acid and magnesium stearate; calcium sulfate; vegetable oils, such as peanut oil, cottonseed oil, sesame oil, olive oil, corn oil and oil of theobroma; polyols such as propylene glycol, glycerine, sorbitol, mannitol, and polyethylene glycol; alginic acid; emulsifiers, such as the TWEENS; wetting agents, such sodium lauryl sulfate; coloring agents; flavoring agents; tableting agents, stabilizers; antioxidants; preservatives; pyrogen-free water; isotonic saline; and phosphate buffer solutions. The choice of a pharmaceutically-acceptable carrier to be used in conjunction with the subject compound is basically determined by the way the compound is to be administered. If the subject compound is to be injected, the preferred pharmaceutically-acceptable carrier is sterile, physiological saline, with blood-compatible suspending agent, the pH of which has been adjusted to about 7.4. In particular, pharmaceutically-acceptable carriers for systemic administration include sugars, starches, cellulose and its derivatives, malt, gelatin, talc, calcium sulfate, vegetable oils, synthetic oils, polyols, alginic acid, phosphate buffer solutions, emulsifiers, isotonic saline, and pyrogen- free water. Preferred carriers for parental administration include propylene glycol, ethyl oleate, pyrrolidone, ethanol, and sesame oil. The compositions of this invention are preferably provided in unit dosage form. As used herein, a "unit dosage form" is a composition of this invention containing an amount of a compound that is suitable for administration to an animal, preferably mammal subject, in a single dose, according to good medical practice. (The preparation of a single or unit dosage form however, does not imply that the dosage form is administered once per day or once per course of therapy. Such dosage forms are contemplated to be administered once, twice, thrice or more per day, and are expected to be given more than once during a course of therapy, though a single administration is not specifically excluded. The skilled artisan will recognize that the formulation does not specifically contemplate the entire course of therapy and such decisions are left for those skilled in the art of treatment rather than formulation.) The compositions useful for this invention may be in any of a variety of forms, suitable (for example) for oral, nasal, rectal, topical (including transdermal), ocular, intracereberally, intravenous, intramuscular, or parental administration. (The skilled artisan will appreciate that oral and nasal compositions comprise compositions that are administered by inhalation, and made using available methodologies.) Depending upon the particular route of administration desired, a variety of pharmaceutically-acceptable carriers well-known in the art may be used. These include solid or liquid fillers, diluents, hydrotropies, surface-active agents, and encapsulating substances. Optional pharmaceutically-active materials may be included, which do not substantially interfere with the activity of the compound. The amount of carrier employed in conjunction with the compound is sufficient to provide a practical quantity of material for administration per unit dose of the compound. Techniques and compositions for making dosage forms useful in the methods of this invention are described in the following references, all incorporated by reference herein: Modern Pharmaceutics, Chapters 9 and 10 (Banker & Rhodes, editors, 1979); Lieberman et al., Pharmaceutical Dosage Forms: Tablets (1981 ); and Ansel, Introduction to Pharmaceutical Dosage Forms 2d Edition (1976). Various oral dosage forms can be used, including such solid forms as tablets, capsules, granules and bulk powders. These oral forms comprise a safe and effective amount. Tablets can be compressed, tablet triturates, enteric-coated, sugar-coated, film-coated, or multiple-compressed, containing suitable binders, lubricants, diluents, disintegrating agents, coloring agents, flavoring agents, flow-inducing agents, and melting agents. Liquid oral dosage forms include aqueous solutions, emulsions, suspensions, solutions and/or suspensions reconstituted from non- effervescent granules, and effervescent preparations reconstituted from effervescent granules, containing suitable solvents, preservatives, emulsifying agents, suspending agents, diluents, sweeteners, melting agents, coloring agents and flavoring agents. The pharmaceutically-acceptable carrier suitable for the preparation of unit dosage forms for peroral administration is well-known in the art. Tablets typically comprise conventional pharmaceutically-compatible adjuvants as inert diluents, such as calcium carbonate, sodium carbonate, mannitol, lactose and cellulose; binders such as starch, gelatin and sucrose; disintegrates such as starch, alginic acid and croscarmelose; lubricants such as magnesium stearate, stearic acid and talc. Glidants such as silicon dioxide can be used to improve flow characteristics of the powder mixture. Coloring agents, such as the FD&C dyes, can be added for appearance. Sweeteners and flavoring agents, such as aspartame, saccharin, menthol, peppermint, and fruit flavors, are useful adjuvants for chewable tablets. Capsules typically comprise one or more solid diluents disclosed above. The selection of carrier components depends on secondary considerations like taste, cost, and shelf stability, which are not critical for the purposes of the subject invention, and can be readily made by a person skilled in the art. Peroral compositions also include liquid solutions, emulsions, suspensions, and the like. The pharmaceutically-acceptable carriers suitable for preparation of such compositions are well known in the art. Typical components of carriers for syrups, elixirs, emulsions and suspensions include ethanol, glycerol, propylene glycol, polyethylene glycol, liquid sucrose, sorbitol and water. For a suspension, typical suspending agents include methyl cellulose, sodium carboxymethyl cellulose, AVICEL RC-591 , tragacanth and sodium alginate; typical wetting agents include lecithin and polysorbate 80; and typical preservatives include methyl paraben and sodium benzoate. Peroral liquid compositions may also contain one or more components such as sweeteners, flavoring agents and colorants disclosed above. Such compositions may also be coated by conventional methods, typically with pH or time-dependent coatings, such that the subject compound is released in the gastrointestinal tract in the vicinity of the desired topical application, or at various times to extend the desired action. Such dosage forms typically include, but are not limited to, one or more of cellulose acetate phthalate, polyvinylacetate phthalate, hydroxypropyl methyl cellulose phthalate, ethyl cellulose, Eudragit coatings, waxes and shellac. Compositions of the subject invention may optionally include other drug actives. Other compositions useful for attaining systemic delivery of the subject compounds include sublingual, buccal and nasal dosage forms. Such compositions typically comprise one or more of soluble filler substances such as sucrose, sorbitol and mannitol; and binders such as acacia, microcrystalline cellulose, carboxymethyl cellulose and hydroxypropyl methyl cellulose. Glidants, lubricants, sweeteners, colorants, antioxidants and flavoring agents disclosed above may also be included. The compositions of this invention can also be administered topically to a subject in a treatment of dermatological conditions such as psoriasis, e.g., by the direct application or spreading of the composition on the epidermal or epithelial tissue of the subject, or transdermal^ via a "patch". Such compositions include, for example, lotions, creams, solutions, gels and solids. These topical compositions preferably comprise a safe and effective amount. Suitable carriers for topical administration preferably remain in place on the skin as a continuous film, and resist being removed by perspiration or immersion in water. Generally, the carrier is organic in nature and capable of having dispersed or dissolved therein the compound. The carrier may include pharmaceutically-acceptable emollient, emulsifiers, thickening agents, solvents and the like.

Methods of Administration

The compounds and compositions useful in this invention can be administered topically or systemically. Systemic application includes any method of introducing compound into the tissues of the body, e.g., intra- articular, intrathecal, epidural, intramuscular, transdermal, intravenous, intraperitoneal, subcutaneous, sublingual administration, inhalation, rectal, or oral administration. The compounds useful in the present invention are preferably administered orally. The specific dosage of the compound to be administered, as well as the duration of treatment is to be individualized by the treating clinicians. Typically, for a human adult, from about 1 ng/kg to 50 mg/kg, preferably from about 1 ng /kg to about 1 mg/kg, more preferably from about 10 ng/kg to about 100 μg/kg, of selected compound is administered per day. It is understood that these dosage ranges are by way of example only, and that daily administration can be adjusted depending on the factors i.e. type of disease, level of disease, ages of patients, sex of patients, route to be administered, etc. In all of the foregoing, of course, the compounds useful in the present invention can be administered alone or as mixtures, and the compositions may further include additional drugs or excipients as appropriate for the indication.

General Synthetic Method

R

R6 1 2 In the above scheme, the compound of general formula (1 ) obtained by the same procedure as described in WO00/10958 and the corresponding U.S. Patent 6,218,430 B1 may be reacted with trifluoromethanesulfonic acid anhydride in the presence of a base to give a compound of general formula (2) (step 1). Suitable bases for use in the above step 1 include pyridine, 2,6- lutidine, 2,4,6-collidine,N,N-dimethylaminopyridine, imidazole, triethylamine, more preferably pyridine. Suitable solvents for use in the above step 1 include diethyl ether, tetrahydrofuran, dichloromethane, 1 ,2-dichloroethane, chloroform, benzene, toluene, more preferably dichloromethane. The reaction temperature of the above step 1 is in the range from -50 °C to 50 0C, preferably from -20 °C to 30 °C, though it is not specifically limited so far as the reaction proceeds.

R5 step 2 OTf R6 ^TMS 2 3 In the above scheme, the compound of general formula (2) may be reacted with trimethylsilyl acetylene in the presence of a palladium catalyst, copper (I) iodide, and triethyamine to give a compound of general formula (3) (step 2). Suitable palladium catalysts for use in the above step 2 include tetrakis(triphenylphosphine)palladium, Pd(dba)2, Pd2(dba)3-CHCI3, palladium acetate, palladium chloride, [1 ,1'-bis(diphenylphosphino)- ferrocene]palladium dichloride dichloromethane complex, (dba; dibenzylideneacetone) A ligand, such as triphenylphosphine, tributhylphosphine, tricyclohexylphosphine, 1 ,3-bis(diphenylphosphinopropane) or tri-t-buthyl phosphine, may be used in the above step 2 to increase the catalytic activity and/or the reaction selectivity. Suitable solvents for use in the above step 2 include N, N- dimethylformamide, dimethylsulfoxide, N.N-dimethylacetamide, 1 ,3-dimethyl- 2-imidazolidinone, tetrahydrofuran, toluene, acetonitrile, more preferably N,N-dimethylformamide or acetonitrile. The reaction temperature of the above step 2 is in the range from 0 °C to 200 °C, preferably from 20 °C to 150 °C, though it is not specifically limited so far as the reaction proceeds. R1 R5 step 3

TMS

In the above scheme, the compound of general formula (3) may be reacted with tetra-n-butyl ammonium fluoride to give a compound of general formula (4) (step 3). Suitable solvents for use in the above step 3 include N, N- dimethylformamide, dimethylsulfoxide, N,N-dimethylacetamide, 1 ,3-dimethyl- 2-imidazolidinone, tetrahydrofuran, toluene, acetonitrile, more preferably tetrahydrofuran. The reaction temperature of the above step 3 is in the range from 0 °C to 100 °C, preferably from 0 °C to 50 0C, though it is not specifically limited so far as the reaction proceeds.

R R R5 step 4

In the above scheme, the compound of general formula (4) may be reacted with a ketone or an aldehyde, described as R12(C=O)RI 3, in the presence of a base to give a compound of general formula (5) (step 4). Suitable bases for use in the above step 4 include n-butyl lithium, sec- butyl lithium, tert-butyl lithium, methyl lithium, phenyl lithium, methyl magnesium bromide, methyl magnesium chloride, methyl magnesium iodide, isopropyl magnesium bromide, diisopropyl magnesium, lithium diisopropylamide, lithium bis(trimethylsilyl)amide, lithium 2,2,6,6- tetramethylpiperidide, lithium amide, sodium hydride, sodium bis(trimethylsilyl)amide, potassium hydride, potassium bis(trimethylsilyl) more preferably n-butyl lithium. Suitable solvents for use in the above step 4 include hydrocarbon- ether-based solvents or the likes, such as pentane, hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, anisole, more preferably tetrahydrofuran. The reaction temperature of the above step 1 is in the range from - 100 °C to 50 0C, preferably from -80 °C to 30 0C, though it is not specifically limited so far as the reaction proceeds.

R R5 R5 step 5

In the above scheme, the compound of general formula (5) may be reduced to give a compound of general formula (6) (step 5). Step 5 includes the reduction by LJAIH4, Red-AI (sodium bis(2- methoxyethoxy)aluminium hydride) or hydrogenation using Lindlar catalyst. Suitable solvents for use in the reduction by lithium aluminum hydride or Red-AI include hydrocarbon- ether-based solvents or the like, such as pentane, hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2-dimethoxyethane, 1,4-dioxane, anisole, more preferably tetrahydrofuran. Suitable solvents for use in the hydrogenation by Lindlar catalyst include methanol, ethanol, ethyl acetate, more preferably methanol. The reaction temperature of the above step 5 is in the range from -50 °C to 200 °C, preferably from 0 °C to 100 °C, though it is not specifically limited so far as the reaction proceeds. RIv^ ^R R5 step 6

Ri3

In the above scheme, the compound of general formula (5, 6) may be subjected to hydrogenation to give a compound of general formula (7) (step 6). Suitable catalysts for use in the above step 6 include palladium-, rhodium-, ruthenium-, nickel-, platinum-based catalysts or the like, such as palladium on carbon, palladium hydroxide, platinum oxide, rhodium on alumina, Wilkinson's catalyst, more preferably palladium on carbon. Suitable solvents for use in the above step 6 include methanol, ethanol, ethyl acetate, acetic acid, more preferably methanol. The reaction temperature of the above step 6 is in the range from -50 0C to 200 °C, preferably from 0 °C to 100 °C, though it is not specifically limited so far as the reaction proceeds. R5 ~^OR' R4 R6 K13

R5

In the above scheme, the compound of general formula (5-7) may be subjected to protection of hydroxyl group with a compound of general formula (9) (R' = a methoxymethyl group, a 2-(trimethylsilyl)ethoxymethyl group, a benzyl group, a p-methoxybenzyl group, a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a t-buthyldiphenylsilyl group or an acetyl group; X = a halogen atom, a methanesulfonyloxy group, a toluenesulfonyloxy group, a trifluoromethanesulfonyloxy group or an acethyloxy group) in the presence of a base to give a compound of general formula (8) (step 7). Suitable bases for use in the above step 7 include sodium tert- butoxide, potassium tert-butoxide, n-butyl lithium, sec-butyl lithium, tert-butyl lithium, lithium diisopropylamide, lithium dicyclohexylamide, lithium bis(trimethylsilyl)amide, potassium bis(trimethylsilyl)amide, sodium hydride, potassium hydride, potassium carbonate, sodium carbonate, sodium hydrogencarbonate, cesium carbonate, pyridine, triethylamine, diisopropylethylamine, 2,6-lutidine, 2,4,6-collidine, N1N- dimethylaminopyridine, more preferably sodium hydride, potassium carbonate, or pyridine. Suitable solvents for use in the above step 7 include dichloromethane, 1 ,2-dichloroethane, chloroform, hexane, benzene, toluene, diethyl ether, t- butyl methyl ether, tetrahydr ;ran, 1 ,2-dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, N,N-dimethylformamide, dimethylsulfoxide, N1N- dimethylacetamide.i .S-dimethyl^-imidazolidinone.i .S-dimethyl-S^.δ.e- tetrahydro-2(1 H)-pyrimidinone, acetonitrile, more preferably N1N- dimethylformamide. The reaction temperature of the above step 7 is in the range from -50 °C to 200 °C, preferably from -20 °C to 100 °C, though it is not specifically limited so far as the reaction proceeds. R R. R5 R5 step 8

R4 R6 ' T R R ■12 ■13 ■13 5,6,7,8 ^h/ >n 10 In the above scheme, the compound of general formula (5-8) (R = a hydrogen atom, a methoxymethyl group, a 2-(trimethylsilyl)ethoxymethyl group, a benzyl group, a p-methoxybenzyl group, a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a t-buthyldiphenylsilyl group or an acetyl group) may be subjected to alkylation with a compound of general formula (10) (m = an integer of 1 to 5, n = an integer of 1 to 5, X = a halogen atom, a methanesulfonyloxy group, a toluenesulfonyloxy group or a trifluoromethanesulfonyloxy group) in the presence of a base to give a compound of general formula (11) (step 8). Suitable bases for use in the above step 8 include sodium methoxide, sodium ethoxide, sodium tert-butoxide, potassium methoxide, potassium ethoxide, potassium tert-butoxide, n-butyl lithium, sec-butyl lithium, tert-butyl lithium, lithium diisopropylamide, lithium dicyclohexylamide, lithium bis(trimethylsilyl)amide, potassium bis(trimethylsilyl)amide, sodium hydride, potassium hydride, potassium carbonate, sodium carbonate, sodium hydrogencarbonate, cesium carbonate, more preferably sodium hydride or potassium carbonate. Suitable solvents for use in the above step 8 include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, N.N-dimethylformamide, dimethylsulfoxide, N,N-dimethylacetamide, 1 ,3-dimethyl-2-imidazolidinone, 1 ,3-dimethyl-3,4,5,6-tetrahydro-2(1 H)-pyrimidinone, methanol, ethanol, isopropanol, acetonitrile, more preferably N,N-dimethylformamide. The reaction temperature of the above step 8 is in the range from -50 0C to 200 °C, preferably from 0 °C to 100 0C, though it is not specifically limited so far as the reaction proceeds. In addition, the compound of general formula (5-8) may be subjected to alkylation with a compound of general formula (10) (X = a hydroxyl group) in the presence of triphenylphosphine and dialkyl azocarboxylate to give a compound of general formula (11) in the above scheme (step 8). In the case using a compound of general formula (10) (X = a hydroxyl group), suitable solvents for use in the above step 8 include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, dichloromethane, 1 ,2- dichloroethane, chloroform, more preferably toluene, tetrahydrofuran. In the case using a compound of general formula (10) (X = a hydroxyl group), the reaction temperature of the above step 8 is in the range from -50 °C to 200 °C, preferably from -20 0C to 50 °C, though it is not specifically limited so far as the reaction proceeds. Compound 11 can also be synthesized from compound 4 in order of step 8, step 4, step 5, step 6 and step 7. R3\/Ϊ^>\/^'R5 R3 - ^ 0 0XJ UW^OR H0 0. ^cA R4 ∏ Rβ Ri3 '2 HO^n In the above scheme, the compound of general formula (11) may be subjected to deprotection in the presence of an acid to give a compound of general formula (12) (step 9). Suitable acids for use in the above step 9 include hydrochloric acid, sulfuric acid, acetic acid, phosphoric acid, trifluoroacetic acid, 10- camphorsulfonic acid, p-toluenesulfonic acid, pyridinium p-toluenesuifonic acid, trifluoroborane-diethyl ether complex, carbon tetrabromide, trimethylsilyl bromide, methanesulfonic acid, acidic ion exchange resin. Suitable solvents for use in the above step 9 include dichloromethane, 1 ,2-dichloroethane, chloroform, acetone, methanol, ethanol, tetrahydrofuran, 1 ,2-dimethoxyethane, 1 ,4-dioxane, diethyl ether, water, the mixtures. The reaction temperature of the above step 9 is in the range from -10 0C to 150 °C, preferably from 0 0C to 100 °C, though it is not specifically limited so far as the reaction proceeds.

R1 R5 Rs step 10 OR o^o

13 In the above scheme, the compound of general formula (5-8) may be subjected to alkylation with a compound of general formula (13) (m = an integer of 1 to 5, X = a halogen atom, a methanesulfonyloxy group, a toluenesulfonyloxy group or a trifluoromethanesulfonyloxy group) in the presence of a base to give a compound of general formula (14) (step 10). Suitable bases for use in the above step 10 include sodium tert- butoxide, potassium tert-butoxide, n-butyl lithium, sec-butyl lithium, tert-butyl lithium, lithium diisopropylamide, lithium dicyclohexylamide, lithium bis(trimethylsilyl)amide, potassium bis(trimethylsilyl)amide, sodium hydride, potassium hydride, potassium carbonate, sodium carbonate, sodium hydrogencarbonate, cesium carbonate, more preferably potassium carbonate. Suitable solvents for use in the above step 10 include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, N,N-dimethylformamide, dimethylsulfoxide, N.N-dimethylacetamide, 1 ,3-dimethyl-2-imidazolidinone, 1 ,3-dimethyl-3,4,5,6-tetrahydro-2(1 H)-pyrimidinone, methanol, ethanol, isopropanol, acetonitrile, more preferably N,N-dimethylformamide. The reaction temperature of the above step 10 is in the range from - 50 0C to 200 °C, preferably from 0 °C to 150 0C, though it is not specifically limited so far as the reaction proceeds. In addition, the compound of general formula (5-8) may be subjected to alkylation with a compound of general formula (13) (X = a hydroxyl group) in the presence of triphenylphosphine and dialkyl azocarboxylate to give a compound of general formula (14) in the above scheme (step 10). In the case using a compound of general formula (13) (X = a hydroxyl group), suitable solvents for use in the above step 10 include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, dichloromethane, 1 ,2- dichloroethane, chloroform, more preferably toluene, tetrahydrofuran. In the case using a compound of general formula (13) (X = a hydroxyl group), the reaction temperature of the above step 10 is in the range from - 50 °C to 200 °C, preferably from -20 0C to 50 °C, though it is not specifically limited so far as the reaction proceeds.

| T I T step 11 f { η^o-Kf -γ°R . Hooc ° R4 14 Re Ria 12 In the above scheme, the compound of general formula (14) may be hydrolyzed in the presence of a base to give a compound of general formula (15) (step 11). Suitable bases for use in the above step 11 include sodium hydroxide, potassium hydroxide, lithium hydroxide, potassium carbonate, sodium carbonate, sodium hydrogencarbonate, cesium carbonate, more preferably sodium hydroxide or potassium hydroxide. Suitable solvents for use in the above step 11 include acetone, methanol, ethanol, tetrahydrofuran, 1 ,4-dioxane, 1 ,2-dimethoxyethane, water, the mixtures more preferably methanol-water mixture. The reaction temperature of the above step 11 is in the range from - 10 °C to 120 °C, preferably from 0 °C to 100 °C, though it is not specifically limited so far as the reaction proceeds.

R5

R4 5,6,7,8

In the above scheme, the compound of general formula (5-8) may be subjected to alkylation with a compound of general formula (16) (p = an integer of 1 to 10, X = a halogen atom, a methanesulfonyloxy group, a toluenesulfonyloxy group or a trifluoromethanesulfonyloxy group) in the presence of a base to give a compound of general formula (17) (step 12). Suitable bases for use in the above step 12 include sodium tert- butoxide, potassium tert-butoxide, n-butyl lithium, sec-butyl lithium, tert-butyl lithium, lithium diisopropylamide, lithium dicyclohexylamide, lithium bis(trimethylsilyl)amide, potassium bis(trimethylsilyl)amide, sodium hydride, potassium hydride, potassium carbonate, sodium carbonate, sodium hydrogencarbonate, cesium carbonate, more preferably potassium carbonate. Suitable solvents for use in the above step 12 include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, N,N-dimethylformamide, dimethylsulfoxide, N,N-dimethylacetamide, 1 ,3-dimethyl-2-imidazolidinone, 1 ,3-dimethyl-3,4,5,6-tetrahydro-2(1 H)-pyrimidinone, methanol, ethanol, isopropanol, acetonitrile, more preferably N,N-dimethylformamide. The reaction temperature of the above step 12 is in the range from - 50 0C to 200 °C, preferably from 0 °C to 100 °C, though it is not specifically limited so far as the reaction proceeds. In addition, the compound of general formula (5-8) may be subjected to alkylation with a compound of general formula (16) (X = a hydroxyl group) in the presence of triphenylphosphine and dialkyl azocarboxylate to give a compound of general formula (17) in the above scheme (step 12). In the case using a compound of general formula (16) (X = a hydroxyl group), suitable solvents for use in the above step 12 include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, dichloromethane, 1 ,2- dichloroethane, chloroform, more preferably toluene, tetrahydrofuran. In the case using a compound of general formula (16) (X = a hydroxyl group), the reaction temperature of the above step 12 is in the range from - 50 °C to 200 °C, preferably from -20 °C to 50 °C, though it is not specifically limited so far as the reaction proceeds.

R1. .R5

In the above scheme, the compound of general formula (17) may be hydrolyzed in the presence of a base to give a compound of general formula (18) (step 13). Suitable bases for use in the above step 13 include sodium hydroxide, potassium hydroxide, lithium hydroxide, potassium carbonate, sodium carbonate, sodium hydrogencarbonate, cesium carbonate, more preferably sodium hydroxide or potassium hydroxide. Suitable solvents for use in the above step 13 include acetone, methanol, ethanol, propanol, isopropanol, tetrahydrofuran, 1 ,4-dioxane, 1,2- dimethoxyethane, water, the mixtures more preferably methanol-water mixture. The reaction temperature of the above step 13 is in the range from - 10 °C to 120 °C, preferably from 0 °C to 100 °C, though it is not specifically limited so far as the reaction proceeds. R5

o \_ 19 In the above scheme, the compound of general formula (5-8) may be subjected to alkylation with a compound of general formula (19) (q = an integer of 2 to 10, X = a halogen atom, a methanesulfonyloxy group, a toluenesulfonyloxy group or a trifluoromethanesulfonyloxy group) in the presence of a base to give a compound of general formula (20) (step 14). Suitable bases for use in the above step 14 include sodium tert- butoxide, potassium tert-butoxide, n-butyl lithium, sec-butyl lithium, tert-butyl lithium, lithium diisopropylamide, lithium dicyclohexylamide, lithium bis(trimethylsilyl)amide, potassium bis(trimethylsilyl)amide, sodium hydride, potassium hydride, potassium carbonate, sodium carbonate, sodium hydrogencarbonate, cesium carbonate, more preferably potassium carbonate. Suitable solvents for use in the above step 14 include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, N,N-dimethylformamide, dimethylsulfoxide, N,N-dimethylacetamide, 1 ,3-dimethyl-2-imidazolidinone, 1 ,3-dimethyl-3,4,5,6-tetrahydro-2(1 H)-pyrimidinone, methanol, ethanol, isopropanol, acetonitrile, more preferably acetonitrile. The reaction temperature of the above step 14 is in the range from - 50 °C to 200 °C, preferably from 0 °C to 100 0C, though it is not specifically limited so far as the reaction proceeds. In addition, the compound of general formula (5-8) may be subjected to alkylation with a compound of general formula (19) (X = a hydroxyl group) in the presence of triphenylphosphine and dialkyl azocarboxylate to give a compound of general formula (20) in the above scheme (step 14). In the case using a compound of general formula (19) (X = a hydroxyl group), suitable solvents for use in the above step 14 include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, dichloromethane, 1 ,2- dichloroethane, chloroform, more preferably toluene, tetrahydrofuran. In the case using a compound of general formula (19) (X = a hydroxyl group), the reaction temperature of the above step 14 is in the range from - 50 °C to 200 °C, preferably from -20 °C to 50 °C, though it is not specifically limited so far as the reaction proceeds.

R. step 15 "O" ^T y ^'^ .O~R" „ H2M* T-Q. OR .„ .. RR RM R4 , O 20 21 In the above scheme, the step for obtaining a compound of general formula (21) from the compound of general formula (20) may be performed with hydrazine or methylamine (step 15). Suitable solvents for use in the above step 15 include methanol, ethanol, n-propanol, isopropanol, more preferably methanol. The reaction temperature of the above step 15 is in the range from 0 °C to 200 0C, preferably from 0 °C to 100 °C, though it is not specifically limited so far as the reaction proceeds.

R R Rβv step 16 TfO RR 21 22 In the above scheme, the compound of general formula (21 ) (R20 = an optionally protected hydroxyl group, an optionally substituted C1-15 alkyl group or an optionally substituted C1-8 alkoxyl group) may be reacted with allyltributyltin in the presence of a palladium catalyst and lithium chloride to give a compound of general formula (22) (step 16). Suitable palladium catalysts for use in the above step 16 include tetrakis(triphenylphosphine)palladium, Pd(dba)2, Pd2(dba)3-CHCI3, palladium acetate, palladium chloride, [1 ,1'-bis(diphenylphosphino)- ferrocene]palladium dichloride dichloromethane complex, (dba; dibenzylideneacetone) A ligand, such as triphenylphosphine, tributhylphosphine, tricyclohexylphosphine, 1 ,3-bis(diphenylphosphinopropane) or tri-t-buthyl phosphine, may be used in the above step 16 to increase the activity of catalyst or the reaction selectivity. Suitable solvents for use in the above step 16 include N1N- dimethylformamide, dimethylsulfoxide, N,N-dimethylacetamide, 1 ,-dimethyl- 2-imidazolidinone, tetrahydrofuran, toluene, acetonitrile, more preferably N,N-dimethylformamide. The reaction temperature of the above step 16 is in the range from 0 °C to 200 °C, preferably from 20 0C to 150 °C, though it is not specifically limited so far as the reaction proceeds. Ri\/R2 step 17 R3

R6 22 In the above scheme, the compound of general formula (22) (R20 = an optionally protected hydroxyl group, an optionally substituted C1-15 alkyl group or an optionally substituted C1-8 alkoxyl group) may be subjected to hydroboration and oxidation to give a compound of general formula (23) (step 17). Suitable hydroboration reagents for use in the above step 17 include borane-tetrahydrofuran complex, borane-methyl sulfide complex, borane- pyridine complex, borane-trimethylamine complex, or 9-BBN. Suitable oxidizing agents for use in the above step 17 include hydrogen peroxide-sodium hydroxide, or sodium perborate. Suitable solvent for use in the above step 17 includes tetrahydrofuran. The reaction temperature of the above step 17 is in the range from - 78 °C to 100 0C, preferably from -50 °C to 50 °C, though it is not specifically limited so far as the reaction proceeds. Ri R3 step 18 R OHC R6 R6 23 24 In the above scheme, the compound of general formula (23) (R20 = an optionally protected hydroxyl group, an optionally substituted C1-15 alkyl group or an optionally substituted C1-8 alkoxyl group) may be oxidized to give a compound of general formula (24) (step 18). Suitable oxidizing agents for use in the above step 18 include pyridinium chlorochromate, pyridinium dichromate, manganese dioxide, osmium tetraoxide, ruthenium trichloride, tetrapropylammonium perruthenate, oxaryl chloride/dimethyl sulfoxide/triethylamine, triphosgene/dimethyl sulfoxide, sulfur trioxide pyridine complex/dimethyl sulfoxide, acetone/aluminium triisopropoxide, cyclohexanone/aluminium triisopropoxide, Dess-Martin reagent, more preferably Dess-Martin reagent Suitable solvents for use in the above step 18 include benzene, toluene, hexane, heptane, dichloromethane, 1 ,2-dichloroethane, chloroform, tetrahydrofuran, acetone, water, more preferably dichloromethane. The reaction temperature of the above step 18 is in the range from - 78 °C to 50 °C, preferably from 0 °C to 50 °C, though it is not specifically limited so far as the reaction proceeds.

R1 R1* R3^ step 19 R3 OHC R6 24 25 In the above scheme, the compound of general formula (24) (R20 = an optionally protected hydroxyl group, an optionally substituted C1-15 alkyl group or an optionally substituted C1-8 alkoxyl group) may be subjected to alkylation with Wittig reagent, such as R21CH2-PPh3G (R21 = a hydrogen atom or an optionally substituted C1-15 alkyl group; G = a halogen atom) in the presence of a base to give a compound of general formula (25) (step 19). Suitable Wittig reagents for use in the above step 19 include methyl triphenylphosphonium bromide, ethyl triphenylphosphonium bromide, n- propyl triphenylphosphonium iodide, isopropyl triphenylphosphonium iodide etc. Suitable bases for use in the above step 19 include sodium methoxide, sodium ethoxide, sodium tert-butoxide, potassium tert-butoxide, n-butyl lithium, sec-butyl lithium, tert-butyl lithium, lithium diisopropylamide, lithium dicyclohexylamide, lithium bis(trimethylsilyl)amide, potassium bis(trimethylsilyl)amide, sodium hydride, potassium hydride, more preferably n-butyl lithium. Suitable solvents for use in the above step 19 include diethyl ether, tetrahydrofuran, benzene, toluene, dimethylsulfoxide, more preferably tetrahydrofuran. The reaction temperature of the above step 19 is in the range from - 78 °C to 120 0C, preferably from -78 °C to 50 °C, though it is not specifically limited so far as the reaction proceeds.

R1 R3

25 26 In the above scheme, the compound of general formula (25) (R20 = an optionally protected hydroxyl group, an optionally substituted C1-15 alkyl group or an optionally substituted C1-8 alkoxyl group; R21 = a hydrogen atom or an optionally substituted C1-15 alkyl group) may be reacted with osmium tetraoxide/4-methylmorpholine N-oxide to give a compound of general formula (26) (step 20). Suitable solvents for use in the above step 20 include acetone, acetonitrile, t-butanol, water or mixtures, more preferably acetone/t- butanol/water mixture. The reaction temperature of the above step 20 is in the range from - 78 °C to 120 °C, preferably from -40 0C to 50 °C, though it is not specifically limited so far as the reaction proceeds.

NC R4 2s R, 27 In the above scheme, the compound of general formula (5-8) may be subjected to alkylation with a compound of general formula (27) (s = an integer of 1 to 10, X = a halogen atom, a methanesulfonyloxy group, a toluenesulfonyloxy group or a trifluoromethanesulfonyloxy group) in the presence of a base to give a compound of general formula (28) (step 21 ). Suitable bases for use in the above step 21 include sodium tert-butoxide, potassium tert-butoxide, n-butyl lithium, sec-butyl lithium, tert-butyl lithium, lithium diisopropylamide, lithium dicyclohexylamide, lithium bis(trimethylsilyl)amide, potassium bis(trimethylsilyl)amide, sodium hydride, potassium hydride, potassium carbonate, sodium carbonate, sodium hydrogencarbonate, cesium carbonate, more preferably potassium carbonate. Suitable solvents for use in the above step 21 include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, N,N-dimethylformamide, dimethylsulfoxide, N,N-dimethylacetamide, 1 ,3-dimethyl-2-imidazolidinone, 1 ,3-dimethyl-3,4,5,6-tetrahydro-2(1 H)-pyrimidinone, methanol, ethanol, isopropanol, acetonitrile, more preferably acetonitrile. The reaction temperature of the above step 21 is in the range from - 50 °C to 200 °C, preferably from 0 0C to 100 °C, though it is not specifically limited so far as the reaction proceeds. R. R5 R5 step 22 NCΓ *Ό OR OR N-NH

In the above scheme, the step for obtaining a compound of general formula (29) from the compound of general formula (28) may be performed with sodium azide, combination of sodium azide and triethyamine hydrochloride salt, azidotributyltin or combination of trimethylsilylazide and di-n-butyltinoxide (step 22). Suitable solvents for use in the above step 22 include benzene, toluene, xylene, dyglyme. The reaction temperature of the above step 22 is in the range from 0 0C to 200 0C, preferably from 10 °C to 150 °C, though it is not specifically limited so far as the reaction proceeds.

R5 Rfi step 23

R4 R6 ^'Y R-13°* — - 5,6,7,8 In the above scheme, the compound of general formula (5-8) may be reacted with trifluoromethanesulfonic acid anhydride in the presence of a base to give a compound of general formula (30) (step 23). Suitable bases for use in the above step 23 include pyridine, 2,6- lutidine, 2,4,6-collidine,N,N-dimethylaminopyridine, imidazole, triethylamine, more preferably pyridine. Suitable solvents for use in the above step 23 include diethyl ether, tetrahydrofuran, dichloromethane, 1,2-dichloroethane, chloroform, benzene, toluene, more preferably dichloromethane. The reaction temperature of the above step 23 is in the range from - 50 °C to 50 °C, preferably from -20 0C to 30 °C, though it is not specifically limited so far as the reaction proceeds. R3S R5 R3 R5 step 24 Tfcr ^ ^r ^'xz: R22OOC OR R4 R6 30 ' '" 31 In the above scheme, the compound of general formula (30) may be reacted with acrylic acid ester in the presence of a palladium catalyst, and triethyamine to give a compound of general formula (31) (R22 = a C1-3 alkyl group)(step 24). Suitable palladium catalysts for use in the above step 24 include tetrakis(triphenylphosphine)palladium, Pd(dba)2, Pd2(dba)3-CHCI3, palladium acetate, palladium chloride, [1 ,1'-bis(diphenylphosphino)- ferrocene]palladium dichloride dichloromethane complex, (dba; dibenzylideneacetone) A ligand, such as triphenylphosphine, tributhylphosphine, tricyclohexylphosphine, 1 ,3-bis(diphenylphosphinopropane) or tri-t-buthyl phosphine, may be used in the above step 24 to increase the catalytic activity and/or the reaction selectivity. Suitable solvents for use in the above step 24 include N, N- dimethylformamide, dimethylsulfoxide, N.N-dimethylacetamide, 1 ,3-dimethyl- 2-imidazolidinone, tetrahydrofuran, toluene, acetonitrile, more preferably N,N-dimethylformamide or acetonitrile. The reaction temperature of the above step 24 is in the range from 0 °C to 200 °C, preferably from 20 °C to 150 °C, though it is not specifically limited so far as the reaction proceeds. R3 step 25 OR R22OOC R22OOC R4 31 - - 32 R6 R13 In the above scheme, the compound of general formula (31 ) (R22 = a C1-3 alkyl group) may be reacted with NaBH4 in the presence of NiCI2- 6H2O to give a compound of general formula (32) (R22 = a C1-3 alkyl group) (step 25). Suitable solvents for use in the above step 25 include methanol, ethanol, isopropanol, dichloromethane, 1 ,2-dichloroethane or mixtures, more preferably methanol/dichloromethane mixture. The reaction temperature of the above step 25 is in the range from - 40 0C to 100 °C, preferably from -20 °C to 50 0C, though it is not specifically limited so far as the reaction proceeds.

R R3^ R5 R3 step 26 OR R22OOC HOOC R6 13 R6 "M3 32 33 In the above scheme, the compound of general formula (32) (R22 = a C1-3 alkyl group) may be hydrolyzed in the presence of a base to give a compound of general formula (33) (step 26). Suitable bases for use in the above step 26 include sodium hydroxide, potassium hydroxide, lithium hydroxide, potassium carbonate, sodium carbonate, sodium hydrogencarbonate, cesium carbonate, tetrabutylammonium fluoride, more preferably sodium hydroxide, potassium hydroxide or tetrabutylammonium fluoride. Suitable solvents for use in the above step 26 include acetone, methanol, ethanol, tetrahydrofuran, 1 ,4-dioxane, 1 ,2-dimethoxyethane, water, the mixtures more preferably methanol-water mixture or tetrahydrofuran. The reaction temperature of the above step 26 is in the range from - 10 °C to 120 °C, preferably from 0 °C to 100 0C, though it is not specifically limited so far as the reaction proceeds.

R1 R5 R3 R* step 27 OR OR R22OOC. R4 R6 " 30 " 34 In the above scheme, the compound of general formula (30) may be reacted with acetylene derivative in the presence of a palladium catalyst, copper (I) iodide, and triethyamine to give a compound of general formula (34) (R22 = a C1-3 alkyl group)(step 27). Suitable palladium catalysts for use in the above step 27 include PdCI2(dppf)2-CH2CI2 complex, tetrakis(triphenylphosphine)palladium, Pd(dba)2, Pd2(dba)3-CHCI3, palladium acetate, palladium chloride, (dba; dibenzylideneacetone, dppf; diphenylphosphino)ferrocene) A ligand, such as triphenylphosphine, tributhylphosphine, tricyclohexylphosphine, 1 ,3-bis(diphenylphosphinopropane) or tri-t-buthyl phosphine, may be used in the above step 27 to increase the catalytic activity and/or the reaction selectivity. Suitable solvents for use in the above step 27 include N, N- dimethylformamide, dimethylsulfoxide, N.N-dimethylacetamide, 1 ,3-dimethyl- 2-imidazolidinone, tetrahydrofuran, toluene, acetonitrile, more preferably N,N-dimethylformamide or acetonitrile. The reaction temperature of the above step 27 is in the range from 0 °C to 200 °C, preferably from 20 °C to 150 °C, though it is not specifically limited so far as the reaction proceeds. The compound of general formula (34) (R22 = a C1-3 alkyl group) may be hydrolyzed by the same procedure as described in step 26 to give the corresponding carboxylic acid.

R R3 R5 step 28 OR .OR R4 R6 5,6,7,8 O^NH 35 In the above scheme, the compound of general formula (5-8) may be subjected to alkylation with a compound of general formula (35) (m = an integer of 1 to 5, X = a halogen atom, a methanesulfonyloxy group, a toluenesulfonyloxy group or a trifluoromethanesulfonyloxy group) in the presence of a base to give a compound of general formula (36) (step 28). Suitable bases for use in the above step 28 include sodium tert- butoxide, potassium tert-butoxide, n-butyl lithium, sec-butyl lithium, tert-butyl lithium, lithium diisopropylamide, lithium dicyclohexylamide, lithium bis(trimethylsilyl)amide, potassium bis(trimethylsilyl)amide, sodium hydride, potassium hydride, potassium carbonate, sodium carbonate, sodium hydrogencarbonate, cesium carbonate, more preferably potassium carbonate. Suitable solvents for use in the above step 28 include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, N,N-dimethylformamide, dimethylsulfoxide, N.N-dimethylacetamide, 1 ,3-dimethyl-2-imidazolidinone, 1 ,3-dimethyl-3,4,5,6-tetrahydro-2(1 H)-pyrimidinone, methanol, ethanol, isopropanol, acetonitrile, more preferably N,N-dimethylformamide, acetonitrile. The reaction temperature of the above step 28 is in the range from - 50 0C to 200 °C, preferably from 0 0C to 100 °C, though it is not specifically limited so far as the reaction proceeds. In addition, the compound of general formula (5-8) may be subjected to alkylation with a compound of general formula (35) (X = a hydroxyl group) in the presence of triphenylphosphine and dialkyl azocarboxylate to give a compound of general formula (36) in the above scheme (step 28). In the case using a compound of general formula (35) (X = a hydroxyl group), suitable solvents for use in the above step 28 include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, dichloromethane, 1 ,2- dichloroethane, chloroform, more preferably toluene, tetrahydrofuran. In the case using a compound of general formula (35) (X = a hydroxyl group), the reaction temperature of the above step 28 is in the range from - 50 °C to 200 0C, preferably from -20 °C to 50 °C, though it is not specifically limited so far as the reaction proceeds. R3 R5 step 29 OR HOOC O^NH R4 NH

In the above scheme, the compound of general formula (36) may be hydrolyzed in the presence of an acid to give a compound of general formula (37) (step 29). Suitable acids for use in the above step 29 include hydrochloric acid, hydrobromic acid, sulfuric acid, acetic acid, phosphoric acid, trifluoroacetic acid, 10-camphorsulfonic acid, p-toluenesulfonic acid, methanesulfonic acid, more preferably hydrochloric acid. Suitable solvents for use in the above step 29 include acetone, methanol, ethanol, tetrahydrofuran, 1 ,2-dimethoxyethane, 1 ,4-dioxane, diethyl ether, water, the mixtures. The reaction temperature of the above step 29 is in the range from 0 °C to 200 °C, preferably from 20 °C to 120 0C, though it is not specifically limited so far as the reaction proceeds.

R5 R3 R5 step 30 H0Ηγ^0- R6 12 tR12 0A

In the above scheme, the compound of general formula (12) may be subjected to cyclization in the presence of triphenylphosphine and dialkyl azocarboxylate to give a compound of general formula (38) (step 30). Suitable solvents for use in the above step 30 include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, dichloromethane, 1 ,2- dichloroethane, chloroform, more preferably toluene, tetrahydrofuran. The reaction temperature of the above step 30 is in the range from - 50 °C to 200 0C, preferably from -20 0C to 50 °C, though it is not specifically limited so far as the reaction proceeds. Rw ^Ro Rs ^γOR ^γOR D R6 K-13 K12 R4 R6 R K-i3 12 18 39

In the above scheme, the compound of general formula (18) may be reacted with amine derivative NHR23(R24) (R23 = a hydrogen atom or a C1-3 alkyl group, R24 is represented by following formula) in the presence of coupling reagent used to form amide bonds, after that, may be subjected to deprotection to give a compound of general formula (39) (step 31). R24: Ra Rb COORc v ;n Ra and Rb are each independently selected from the group consisiting of a hydrogen atom, an optionally substituted C1-10 alkyl group, an optionally substituted C3-10 cycloalkyl group, an optionally substituted phenyl group, an optionally substituted benzyl group, an optionally substituted phenethyl group, or Ra and Rb may together form an optionally substituted C3-10 cycloalkyl group. The substitution group is a hydroxyl group, an amino group, a carboxyl group or a carboxylic amide group with an appropriate protecting group described in Protecting Groups in Organic Synthesis, third edition, John Wiley & Sons, Inc., for example, tert-butyl group, tert-butoxycarbonyl group, trityl group. Rc is a protecting group selected from a C1-5 alkyl group or polystylene-bound 4-benzyloxy-benzyl group. In the deprotection step, the cleavage of a protecting group such as tert-butyl group, tert-butoxycarbonyl group, trityl group or polystylene-bound 4-benzyloxy-benzyl group may be carried by trifluoroacetic acid in dichloromethane. Suitable coupling reagents for use in the above step 31 include 1 ,3- dicylcohexylcarbodiimide, 1 ,3-diisopropylcarbodiimide, N-ethyl-N'-(3- dimethylaminopropyl)carbodiimide, benzotriazol-1-yloxy- tris(dimethylamino)phosphonium hexafluorophosphate, diphenylphosphoryl azide. In the coupling step, a reagent, such as N-hydroxysuccinimide, 1- hydroxybenzotriazole or hydroxy-3,4-dihydro-4-oxo-1 ,2,3-benzotriazine may be used in the above step 31 to increase the yields. Suitable solvents for use in the coupling process in step 31 include benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, dichloromethane, 1 ,2- dichloroethane, chloroform, N,N-dimethylformamide, dimethylsulfoxide, N, N- dimethylacetamide, 1 ,3-dimethyl-2-imidazolidinone, 1 ,3-dimethyl-3,4,5,6- tetrahydro-2(1 H)-pyrimidinone, acetonitrile. The reaction temperature of the above step 31 is in the range from - 50 °C to 200 °C, preferably from -20 °C to 50 °C, though it is not specifically limited so far as the reaction proceeds.

step 32 OTf HO R4 OTBS In the above scheme, the compound of general formula (2) may be reacted with tert-butyl-(1-tert-butyl-prop-2-ynyloxy)-dimethyl-silane in the presence of a palladium catalyst, copper (I) iodide, and triethyamine to give a compound of general formula (40) (step 32). Suitable palladium catalysts for use in the above step 32 include tetrakis(triphenylphosphine)palladium, Pd(dba)2, Pd2(dba)3-CHCI3, palladium acetate, palladium chloride, [1 ,1'-bis(diphenylphosphino)- ferrocene]palladium dichloride dichloromethane complex, (dba; dibenzylideneacetone) A ligand, such as triphenylphosphine, tributhylphosphine, tricyclohexylphosphine, 1 ,3-bis(diphenylphosphinopropane) or tri-t-buthyl phosphine, may be used in the above step 32 to increase the catalytic activity and/or the reaction selectivity. Suitable solvents for use in the above step 32 include N, N- dimethylformamide, dimethylsulfoxide, N,N-dimethylacetamide, 1 ,3-dimethyl- 2-imidazolidinone, tetrahydrofuran, toluene, acetonitrile, more preferably N.N-dimethylformamide or acetonitrile. The reaction temperature of the above step 32 is in the range from 0 °C to 200 0C, preferably from 20 °C to 150 °C, though it is not specifically limited so far as the reaction proceeds.

R3 .R= < HO J^o R4 R6 Ri3 lz " ((^ u 51COOR25 5,6,7,8

41 In the above scheme, the compound of general formula (5-8) may be subjected to alkylation with a compound of general formula (41) (m' = 0 or 1 , n' = 0, 1 or 2, A = an oxygen atom, a sulfur atom, a nitrogen atom or a carbon atom, X = a halogen atom, a methanesulfonyloxy group, a toluenesulfonyloxy group or a trifluoromethanesulfonyloxy group, R25 = a C1-4 alkyl group) in the presence of a base to give a compound of general formula (42) (step 33). Suitable bases for use in the above step 33 include sodium tert- butoxide, potassium tert-butoxide, n-butyl lithium, sec-butyl lithium, tert-butyl lithium, lithium diisopropylamide, lithium dicyclohexylamide, lithium bis(trimethylsilyl)amide, potassium bis(trimethylsilyl)amide, sodium hydride, potassium hydride, potassium carbonate, sodium carbonate, sodium hydrogencarbonate, cesium carbonate, more preferably potassium carbonate. Suitable solvents for use in the above step 33 include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, N,N-dimethylformamide, dimethylsulfoxide, N,N-dimethylacetamide, 1 ,3-dimethyl-2-imidazolidinone, 1 ,3-dimethyl-3,4,5,6-tetrahydro-2(1 H)-pyrimidinone, methanol, ethanol, isopropanol, acetonitrile,, acetone more preferably N,N-dimethylformamide, acetone. The reaction temperature of the above step 33 is in the range from - 50 °C to 200 °C, preferably from 0 °C to 100 °C, though it is not specifically limited so far as the reaction proceeds. In addition, the compound of general formula (5-8) may be subjected to alkylation with a compound of general formula (41 ) (X = a hydroxyl group) in the presence of triphenylphosphine and dialkyl azocarboxylate to give a compound of general formula (42) in the above scheme (step 33). In the case using a compound of general formula (41) (X = a hydroxyl group), suitable solvents for use in the above step 33 include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, dichloromethane, 1 ,2- dichloroethane, chloroform, more preferably toluene, tetrahydrofuran. In the case using a compound of general formula (41) (X = a hydroxyl group), the reaction temperature of the above step 33 is in the range from - 50 °C to 200 °C, preferably from -20 °C to 50 °C, though it is not specifically limited so far as the reaction proceeds. The compound of general formula (42) (R25 = a C1-3 alkyl group) may be hydrolyzed by the same procedure as described in step 26 to give the corresponding carboxylic acid.

The compounds of general formula (8, 11 , 12, 14, 15, 17, 18, 20, 21 , 28, 29, 30, 31 , 32, 33, 34, 36, 37, 38, 39, 40, 42) (R = a methoxymethyl group, a 2-(trimethylsilyl)ethoxymethyl group, a benzyl group, a p- methoxybenzyl group, a trimethylsilyl group, a triethylsilyl group, a t- butyldimethylsilyl group, a t-buthyldiphenylsilyl group or an acetyl group) may be subjected to deprotection in the presence of an acid, a base or a fluorine compound to give the compounds of general formula (8, 11 , 12, 14, 15, 17, 18, 20, 21 , 28, 29, 30, 31 , 32, 33, 34, 36, 37, 38, 39, 40, 42) (R = a hydrogen atom). Suitable acids for use in the deprotection step of the compounds of general formula (8, 11, 12, 14, 15, 17, 18, 20, 21 , 28, 29, 30, 31, 32, 33, 34, 36, 37, 38, 39, 40, 42) (R = a methoxymethyl group, a 2- (trimethylsilyl)ethoxymethyl group, a benzyl group, a p-methoxybenzyl group, a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a t- buthyldiphenylsilyl group) include hydrochloric acid, hydrobromic acid, sulfuric acid, acetic acid, phosphoric acid, trifluoroacetic acid, formic acid, 10-camphorsulfonic acid, p-toluenesulfonic acid, pyridinium p-toluenesuifonic acid, trifluoroborane-diethyl ether complex, methanesulfonic acid, acidic ion exchange resin. Suitable bases for use in the deprotection step of the compounds of general formula (8, 11 , 12, 14, 15, 17, 18, 20, 21 , 28, 29, 30, 31 , 32, 33, 34, 36, 37, 38, 39, 40, 42) (R = an acetyl group) include sodium hydroxide, potassium hydroxide, lithium hydroxide, potassium carbonate, sodium carbonate, sodium hydrogencarbonate, cesium carbonate. Suitable fluorine compounds for use in the deprotection step of the compounds of general formula (8, 11 , 12, 14, 15, 17, 18, 20, 21 , 28, 29, 30, 31 , 32, 33, 34, 36, 37, 38, 39, 40, 42) (R = a 2-(trimethylsilyl)ethoxymethyl group, a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a t-buthyldiphenylsilyl group or an acetyl group) include tetrabutylammonium fluoride, aqueous hydrogen fluoride, hydrogen fluoride-pyridine, hydrogen fluoride-triethylamine, potassium fluoride, sodium fluoride, calcium fluoride, cesium fluoride. Suitable solvents for use in the deprotection step of the compounds of general formula (8, 11 , 12, 14, 15, 17, 18, 20, 21 , 28, 29, 30, 31 , 32, 33, 34, 36, 37, 38, 39, 40, 42) (R = a methoxymethyl group, a 2- (trimethylsilyl)ethoxymethyl grou@, a benzyl group, a p-methoxybenzyl group, a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a t-buthyldiphenylsilyl group or an acetyl group) include hexane, benzene, toluene, diethyl ether, t-butyl methyl ether, tetrahydrofuran, 1 ,2- dimethoxyethane, 1 ,4-dioxane, diisopropyl ether, N,N-dimethylformamide, dimethylsulfoxide, N,N-dimethylacetamide, 1 ,3-dimethyl-2-imidazolidinone, 1 ,3-dimethyl-3,4,5,6-tetrahydro-2(1 H)-pyrimidinone, methanol, ethanol, isopropanol, acetonitrile, acetone, water, the mixtures. The reaction temperature in the deprotection step of the compounds of general formula (8, 11 , 12, 14, 15, 17, 18, 20, 21 , 28, 29, 30, 31 , 32, 33, 34, 36, 37, 38, 39, 40, 42) (R = a methoxymethyl group, a 2- (trimethylsilyl)ethoxymethyl group, a benzyl group, a p-methoxybenzyl group, a trimethylsilyl group, a triethylsilyl group, a t-butyldimethylsilyl group, a t- buthyldiphenylsilyl group or an acetyl group) is in the range from -50 °C to 200 °C, preferably from -20 0C to 120 0C, though it is not specifically limited so far as the reaction proceeds.

EXAMPLES To further illustrate this invention, the following examples are included. The examples should not, of course, be construed as specifically limiting the invention. Variations of these examples are within the purview of one skilled in the art and considered to fall within the scope of the invention as described and claimed herein. The reader will recognize that the skilled artisan, in possession of the present disclosure and skilled in the art, is able to prepare and use the invention without exhaustive examples. Materials used herein identified with trademarks are examples only and reflect illustrative materials used at the time of the invention. The skilled artisan will recognize that variations in lot, manufacturing processes, and the like, are expected. Hence the examples, and the trademarks used in them are non-limiting, and they are not intended to be limiting, but are merely an illustration of how a skilled artisan may choose to perform one or more of the embodiments of the invention. Reactions were performed under nitrogen or argon atmosphere at room temperature in stirring condition, otherwise indicated. Chromatographs were performed with nitrogen pressure using silica gel from Kanto Chemicals (silica gel 6ON (Spherical neutral) 40-50 micro m) or Merck (silica gel 60 (230-400 mesh ASTM) 40-50 micro m). Nuclear magnetic resonanse (NMR) analyses were performed on

AXR 300 (Bruker), a EX-270 sectrometer (JEOL), or Gemini2000/300

(Varian) in CDCI3 using tetramethylsilane as a internal standard, otherwise

indicated.

Mass spectrum (MS) analyses were performed on ZQ2000 (Waters),

LCQ Classic (Thermo), or Q-micro, Triple Quadrupole Mass Spectrometer

(MICROMASS) in APCI/ESI (atmospheric chemical pressure ionization/

electron spray ionization) negative or positive mode.

The following abbreviations have the indicated meanings:

(BoC)2O di-tert-butyl dicarbonate 1 ,25(OH)2D3 1a,25-dihydroxyvitamin D3 1 M 1 mol/l 1 N 1 normal Abu j^amma-aminobutyjic acid Ac2O acetic anhydride AcOEt ethyl acetate aq. aqueous BF3-OEt2 boron trifluoride diethyl etherate BnOH benzyl alcohol Boc tert-butoxycarbonyl CH3CN acetonitrile Cha beta-cyclohexylalanine Chg cyclohexylglycine chloroform-d CDCI3 cone concentrated CSA (1S)-(+)-10-camphorsulfonic acid DCC dicyclohexylcarbodiimide DEAD Diethyl azodicarboxylate Dess-Martin reagent 1 ,1 ,1-tris(acetyloxy)-1 ,1-dihydro-1 ,2- benziodoxol-3-(1 H)-one DHP dihydropyran DMAP 4-(dimethylamino)pyridine DMF N,N-Dimethylformamide DMSO dimethylsulfoxide dppp diphenylphosphinopropane EDC 1-ethyl-3-(3-dimethylaminopropyl)- cabodiimide Et ethyl Et2O diethylether Et3N Triethylamine Et3SiCI triethylsilyl chloride EtLi ethyl lithium EtMgBr ethyl magnesium bromide EtOAc ethyl acetate EtOH ethanol Fmoc 9-fluorenylmethoxycarbonyl Hex n-hexane HMPA hexamethylphosphoramide HOBT 1 -hydroxybenzotriazole HPLC high performance liquid chromatography J-Pr2EtN diisopropylethylamine i-PrOH, iPrOH isopropanol LAH lithium aluminum hydride LDA lithium diisopropylamide mCPBA m-chloroperbenzoic acid Me methyl MeCN acetonitrile MeOH methanol methanol-d4 CD3OD MOM methoxymethyl MS4A molecular sieves 4A MsCI methanesulfonyl chloride NaOMe sodium methoxide n-BuLi, nBuLi, BuLi n-butyl lithium n-Hex n-hexane NIe norleucine NMO N-methylmorpholine-N-oxide Nva norvaline ODS octadecylsilyl Orn ornitine PCC pyridinium chlorochromate Pd(OAc)2 Palladium acetate Pd(OH)2/C palladium hydroxide on carbon Pd(PPh3U tetrakis(triphenylphosphine)palladium Pd-C palladium on activated carbon PdCI2(dppf)2 bis(diphenylphosphino)ferrocene]palladium dichloride PdCI2(PPh3)2 dichlorobis(triphenylphosphine)palladium Phg phenylglycine Piv pivaloyl PPh3 triphenylphosphine PPTs pyridinium p-toluenesulfonate PTH parathyroid hormone pTsOH p-toluenesulfonic acid quant. quantitative yield rt room temperature sat. saturated TBAF tetrabutylammonium fluoride TBDMS tert-butyldimethylsilyl TBS tert-butyldimethylsilyl TBSCI tert-butyldimethylsilyl chloride TBSOTf tert-butyldimethysilyl trifluoromethanesulfonate tBu tert-butyl t-BuLi tert-butyl lithium t-BuNH2 tert-butylamine tBuOH tert-butylalcohol t-BuOK potassium tert-butoxide t-BuSH, tBuSH 2-methyl-2-propanethiol TEMPO 2,2,6,6-tetramethyl-1 -piperidinyloxy, free radical TES triethylsiliyl Tf trifluoromethanesulfonyl Tf2O Trifluoromethanesulfonic anhydride TFA trifluoroacetic acid THF Tetrahydrofuran THP tetrahydropyranyl TLC thin-layer chromatography TMS trimethylsilyl TMS-acetylene trimethylsilylacetylene TMSBr trimethylsilyl bromide Trt trityl Ts p-toluenesulfonyl v/v volume/volume Wang Resin p-hydroxymethyl-phenoxy-methylated polystylene WSCI 1-ethyl-3-(3-dimethylaminopropyl)- cabodiimide Example 1 Preparation of (S)-5-(4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

HOOC

(1) Preparation of trifluoro-methanesulfonic acid 4-[1 -ethyl-1 -(4-hydroxy-3- methyl-phenyl)-propyl]-2-methyl-phenyl ester

OTf

To a solution of 3,3-bis[4-hydroxy-3-methylphenyl]pentane (9.0 g, 31.6 mmol) in dichloromethane (300 ml), pyridine (3 ml, 37.2 mmol) and trifluoromethanesulufonic anhydride (5.7 ml, 34.7 mmol) were added at 0 °C and stirred at 0 °C for 1 h. To the mixture, ethylacetate was added and the organic layer was washed with saturated NaHCO3 solution and brine, dried over MgSO4, concentrated in vacuo, and chromatographed (ethylacetate/hexane = 1/10 to ethyl acetate only) to give the title compound (4.9 g, 37 %). 1H-NMR: 0.62 (t, 6H), 2.03 (q, 4H), 2.20 (s, 3H), 2.38 (s, 3H), 4.67 (s, 1H), 6.68 (d, 1 H), 6.80-6.88 (m, 2H), 7.02-7.11 (m, 3H); MS (ESI+) : 417 ([M+H]+).

(2) Preparation of 4-[1 -ethyl-1 -(3-methyl-4-trimethylsilanylethynyl-phenyl)- propyl]-2-methyl-phenol

^TMS To a solution of trifluoromethanesulfonic acid 4-[1 -ethyl- 1-(4-hydroxy-3- methyl-phenyl)-propyl]-2-methyl-phenyl ester (compound prepared in Example 1-(1)) (25 g, 60.03 mmol) in acetonitrile (300 ml), triethylamine (25.1 ml, 180.09mmol), ethynyltrimethylsilane (25.5 ml, 180.09 mmol), CuI (1.143 g, 6.00 mmol), and Pd(PPh3)4 (6.93 g, 6.00 mmol) were added. The mixture was stirred at 110 °C for 18 h and concentrated in vacuo. To the residue, ethylacetate and H2O added and the pH was adjusted at 7 by addition of 1 N HCI. The organic layer was dried over MgSO4, concentrated in vacuo, and chromatographed (ethylacetate/hexane = 1/15) to give the title compound (16 g, 74 %). 1H-NMR: 0.25 (s, 9H), 0.60 (t, 6H), 2.04 (q, 4H), 2.18 (s, 3H), 2.38 (s, 3H), 4.58 (s, 1H), 6.63 (d, 1H), 6.83-6.88 (m, 2H), 6.92 (d, 1H), 7.00 (s, 1H), 7.30 (d, 1 H).

(3) Preparation of 4-[1-ethyl-1-(4-ethynyl-3-methyl-phenyl)-propyl]-2-methyl- phenol

^TMS To a solution of 4-[1-ethyl-1-(3-methyl-4-trimethylsilanylethynyl-phenyl)- propyl]-2-methyl-phenol (compound prepared in Example 1-(2)) (19.03 g, 52.19 mmol) in THF (520 ml), 1 M terabutylanmonium fluoride in THF (78.3 ml, 78.3 mmol) was added. The mixture was stirred for 0.5 h, concentrated in vacuo, extracted with ethylacetate, washed with brine, dried over MgSO4, concentrated in vacuo, and chromatographed (ethylacetate/hexane = 1/10) to give the title compound (15.6 g, 94 %). 1H-NMR: 0.60 (t, 6H), 2.04 (q, 4H), 2.20 (s, 3H), 2.41 (s, 3H), 3.23 (s, 1 H), 4.51 (s, 1 H), 6.64 (d, 1H), 6.82-6.86 (m, 2H), 6.90-6.95 (m, 1 H), 7.00 (s, 1 H), 7.29 (d, 1 H); MS (ESI-) : 291 ([M-H]"). (4) Preparation of 4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

To a solution of 4-[1 -ethyl-1 -(4-ethynyl-3-methyl-phenyl)-propyl]-2-methyl- phenol (compound prepared in Example 1-(3)) (4.28 g, 14.69 mmol) in THF (92 ml), 2.5 M n-butyl lithium in hexane (14.7 ml, 36.73 mmol) was added at -78 °C. To the mixture, pentan-3-one (4.85 ml, 44.07 mmol) was added at - 78 °C, stirred at -78 °C for 3 h, and concentrated in vacuo. To the residue, ethylacetate and H2O were added and the pH was adjusted at 6 by addition of 1 N HCI. Extracted with ethylacetate, dried over Na2SO4, concentrated in vacuo, and chromatographed (ethylacetate/hexane = 1/6) to give the title compound (3.66 g, 62 %). 1H-NMR: 0.61 (t, 6H), 1.11 (t, 6H), 1.72-1.78 (m, 4H), 2.02 (q, 4H), 2.19 (s, 3H), 2.38 (s, 3H), 4.50 (s, 1H), 6.65 (d, 1H), 6.82-6.86 (m, 2H), 6.90-6.95 (m, 1 H), 7.00 (s, 1 H), 7.29 (d, 1 H); MS (ESI-): 377 ([M-H]").

(5) Preparation of 4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-(1 E)-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol

To a solution of 4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(4)) (800 mg, 2.11 mmol) in THF (8 ml), 1 M LiAIH4 in THF (5.28 ml, 5.28 mmol) was added. The mixture was refluxed for 18 h and H2O was added after cooling. Filtrated, extracted with ethylacetate, washed with brine, dried over MgSO4, concentrated in vacuo, and chromatographed (ethylacetate/hexane = 1/7) to give the title compound (500mg, 62%). 1H-NMR: 0.60 (t, 6H), 0.93 (t, 6H), 1.64 (q, 4H), 2.04 (q, 4H), 2.20 (s, 3H), 2.31 (s, 3H), 4.59 (s, 1H), 6.02 (d, 1H), 6.66 (d, 1H), 6.75 (d, 1H), 6.83-6.92 (m, 4H), 7.28 (d, 1 H) MS (ESI-) : 379 ([M-H]").

(6) Preparation of (S)-5-(4-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-fur an-2-one

To a solution of 4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-(1 E)-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1- (5)) (150 mg, 0.394 mmol) in dimethylformamide (4 ml), K2CO3 (136 mg, 0.985 mmol) was added and stirred for 0.5 h. To the mixture, toluene-4- sulfonic acid (S)-5-oxo-tetrahydro-furan-2-ylmethyl ester (160 mg, 0.591 mmol) was added and stirred at 100 °C for 15 h. After cooling to room temperature, saturated NH4CI solution was added. Extracted with ethylacetate, washed with brine, dried over MgSO4, concentrated in vacuo, and chromatographed (ethylacetate/hexane = 1/5 to 1/3) to give the title compound (170 mg, 90 %). 1H-NMR: 0.62 (t, 6H), 0.92 (t, 6H), 1.65 (q, 4H), 2.04 (q, 4H), 2.17 (s, 3H), 2.32 (s, 3H), 2.34-2.84 (m, 4H), 4.05-4.20 (m, 2H), 4.85-4.92 (m, 1 H), 6.02 (d, 1 H), 6.67 (d, 1 H), 6.75 (d, 1 H), 6.90-6.97 (m, 4H), 7.29 (d, 1 H); MS (ESI+) : 501 ([M+Na]+).

(7) Preparation of (S)-5-(4-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentano ic acid To a solution of (S)-5-(4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyclro-fura n-2-one (compound prepared in Example 1-(6)) (170 mg, 0.355 mmol) in methanol (7 ml), 1 N KOH solution (0.7 ml) was added. The mixture was stirred for 2 h, concentrated in vacuo, extracted with ethylacetate, washed with brine, dried over MgSO4, concentrated in vacuo, and chromatographed (dichloromethane/methanol = 20/1) to give the title compound (150 mg, 85 %). 1H-NMR (measured in CD3OD as potassium salt): 0.63 (t, 6H), 0.97 (t, 6H), 1.68 (q, 4H), 1.84-1.94 (m, 1H), 1.97-2.04 (m, 1 H), 2.10 (q, 4H), 2.21 (s, 3H), 2.32 (s, 3H), 2.42 (t, 2H), 3.93-4.03 (m, 3H), 6.04 (d, 1 H), 6.78 (d, 1 H), 6.81 (s, 1 H), 6.91 (s, 1 H), 6.95-7.00 (m, 3H), 7.31 (d, 1H); MS (ESI-) : 495 ([M-H]"

Example 2 Preparation of (S)-5-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-4-hydroxy- pentanoic acid

HOOC OH

(1 ) Preparation of 4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenol To a solution of 4-[1-ethyl-1-(4-ethynyl-3-methyl-phenyl)-propyl]-2-methyl- phenol (compound prepared in Example 1-(3)) (4.4 g, 15.1 mmol) in THF (108 ml), 2.5 M n-butyl lithium in hexane (12 ml, 30.2 mmol) was added at - 78 °C and stirred at -78 °C for 1h. To the mixture, hexafluoroacetone was passed by bubbling at -78 °C and stirred at -78 °C for 2 h. To the reaction mixture, diethylether and H2O were added, and the pH was adjusted at 7 by addition of 1 N HCI. Extracted with diethyl ether, dried over MgSO4, concentrated in vacuo, chromatographed two times (ethyl acetate/hexane = 1/10 and 1/5), and purified by HPLC (column:Merck Lobar column 40-63 micrometer 400x40 mm (ODS) , MeOH/H2O = 2/1 , 3/1 , and 4/1 , isocratic) to give the title compound (2.0 g, 29 %). 1H-NMR: 0.61 (t, 6H), 2.05 (q, 4H), 2.20 (s, 3H), 2.39 (s, 3H), 3.50 (s, 1H), 4.58 (s, 1 H), 6.66 (d, 1 H), 6.80-6.83 (m, 2H), 6.99 (d, 1 H), 7.07 (s, 1H), 7.34 (d, 1H).

(2) Preparation of 4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenol

F3C - ! F3C D_ To a solution of 4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 2-(1)) (356 mg, 0.777 mmol) in dimethylformamide (5 ml), K2CO3 (268 mg, 1.94 mmol) was added and stirred for 20min. To the mixture, chloromethoxymethane (71 μl, 0.935 mmol) was added and stirred for 1 h. To the reaction mixture, saturated NH4CI (20 ml) was added. Extracted with ethylacetate and dried over MgSO4, concentrated in vacuo, and chromatographed (ethylacetate/hexane = 1/6) to give the title compound (349 mg, 89 %). 1H-NMR: 0.60 (t, 6H), 2.05 (q, 4H), 2.20 (s, 3H), 2.40 (s, 3H), 3.49 (s, 3H), 4.59 (s, 1 H), 5.17 (s, 2H), 6.65 (d, 1 H), 6.80-6.83 (m, 2H), 6.99 (d, 1 H), 7.07 (s, 1 H), 7.38 (d, 1H).

(3) Preparation of (S)-5-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one

FsC O— 6 ' 3^ O— To a solution of 4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-methoxymethoxy- 3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-pheno l (compound prepared in Example 2-(2)) (300 mg, 0.597 mmol) in dimethylformamide (3 ml), 60 % NaH (29 mg, 0.725 mmol) was added and stirred for 0.5 h. To the mixture, toluene-4-sulfonic acid (S)-5-oxo-tetrahydro-furan-2-ylmethyl ester (194 mg, 0.719 mmol) was added and stirred at 110-120 °C for 16 h. To the reaction mixture, saturated NH4CI solution was added. Extracted with ethylacetate, washed with brine, dried over MgSO4, concentrated in vacuo, and chromatographed (ethylacetate/hexane = 1/3) to give the title compound (158 mg, 44 %). 1H-NMR: 0.60 (t, 6H), 2.05 (q, 4H), 2.17 (s, 3H), 2.42 (s, 3H), 2.25-2.80 (m, 4H), 3.49 (s, 3H), 4.04-4.17 (m, 2H), 4.86-4.92 (m, 1 H), 5.17 (s, 2H), 6.67 (d, 1H), 6.83 (s, 1 H), 6.92 (d, 1H), 6.98 (d, 1H), 7.02 (s, 1H), 7.38 (d, 1H). (4) Preparation of (S)-5-(4-{1-8thyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3 - trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-mθthyl-phenox ymethyl)-dihydro- furan-2-one

d ό- δ FsC To a solution of (S)-5-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 2-(3)) (338 mg, 0.562 mmol) in dichloromethane (10 ml), trifluoroacetic acid (1 ml) was added and stirred for 16 h. Concentrated in vacuo, and chromatographed (ethylacetate/hexane = 1/3) to give the title compound (153 mg, 49 %). 1H-NMR: 0.60 (t, 6H), 2.05 (q, 4H), 2.14 (s, 3H), 2.39 (s, 3H), 2.25-2.81 (m, 4H), 4.04-4.17 (m, 2H), 4.86-4.91 (m, 1H), 6.63 (d, 1H), 6.83 (s, 1H), 6.90 (dd, 1H), 6.96 (dd, 1 H), 7.02 (s, 1 H), 7.38 (d, 1H); MS (ESI-) : 555 ([M-H∏.

(5) Preparation of (S)-5-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3 - trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-4-hydroxy- pentanoic acid

HOO' Q- OH F3C To a solution of (S)-5-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3 - trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)-dihydro- furan-2-one (compound prepared in Example 2-(4)) (70.2 mg, 0.126 mmol) in ethanol (3 ml), 1 N KOH solution (0.378 ml) was added and stirred for 3 h. Concentrated in vacuo and extracted with diethylether. The pH was adjusted at 9 by addition of saturated KHSO4. The organic layer was filtrated through celite and concentrated in vacuo to give the title compound (36.7 mg, 52 %). 1H-NMR (measured in CD3OD as potassium salt): 0.60 (t, 6H), 1.77-1.88 (m, 1 H), 1.93-2.03 (m, 1H), 2.09 (q, 4H), 2.15 (s, 3H), 2.38 (s, 3H), 2.38-2.44 (m, 2H), 3.88-3.92 (m, 2H), 3.93-4.00 (m, 1H), 6.78 (d, 1H), 6.84 (s, 1H), 6.94 (dd, 1 H), 7.03 (d, 1 H), 7.09 (s, 1 H), 7.34 (d, 1 H); MS (ESI-) : 573 ([M-H]").

Example 3 Preparation of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

Preparation of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

To a solution of 4-[1 -ethyl-1 -(4-ethynyl-3-methyl-phenyl)-propyl]-2-methyl- phenol (compound prepared in Example 1-(3)) (12.22 g, 41.8 mmol) in THF (300 ml) was added 2.44 M n-butyl lithium in hexane (42.8 ml, 104.5 mmol) at 0 degrees C. The reaction mixture was stirred for 30min at 0 degrees C. Trimethylacetaldehyde (13.79 ml, 125.4 mmol) was added, stirred at 0 degrees C for 30min. To the reaction mixture, saturated aqueous NH4CI was added and extracted with ethyl acetate, washed with brine, dried over MgSO4, concentrated in vacuo, and chromatographed on silica gel (ethyl acetate/hexane= 10/90 to 25/75) to give the title compound (13.08 g, 83%). 1H-NMR(CDCI3): 0.59 (t, 6H), 1.07 (s, 9H), 1.86 (d, 1 H), 2.03 (q, 4H), 2.19 (s, 3H), 2.38 (s, 3H), 4.26 (d, 1H), 4.59 (s, 1 H), 6.65 (d, 1 H), 6.82-6.85 (m, 2H), 6.92-6.95 (m, 1 H), 7.00 (s, 1 H), 7.28 (d, 1H).

Example 4 Preparation of 4-{1 -ethyl-1 -[4-(3-hydroxy-3-propyl-hex-1 -ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

Preparation of 4-{1 -ethyl-1-[4-(3-hydroxy-3-propyl-hex-1-ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

Using the same procedure as described for the preparation of Example 3, the title compound was prepared from 4-[1-ethyl-1-(4-ethynyl-3-methyl- phenyl)-propyl]-2-methyl-phenol (compound prepared in Example 1-(3)). 1H-NMR(CDCI3): 0.60 (t, 6H), 0.92(t, 3H), 1.30-1.61(m, 8H),2.05(q, 4H), 2.19(s,3H), 2.30(s,3H), 4.70(s, 1H), 6.65(d, 1H), 6.83(m, 2H), 7.00(d,1H), 7.18(d, 1 H), 7.28(d, 1 H); MS (ESI-) : 405 ([M-H∏-

Example 5 Preparation of 4-{1 -ethyl-1 -[4-(3-hydroxy-3-methyl-but-1 -ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol Preparation of 4-{1 -ethyl-1 -[4-(3-hydroxy-3-methyl-but-1 -ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

Using the same procedure as described for the preparation of Example 3, the title compound was prepared from 4-[1-ethyl-1-(4-ethy nyl-3-methyl- phenyl)-propyl]-2-methyl-phenol (compound prepared in Example 1-(3)). 1H-NMR(CDCI3): 0.59 (t, 6H), 1.62(s,6H), 2.02(q,4H), 2.05(s, 1H)1 2.18(s,3H), 2.36(s,3H), 4.60(bs, 1 H), 6.63-7.00(m, 5H), 7.26(d, 1 H).

Example 6 Preparation of 4-{1 -ethyl-1 -[4-(1 -hydroxy-cyclobutylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

Preparation of 4-{1 -ethyl-1 -[4-(1 -hydroxy-cyclobutylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol Using the same procedure as described for the preparation of Example 3, the title compound was prepared from 4-[1-ethyl-1-(4-ethynyl-3-methyl- phenyl)-propyl]-2-methyl-phenol (compound prepared in Example 1-(3)). 1H-NMR(CDCI3): 0.61 (t, 6H), 1.81-2.05(m, 6H), 2.01(q, 4H), 2.18(s, 3H), 2.36(s, 3H), 4.86(s, 1H)1 6.65(d, 1 H), 6.82(dd, 1H), 6.84(s, 1H),6.93(dd, 1 H), 7.00(d,1 H), 7.26(d, 1 H); MS (ESI-) : 361 ([M-H∏-

Example 7 Preparation of 4-{1 -ethyl-1 -[4-(1 -hydroxy-cyclopentylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

Preparation of 4-{1 -ethyl-1 -[4-(1 -hydroxy-cyclopentylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

Using the same procedure as described for the preparation of Example 3, the title compound was prepared from 4-[1-ethyl-1-(4-ethynyl-3-methyl- phenyl)-propyl]-2-methyl-phenol (compound prepared in Example 1-(3)). 1H-NMR(CDCI3): 0.59 (t, 6H), 1.68-1.91(m,4H), 1.99-2.10(m, 4H), 2.01(q, 4H), 2.18(s,3H), 2.36(s,3H), 4.86(s, 1 H), 6.65(d, 1 H), 6.82(dd, 1 H), 6.84(s, 1 H)1 6.93(dd, 1 H), 7.00(d,1 H), 7.26(d, 1 H); MS (ESI-) : 375 ([M-H]").

Example 8 Preparation of 4-{1 -ethyl-1 -[4-(1 -hydroxy-cyclohexylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol Preparation of 4-{1 -ethyl-1 -[4-(1 -hydroxy-cyclohexylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

H( Using the same procedure as described for the preparation of Example 3, the title compound was prepared from 4-[1-ethyl-1-(4-ethynyl-3-methyl- phenyl)-propyl]-2-methyl-phenol (compound prepared in Example 1-(3)). 1H-NMR(CDCI3): 0.59 (t, 6H), 1.52-179(m, 7H), 1.92-2.08(m, 4H), 2.02(q, 4H), 2.18(s,3H), 2.38(s,3H), 4.58(s, 1 H), 6.64(d, 1 H), 6.84(dd, 1 H), 6.86(s, 1 H) ,6.94(dd, 1 H), 7.00(s, 1 H), 7.28(d, 1H); MS (ESI-) : 389 ([M-H]").

Example 9 Preparation of 4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenol

Preparation of 4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenol To a solution of 4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 2-(1)) (0.5 g, 1.09 mmol) in THF (10 ml) was slowly added LiAIH4 (1 M in THF) (4.22 ml, 4.226 mmol) at 25 degrees C. The reaction mixture was refluxed for 2 h. The reaction mixture was cooled to 0 degrees C. To the mixture, saturated aqueous NH4CI was added and extracted with diethyl ether. The mixture was filtered through celite, washed with brine, dried over Na2SO4, concentrated in vacuo, and chromatographed on silica gel (hexane/dichloromethane/ethyl acetate=1/10/1) to give the title compound (0.4 g, 80%). 1H NMR (CDCI3): 7.39(s, 1H), 7.34(t, 1 H), 7.00(d, 1 H), 6.99(s, 1 H), 6.91- 6.84(m, 2H), 6.65(d, 1 H), 6.10(d, 1H), 4.52(s, 1 H), 3.11 (s, 1H), 2.33(s, 3H), 2.25(s, 3H), 2.04(q, 4H), 0.59(t, 6H).

Example 10 Preparation of 4-(1 -ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclopentyl)-vinyl]-3-methyl- phenyl}-propyl)-2-methyl-phenol

Preparation of 4-(1 -ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclopentyl)-vinyl]-3-methyl- phenyl}-propyl)-2-methyl-phenol

Using the same procedure as described for the preparation of Example 9, the title compound was prepared from 4-{1 -ethyl-1 -[4-(1-hydroxy- cyclopentylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 7). 1H-NMR(CDCI3): 0.60(t, 6H), 0.92(t,3H), 1.68-1.91 (m,4H), 1.99-2.10(m, 4H), 2.04(q, 4H), 2.19(s,3H), 2.31(s,3H), 4.58(s, 1H), 6.26(d, 1H), 6.64(d, 1H)1 6.81-6.96(m, 5H), 7.32(d, 1H); MS (ESI-) : 377 ([M-H]").

Example 11 Preparation of 4-(1 -ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclohexyl)-vinyl]-3-methyl- phenyl}-propyl)-2-methyl-phenol

Preparation of 4-(1 -ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclohexyl)-vinyl]-3-methyl- phenyl}-propyl)-2-methyl-phenol

Using the same procedure as described forthe preparation of Example 9, the title compound was prepared from 4-{1 -ethyl-1 -[4-(1-hydroxy- cyclohexylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 8). 1H-NMR(CDCI3): 0.60 (t, 6H), 1.33-1.74(m, 10H)1 2.04(q, 4H), 2.23(s,3H), 2.31(s,3H), 4.68(S, 1 H), 6.23(d, 1 H), 6.65(d, 1H), 6.79-7.00(m, 5H) ,7.31(d, 1 H); MS (ESI-) : 391 ([M-H]").

Example 12 Preparation of 4-{1 -ethyl-1 -[4-((E)-3-hydroxy-3-methyl-but-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol Preparation of 4-{1 -ethyl-1 -[4-((E)-3-hydroxy-3-methyl-but-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

Using the same procedure as described forthe preparation of Example 9, the title compound was prepared from 4-{1 -ethyl-1-[4-(3-hydroxy-3-methyl- but-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 5). 1H-NMR(CDCI3): 0.60 (t, 6H), 1.42(s, 6H), 2.05(q, 4H), 2.18(s, 3H), 2.30(s, 3H), 4.97(s, 1 H), 6.22(d, 1 H), 6.64(d, 1 H), 6.76(d, 1 H), 6.84-6.90(m, 2H), 6.94-6.97(m, 2H), 7.31(d, 1H); MS (ESI-) : 351 ([M-H]").

Example 13 Preparation of 4-{1 -ethyl-1 -[4-((E)-3-hydroxy-3-propyl-hex-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

Preparation of 4-{1 -ethyl-1 -[4-((E)-3-hydroxy-3-propyl-hex-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

Using the same procedure as described for the preparation of Example 9, the title compound was prepared from 4-{1 -ethyl-1 -[4-(3-hydroxy-3-propyl- hex-1 -ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 4). 1H-NMR(CDCI3): 0.61 (t, 6H), 0.92(t, 3H), 1.32-1.50(m, 3H), 1.54~1.64(m, 5H), 2.03(q, 4H), 2.19(s,3H), 2.30(s,3H), 4.71(s, 1 H), 6.06(d, 1H), 6.69(d, 1 H), 6.75(d, 1 H), 6.85~6.96(m, 4H), 7.32(d, 1 H); MS (ESI-) : 407 ([M-H]").

Example 14 Preparation of 4-{1 -ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol

Preparation of 4-{1 -ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol

OH

Using the same procedure as described for the preparation of Example 9, the title compound was prepared from 4-{1-ethyl-1-[4-(3-hydroxy-4, 4- dimethyl-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phen ol (compound prepared in Example 3). 1H-NMR(CDCI3): 0.60 (t, 6H), 0.96 (s, 9H), 2.03(q, 4H), 2.19(s, 3H), 2.29(s, 3H), 3.92(d, 1 H), 6.12(dd, 1 H), 6.65(d, 1 H), 6.73(d, 1 H), 6.84-6.97(m, 4H)1 7.31 (d, 1H); MS (ESI-) : 379 ([M-H]").

Example 15 Preparation of 4-(1 -ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclobutyl)-vinyl]-3-methyl- phenyl}-propyl)-2-methyl-phenol Preparation of 4-(1 -ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclobutyl)-vinyl]-3-methyl- phenyl}-propyl)-2-methyl-phenol

OH

Using the same procedure as described for the preparation of Example 9, the title compound was prepared from 4-{1-ethyl-1-[4-(1-hydroxy- cyclobutylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 6). 1H-NMR(CDCI3): 0.61 (t, 6H), 1.54-1.91(m, 3H), 2.05(q, 4H), 2.18(s,3H), 2.30(m, 3H), 2.32(s, 3H), 4.75(s, 1 H), 6.47(d, 1 H), 6.68(d, 1 H), 6.81-7.00(m, 5H), 7.39(d, 1 H).

Example 16 Preparation of 2-chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)- phenyl]-1-ethyl-propyl}-phenol (Enantiomer 1)

(1) Preparation of trifluoro-methanesulfonic acid 2-chloro-4-[1 -(3-chloro-4- hydroxy-phenyl)-1 -ethyl-propyl]-phenyl ester

U

HO' O+° + H Cl Cl Cl To a mixture of 2-chlorophenol (12.86 g, 100 mmol) and 3-pentanone (5.30 ml, 50 mmol), trifluoromethane sulfonic acid (3.1 ml, 35 mmol) was added and stirred for 17hr at 90 degrees C. The reaction mixture was chromatographed on silica gel (ethyl acetate/hexane = 0/100 to 17/83) to give the brown foam (324 mg). The foam was dissolved with CH2CI2 (5 ml) and pyridine (0.097 ml, 1.2 mmol), trifluoromethane sulfonic anhydride (0.185ml, 1.1 mmol) was added and stirred for 1.5h at 0 degrees C. To the reaction mixture, aqueous KHSO4 was added and extracted with ethyl acetate, washed with brine, dried over MgSO4, concentrated in vacuo, and ( chromatographed on silica gel (ethyl acetate/hexane = 0/100 to 18/82) to give the title compound (117mg, 0.5%). 1H-NMR: 0.63 (t, 6H), 2.04 (q, 4H), 5.46 (s, 1H), 6.90-7.34 (m, 6H); MS(ESI-) : 455([M-H∏.

(2) Preparation of 2-chloro-4-[1 -(3-chloro-4-trimethylsilanylethynyl-phenyl)-1 - ethyl-propyl]-phenol

Il Cl Cl Cl ^TMS To a solution of trifluoro-methanesulfonic acid 2-chloro-4-[1-(3-chloro-4- hydroxy-phenyl)-1-ethyl-propyl]-phenyl ester (compound prepared in Example 16-(1 )) (117mg, 0.256 mmol) in MeCN (1 ml) was added trimethylsilylacethylene (0.109 ml, 0.768 mmol), Pd(PPh3)4 (30mg, 0.026 mmol), CuI (5mg, 0.026 mmol) and triethylamine (0.107mL, 0.768 mmol) were added and stirred for 1 h at 100 degrees C under nitrogen atmosphere. To the reaction mixture, saturated aqueous NH4CI was added and extracted with ethyl acetate, washed with H2O twice, dried over MgSO4, concentrated in vacuo, and chromatographed on silica gel (ethyl acetate/hexane = 0/100 to 15/85) to give the title compound (27mg, 26%). 1H-NMR: 0.26 (s, 9H), 0.61 (t, 6H), 2.01 (q, 4H), 5.35-5.45 (brs, 1H), 6.88- 7.39 (m, 6H). (3) Preparation of 2-chloro-4-[1-(3-chloro-4-ethynyl-phenyl)-1-ethyl-propyl]- phenol

Cl Cl -TMS Cl c, --H To a solution of 2-chloro-4-[1-(3-chloro-4-trimethylsilanylethynyl-phenyl)-1- ethyl-propyl]-phenol (compound prepared in Example 16-(2)) (27 mg, 0.067 mmol) in THF (0.5 ml) was added 1 M TBAF in THF (0.33 ml, 0.33 mmol) at room temperature. The reaction mixture was allowed for 3min. To the reaction mixture, aqueous KHSO4 was added and extracted with ethyl acetate/hexane=1/1 , washed with aqueous NaHCO3, aqueous KHSO4, aqueous NaHCO3, aqueous KHSO4, aqueous NaHCO3, successively, dried over MgSO4, concentrated in vacuo to give the title compound (20mg, 90%). 1H-NMR: 0.62 (t, 6H), 2.03 (q, 4H), 3.33 (s, 1H), 6.90-7.41 (m, 6H).

(4) Preparation of 2-chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pent-1- ynyl)-phenyl]-1-ethyl-propyl}-phenol

H To a solution of 2-chloro-4-[1-(3-chloro-4-ethynyl-phenyl)-1-ethyl-propyl]- phenol (compound prepared in Example 16-(3)) (20 mg, 0.06 mmol) in THF (0.6 ml) was added 1.59 M n-butyl lithium in hexane (0.094 ml, 0.15 mmol) at 0 degrees C. The reaction mixture was stirred for 30min at 0 degrees C. trimethylacetaldehyde (0.020 ml, 0.18 mmol) was added, stirred at 0 degrees C for 30min. To the reaction mixture, saturated aqueous NH4CI was added and extracted with ethyl acetate, washed with brine, dried over MgSO4, concentrated in vacuo, and chromatographed on silica gel (ethyl acetate/hexane=1/5) to give the title compound (15 mg, 60%). 1H-NMR: 0.62 (t, 6H), 1.08 (s, 9H), 2.02 (q, 4H), 4.26 (s, 1 H), 6.90-6.98 (m, 3H), 7.09-7.21 (m, 2H), 7.35 (d, 1H).

(5) Chiral separation of 2-chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl- pent-1 -ynyl)-phenyl]-1 -ethyl-propyl}-phenol

Enantiomer A Enantiomer B Racemic mixture of 2-chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl- pent-1-ynyl)-phenyl]-1-ethyl-propyl}-phenol (compound prepared in Example 16-(4)) (15 mg, 0.036 mmol) was separated with HPLC (CHIRALPAK OJ [DAICEL, 20 mm I.D., 250 mm], Ethanol/hexane = 15/85), to give each enantiomer (Enantiomer A : 6 mg / Enantiomer B : 6 mg). Enantiomer A Column: CHIRALPAK OJ-RH 4.6*150 mm (DAICEL) Eluent: Hexane/EtOH=85/15 Temperature: 35 degrees C. Flow rate: 1.0 ml/min. Retention time: 4.1 min. Enantiomer B Retention time: 6.1 min.

(6) Preparation of 2-chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)- phenyl]-1-ethyl-propyl}-phenol (Enantiomer 1)

Cl To a solution of 2-chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pent-1- ynyl)-phenyl]-1-ethyl-propyl}-phenol (Enantiomer A prepared in Example 16- (5)) (6 mg, 0.014 mmol) in ethyl acetate (1 ml), 10% Pd-C (1 mg) was added and the mixture was stirred under hydrogen atmosphere for 90min. The reaction mixture was filtered and concentrated in vacuo to give the title compound (6 mg, 99 %). 1H-NMR: 0.62 (t, 6H), 0.89 (s, 9H), 1.43-1.59 (m, 1 H), 1.81-1.92 (m, 1 H), 2.02 (q, 4H), 2.66-2.76 (m, 1 H), 2.92-3.02 (m, 1 H)1 3.21-3.25 (m, 1 H), 5.40 (s, 1 H), 6.88-6.95 (m, 3H), 7.10-7.15 (m, 3H).

Example 17 Preparation of 2-chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)- phenyl]-1-ethyl-propyl}-phenol (Enantiomer 2)

>\ OH Preparation of 2-chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)- phenyl]-1-ethyl-propyl}-phenol (Enantiomer 2)

)H Ol C ulι OH To a solution of 2-chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pent-1- ynyl)-phenyl]-1-ethyl-propyl}-phenol (Enantiomer B prepared in Example 16- (5)) (6 mg, 0.014 mmol) in ethyl acetate (1 ml), 10% Pd-C (1 mg) was added and the mixture was stirred under hydrogen atmosphere for 90min. The reaction mixture was filtered and concentrated in vacuo to give the title compound (6 mg, 99 %). 1H-NMR: 0.62 (t, 6H), 0.89 (s, 9H), 1.43-1.59 (m, 1 H), 1.81-1.92 (m, 1 H), 2.02 (q, 4H), 2.66-2.76 (m, 1 H), 2.92-3.02 (m, 1 H), 3.21-3.25 (m, 1 H), 5.40 (s, 1 H), 6.88-6.95 (m, 3H), 7.10-7.15 (m, 3H). Example 17 Preparation of 2-chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)- phenyl]-1-ethyl-propyl}-phenol (Enantiomer 2)

Cl H Preparation of 2-chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)- phenyl]-1-ethyl-propyl}-phenol (Enantiomer 2)

Cl OH cι cι OH To a solution of 2-chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pent-1- ynyl)-phenyl]-1-ethyl-propyl}-phenol (Enantiomer B prepared in Example 16- (5)) (6 mg, 0.014 mmol) in ethyl acetate (1 ml), 10% Pd-C (1mg) was added and stirred under hydrogen atmosphere for 90min. The reaction mixture was filtered and concentrated under vacuum to give the title compound (6 mg, 99 %). 1H-NMR: 0.62 (t, 6H), 0.89 (s, 9H), 1.43-1.59 (m, 1 H), 1.81-1.92 (m, 1 H), 2.02 (q, 4H), 2.66-2.76 (m, 1 H), 2.92-3.02 (m, 1 H), 3.21-3.25 (m, 1 H), 5.40 (s, 1 H), 6.88-6.95 (m, 3H), 7.10-7.15 (m, 3H).

Example 18 Preparation of 4-{1 -ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

(1 ) Preparation of (E)-3-{4-[1-ethyl-1-(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenylj-acrylic acid methyl ester Trifluoromethanesulfonic acid 4-[1 -ethyl-1 -(4-hydroxy-3-methyl-phenyl)- propyl]-2-methyl-phenyl ester (compound prepared in Example 1-(1)) (10 g, 24.0 mmol) was dissolved in anhydrous DMF (70 ml) under nitrogen atmosphere. To this solution were added triethylamine (4.0 ml, 28.8 mmol), methylacrylate (2.6 ml, 28.8 mmol), 1 ,3-bis(diphenylphosphine)propane (544 mg, 1.32 mmol) and palladium acetate (269 mg, 1.2 mmol) at room temperature. After stirring 1.5 h at 100 degrees C, the resulting solution was diluted with CH2CI2, and washed with 5% HCI solution and water until neutrality was achieved, and dried over Na2SO4. The solution was evaporated under reduced pressure and purified by silica-gel column (hexane/ethyl acetate=7:1) to yield the title compound (7.6 g, 21.5 mmol, 90%). 1H NMR (CDCI3): 7.94 (d, 1 H), 7.42 (d, 1 H), 7.00 (m, 2H), 6.85 (m, 2H), 6.65 (d, 1 H), 6.32 (d, 1 H), 4.70 (s, phenol), 3.79 (s, 3H), 2.38 (s, 3H), 2.19 (s, 3H), 2.04 (q, 4H), 0.60 (t, 6H).

(2) Preparation of 3-{4-[1-ethyl-1-(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenyl}-propionic acid methyl ester

"OO2CH3 HO Y T ^ XO2CH3

(E)-3-{4-[1 -Ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2-methyl-phenyl}- acrylic acid methyl ester (compound prepared in Example 18-(1)) (270 mg, 0.76 mmol) was dissolved in methanol (7 ml). To this solution was added palladium carbon (10 mg), and stirred at room temperature under hydrogen gas overnight. The resulting solution was filtered through celite, and the filtrate was evaporated under reduced pressure and purified by silica-gel chromatography (hexane/ethyl acetate=10:1) to give the title compound (266 mg, 0.75 mmol, 98%). 1H NMR (CDCI3): 6.99-6.83 (m, 5H), 6.64 (d, 1 H), 4.54 (s, phenol), 3.67 (s, 3H), 2.89 (dt, 2H), 2.57 (dt, 2H), 2.24 (s, 3H), 2.19 (s, 3H), 2.02 (q, 4H), 0.59 (t, 6H).

(3) Preparation of 1 -{4-[1 -ethyl-1-(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenyl}-4,4-dimethyl-pentan-3-one

CO2CH3

3-{4-[1-Ethyl-1-(4-hydroxy-3-methyl-phenyl)-propyl]-2-met hyl-phenyl}- propionic acid methyl ester (compound prepared in Example 18-(2)) (3.0 g, 8.46 mmol) was dissolved in anhydrous THF (80 ml) under nitrogen atmosphere. The solution was cooled to -78 degrees C. To this solution was added t-BuLi (4.97 ml, 8.46 mmol, 1.7M in pentane) at -78 degrees C. After stirring 30min at -78 degrees C, the solution was diluted with dichloromethane, and washed with saturated NH4CI aq., water and brine, and dried over Na2SO4. The solution was evaporated under reduced pressure and purified by silica-gel chromatography (hexane/ethyl acetate=7:1) to give the title compound (2.5 g, 6.56 mmol, 77%). 1H NMR (CDCI3): 7.03-6.83 (m, 5H), 6.64 (d, 1 H), 4.60 (s, phenol), 2.82 (dt, 2H), 2.71 (dt, 2H), 2.24 (s, 3H), 2.18 (s, 3H), 2.04 (q, 4H), 1.09 (s, 9H), 0.58 (t, 6H).

(4) Preparation of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

O ' ' OH 1 -{4-[1 -Ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2-methyl-phenyl}-4,4- dimethyl-pentan-3-one (compound prepared in Example 18-(3)) (200 mg, 0.52 mmol) was dissolved in methanol (5 ml) under nitrogen atmosphere. To this solution was added sodium borohydride (29.8 mg, 0.78 mmol) at 0 degrees C. After stirring 1.0 h at room temperature, the solution was evaporated under reduced pressure and the obtained residue was purified by silica-gel chromatography (hexane/ethyl acetate=7:1) to give the title compound (190 mg, 0.50 mmol, 95%). 1H NMR (CDCI3): 7.03-6.83 (m, 5H), 6.63 (d, 1 H), 4.99 (s, phenol), 3.25 (dt, 1 H), 2.86 (m, 1H), 2.55 (m, 1 H), 2.24 (s, 3H), 2.18 (s, 3H), 2.03 (q, 4H), 1.79 (m, 1 H), 1.50 (m, 1 H), 0.89 (s, 9H), 0.59 (t, 6H).

Example 19 Preparation of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (Enantiomer 1 )

)H (1) Chiral separation of 4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenol

Enantiomer A Enantiomer B Racemic mixture of 4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 3) (13.08 g, 34.6 mmol) was separated with HPLC (CHIRALPAK AD [DAICEL, 20 mm I. D., 250 mm], 2-propanol/hexane = 15/85), to give each enantiomer (Enantiomer A : 99.9% ee, 5.58g / Enantiomer B : 5.0Og, 99.4%ee). Enantiomer A Column: CHIRALPAK AD-H 4.6x150 mm (DAICEL) Eluent: Hexane/2-propanol=85/15 Flow rate: 1.0 ml/min. Retention time: 5.1 min. Enantiomer B Retention time: 7.2 min.

(2) Preparation of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (Enantiomer 1 )

To a solution of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol (Enantiomer A prepared in Example 19-(1)) (796 mg, 2.1 mmol) in ethyl acetate (10 ml), 10% Pd-C (0.1 g) was added and stirred under hydrogen atmosphere for 40min. The reaction mixture was filtered and concentrated in vacuo to give the title compound (732 mg, 91%). 1H-NMR: 0.60 (t, 6H), 0.89 (s, 9H), 1.40 (d, 1H), 1.44-1.55 (m, 1 H), 1.74- 1.85 (m, 1 H), 2.03 (q, 4H), 2.19 (s, 3H), 2.25 (s, 3H), 2.51-2.61 (m, 1 H), 2.81-2.91 (m, 1 H), 3.25 (dd, 1 H), 4.59 (s, 1 H), 6.64 (d, 1 H), 6.85-7.00 (m, 4H), 7.03 (d, 1 H).

Example 20 Preparation of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (Enantiomer 2)

H

Preparation of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (Enantiomer 2) H To a solution of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol (Enantiomer B prepared in Example 19-(1 )) (725 mg, 1.92 mmol) in ethyl acetate (10 ml), 10% Pd-C (0.1 g) was added and stirred under hydrogen atmosphere for 40 min. The reaction mixture was filtered and concentrated in vacuo to give the title compound (720 mg, 98%). 1H-NMR: 0.60 (t, 6H), 0.89 (s, 9H), 1.40 (d, 1 H), 1.44-1.55 (m, 1 H), 1.74- 1.85 (m, 1 H), 2.03 (q, 4H), 2.19 (s, 3H), 2.25 (s, 3H), 2.51-2.61 (m, 1 H), 2.81-2.91 (m, 1H), 3.25 (dd, 1H), 4.59 (s, 1H), 6.64 (d, 1 H), 6.85-7.00 (m, 4H), 7.03 (d, 1 H).

Example 21 Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(3-hydroxy-3-methyl-but-1 -ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

o HO

(1) Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(3-hydroxy-3-methyl-but-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

o- 0H Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1 -ethyl-1 -[4-(3-hydroxy-3- methyl-but-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 5). The yield was 58%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.57 (s, 6H), 2.09 (q, 4H), 2.16 (s, 3H), 2.26 (m, 1 H), 2.34 (s, 3H), 2.39-2.62 (m, 3H), 2.71-2.82 (m, 1H), 4.06 (dd, 1H), 4.14 (dd, 1 H), 4.84-4.91 (m, 1H),, 6.69 (d, 1H), 6.89 (m, 2H), 6.95 (d, 1 H), 7.00 (s, 1 H), 7.27 (d, 1 H).

(2) Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(3-hydroxy-3-methyl-but-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

o

OH O' wn OH Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1 -ethyl- 1-[4-(3-hydroxy- 3-methyl-but-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)- dihydro-furan-2-one (compound prepared in Example 21 -(1 )). The yield was 71 %. 1H-NMR (300MHz, CD3OD as potassium salt): 0.60 (t, 6H), 1.57 (s, 6H), 1.79-2.02 (m, 2H), 2.04 (q, 4H), 2.16 (s, 3H), 2.34 (s, 3H), 2.35 (td, 2H), 3.90-3.93 (m, 3H), 6.77 (d, 1 H), 6.84 (s, 1 H), 6.94 (dd, 2H), 7.00 (s, 1 H), 7.21 (d, 1 H); MS(ESI-) : m/z: 465 ([M-H]").

Example 22 Preparation of (S)-5-(4-{1 -ethyl-1 -[4-((E)-3-hydroxy-3-methyl-but-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

o HO = OH

(1) Preparation of (S)-5-(4-{1 -ethyl-1 -[4-((E)-3-hydroxy-3-methyl-but-1-enyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-fur an-2-one

OH _ OH HO Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1-ethyl-1-[4-((E)-3-hydroxy-3- methyl-but-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 12). The yield was 44%. 1H-NMR (300MHz, CDCI3): 0.57 (t, 6H), 1.42 (s, 6H), 2.05 (q, 4H), 2.20 (s, 3H), 2.29 (m, 1 H), 2.34 (s, 3H), 2.39-2.62 (m, 3H), 2.71-2.82 (m, 1 H), 4.06 (dd, 1 H), 4.14 (dd, 1 H), 4.84-4.91 (m, 1 H), 6.16 (d, 1 H), 6.72 (s, 1 H), 6.76 (d, 1 H), 6.83 (s, 1 H), 6.91-6.95 (m, 3H), 7.32 (d, 1 H).

(2) Preparation of (S)-5-(4-{1-ethyl-1-[4-((E)-3-hydroxy-3-methyl-but-1-enyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentano ic acid

o "HO^^^Y^O = OH OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1-ethyl-1-[4-((E)-3- hydroxy-3-methyl-but-1-enyl)-3-methyl-phenyl]-propyl}-2-meth yl- phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 22- (1 )). The yield was 90%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.60 (t, 6H), 1.57 (s, 6H), 1.82-2.01 (m, 2H), 2.05 (q, 4H), 2.13 (s, 3H), 2.25 (s, 3H), 2.37 (td, 2H), 3.90- 3.93 (m, 3H), 6.16 (d, 1 H), 6.72 (s, 1 H), 6.76 (d, 1 H), 6.83 (s, 1 H), 6.90-6.95 (m, 3H), 7.27 (d, 1 H); MS(ESI-) : 467 ([M-H]").

Example 23 Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

HOOC OH (1) Preparation of (S)-5-(4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

OH OH

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy- pent-1 -ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(4)). The yield was 56%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.11 (t, 6H), 1.72-1.81 (q, 4H), 2.03 (q, 4H), 2.14 (s, 3H), 2.37 (s, 3H), 2.28-2.62 (m, 3H), 2.72-2.85 (m, 1 H), 4.04-4.19 (m, 2H), 4.89 (m, 1 H), 6.65 (d, 1 H), 6.87 (d, 2H), 6.91 (s, 1 H), 6.98 (s, 1 H), 7.27 (d, 1 H).

(2) Preparation of (S)-5-(4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

C^0 HOOC OH OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1-ethyl-1-[4-(3-ethyl-3- hydroxy-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)- dihydro-furan-2-one (compound prepared in Example 23-(1)). The yield was 76%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.11 (t, 6H), 1.72-1.81 (m, 4H), 1.87-1.98 (m, 2H), 2.03 (q, 4H), 2.16 (s,3H), 2.37 (s,3H), 2.62 (t, 2H), 3.82- 3.87 (dd, 1 H), 3.95-3.99 (dd, 1 H), 4.05-4.11 (m, 1 H), 6.67 (d, 1 H), 6.86 (s, 1 H), 6.90 (s, 1 H), 6.94 (d,1 H), 6.99 (d, 1 H), 7.27 (d, 1 H); MS(ESI-) : 493 ([M-H]"). Example 24 Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

HOOC^ OH Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

HOOCv ^^V HOOC

To a solution of (S)-5-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid (compound prepared in Example 23-(2)) (50 mg, 0.101 mmol) in EtOH (10 ml) was added Pd(OH)2 (10 mg) and the mixture was stirred under hydrogen gas at room temperature for 12 h. The reaction mixture was filtered through celite. and concentrated in vacuo. The crude mixture (40 mg) was dissolved in MeOH (7 ml). 1 N-KOH (0.3 ml, 0.30 mmol) was added at room temperature and the mixture was stirred for 4 h. The reaction mixture was concentration in vacuo, diluted with EtOAc, washed with brine, dried over MgSO4, filtered, and concentration in vacuo. The obtained residue was purified by silica gel chromatography eluting with CH2CI2/ EtOAc (20:1) to give the title compound (26 mg, 52%) as a white solid. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.91 (t, 6H), 1.51-1.59 (m, 4H), 1.63-1.69 (m, 2H), 1.88-1.96 (m, 2H), 2.00-2.07 (q, 4H), 2.17 (s,3H), 2.25 (s,3H), 2.54-2.65 (m, 4H), 3.82-3.87 (dd, 1 H), 3.95-3.99 (dd, 1 H), 4.05-4.11 (m, 1 H), 6.67 (d, 1 H), 6.86 (d, 1 H), 6.89-7.01 (m, 5H); MS (ESI-) : 497 ([M- H]-).

Example 25 Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(3-hydroxy-3-propyl-hex-1 -ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

o OH OH

(1) Preparation of (S)-5-(4-{1-ethyl-1-[4-(3-hydroxy-3-propyl-hex-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

OH OH

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1-ethyl-1-[4-(3-hydroxy-3- propyl-hex-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 4). The yield was 78%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.98 (t, 6H), 1.54-1.74 (m, 8H), 2.02 (q, 4H), 2.14 (s, 3H), 2.26 (m, 1 H), 2.36 (s, 3H), 2.39-2.62 (m, 3H), 2.71-2.82 (m, 1 H), 4.06 (dd, 1 H), 4.14 (dd, 1 H), 4.87 (m, 1 H), 6.65 (d, 1 H), 6.87 (s, 1 H), 6.95 (dd, 2H), 6.98 (s, 1 H), 7.27 (d, 1 H).

(2) Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(3-hydroxy-3-propyl-hex-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

o OH HO^ — ^Y^O OH OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1 -ethyl-1 -[4-(3-hydroxy- 3-propyl-hex-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)- dihydro-furan-2-one (compound prepared in Example 25-(1 )). The yield was 95%. 1H-NMR (300MHz1 CD3OD as potassium salt): 0.59 (t, 6H), 1.00 (t, 6H)1 1.52-1.92 (m, 10H), 2.06 (q, 4H), 2.16 (s, 3H), 2.35 (s,3H), 2.38 (td, 2H), 3.91-3.98 (m, 3H), 6.78 (d, 1H), 6.85 (s, 1 H), 6.96 (d, 2H), 7.01 (s, 1 H), 7.23 (d, 1H); MS (ESI-) : 521 ([M-H]").

Example 26 Preparation of (S)-5-(4-{1 -ethyl-1 -[4-((E)-3-hydroxy-3-propyl-hex-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

o HO -== OH OH

(1) Preparation of (S)-5-(4-{1-ethyl-1-[4-((E)-3-hydroxy-3-propyl-hex-1-enyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-fur an-2-one

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1 -ethyl-1 -[4-((E)-3-hydroxy-3- propyl-hex-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 13). The yield was 70%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.98 (t, 6H), 1.54-1.74 (m, 8H), 2.02 (q, 4H), 2.14 (s, 3H), 2.26 (m, 1 H), 2.36 (s, 3H), 2.39-2.62 (m, 3H), 2.71-2.82 (m, 1 H), 4.06 (dd, 1 H), 4.14 (dd, 1 H), 4.87 (m, 1 H), 6.07 (d, 1 H), 6.75 (dd, 1H), 6.87 (d, 2H), 6.94 (s, 2H), 6.99 (td, 1H), 7.29 (d, 1H).

(2) Preparation of (S)-5-(4-{1-ethyl-1-[4-((E)-3-hydroxy-3-propyl-hex-1-enyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentano ic acid o OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1 -ethyl-1 -[4-((E)-3- hydroxy-3-propyl-hex-1-enyl)-3-methyl-phenyl]-propyl}-2-meth yl- phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 26- (1)). The yield was 93%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.62 (t, 6H), 0.95 (t, 6H), 1.39-1.51 (m, 4H), 1.56-1.62 (m, 4H), 1.87-2.02 (m,2H), 2.07 (q, 4H), 2.17 (s, 3H), 2.29 (s,3H), 2.39 (td, 2H), 3.93 (d, 2H), 3.98 (m, 1 H), 6.07 (d, 1 H), 6.75 (dd, 1 H), 6.87 (d, 2H), 6.94 (s, 2H), 6.99 (td, 1 H), 7.29 (d, 1 H); MS (ESI- ) : 523 ([M-H]-).

Example 27 Preparation of 5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentan oic acid

o

OH

(1 ) Preparation of (S )-5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-fur an-2-one

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1 -ethyl-1 -[4-(3-hydroxy-4 ,4- dimethyl-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phen ol (compound prepared in Example 3). The yield was 38%. 1H-NMR (300MHz, CDCI3): 0.58 (t, 6H), 1.06 (s, 9H), 1.76 (d, 1 H), 2.04 (q, 4H), 2.14 (s, 3H), 2.38 (s, 3H), 2.25-2.62 (m, 3H), 2.71-2.83 (m, 1H), 4.06 (dd, 1 H), 4.16 (dd, 1 H), 4.25 (d, 1 H), 4.84-4.91 (m, 1 H), 6.66 (d, 1 H), 6.87- 6.98 (m, 4H), 7.28 (d, 1 H); MS (ESI+) : 499 ([M+Na∏.

(2) Preparation of 5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentan oic acid

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S )-5-(4-{1-ethyl-1-[4-(3-hyd roxy- 4,4-dimethyl-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl- phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 27- (1)). The yield was 43%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.62 (t, 6H), 1.08 (s, 9H), 1.80-2.03 (m, 2H), 2.10 (q, 4H), 2.18 (s, 3H)1 2.38-2.42 (m, 5H), 3.92-4.03 (m, 3H), 4.22 (s, 1 H), 6.80 (d, 1 H), 6.87 (1 H, m), 6.95-7.03 (m, 3H), 7.28 (d, 1 H); MS (ESI+) : 517 ([M+Na∏.

Example 28 Preparation of 5-(4-{1 -ethyl-1-[4-((E)-3-hydroxy-4,4-dimethyl-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentan oic acid

HOOC OH (1 ) Preparation of (S)-5-(4-{1 -ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1- enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2-one HO

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1-ethyl-1-[4-((E)-3-hydroxy-4,4- dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phen ol (compound prepared in Example 14). The yield was 78%. 1H-NMR (CDCI3): 0.60 (t, 6H), 0.96 (s, 9H), 2.04 (q, 4H), 2.15 (s, 3H), 2.29 (s, 3H), 2.30-2.61 (m, 3H), 2.70-2.82 (m, 1 H), 2.92 (d, 1 H), 4.03-4.18 (m, 2H), 4.83-4.90 (m, 1 H), 6.12 (dd, 1 H), 6.66 (d, 1 H), 6.91-6.97 (m, 5H), 7.30 (d, 1 H); MS (ESI+) : 496 ([M+NH4]+).

(2) Preparation of 5-(4-{1-ethyl-1-[4-((E)-3-hydroxy-4,4-dimethyl-pent-1- enyl)-3-methyl-phenyl]-propyl}-2-methy|-phenoxy)-4(S)-hydrox y-pentanoic acid

HOO> OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1-ethyl-1-[4-((E)-3- hydroxy-4,4-dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2 -methyl- phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 28- (1 )). The yield was 41%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.60 (t, 6H), 0.96 (s, 9H), 1.88-1.97 (m, 2H), 2.05 (q, 4H), 2.17 (s, 3H), 2.29 (s, 3H), 2.62 (t, 2H), 3.82- 3.99 (m, 2H), 4.03-4.11 (m, 1 H), 4.13-4.18 (m, 1 H), 4.42-4.49 (m, 1 H), 6.12 (dd, 1 H), 6.66 (d,1 H), 6.73 (d, 1 H), 6.90-6.96 (m, 4H), 7.30 (d, 1 H); MS (ESI- ) : 495 ([M-H]-).

Example 29 Preparation of 5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

O

OH (1 ) Preparation of (S)-5-(4-{1-ethyl-1-[4-(3-hydroxy-4 ,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

HO OH

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 18). The yield was 88%. 1H-NMR (300MHz, CD3OD): 0.59 (t, 6H), 0.88 (s, 9H), 1.38-1.52 (m, 1H), 1.72-2.02 (m, 3H)1 2.09 (q, 4H), 2.15 (s, 3H), 2.25 (s,3H), 2.42 (td, 2H), 2.48- 2.59 (m, 1 H), 2.87 (m, 1 H), 3.18 (dd, 1 H), 3.90-3.99 (m, 3H), 4.02-4.19 (m, 2H), 4.90 (m, 1 H), 6.75 (d, 1 H), 6.86-6.98(m, 4H), 7.02 (d, 1 H).

(2) Preparation of 5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4 ,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentan oic acid

"HO-^^V^Ό OH OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1 -ethyl-1 -[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)- dihydro-furan-2-one (compound prepared in Example 29-(1)). The yield was 76%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.59 (t, 6H), 0.88 (s, 9H), 1.56 (m, 1 H), 1.72-2.05 (m, 3H), 2.09 (q, 4H), 2.15 (s, 3H), 2.25 (s,3H), 2.37- 2.43 (td, 2H), 2.54-2.57 (m, 1H), 2.83-2.89 (m, 1H), 3.20 (dd, 1H), 3.90-3.97 (m, 3H), 6.75 (d, 1 H), 6.86-6.97 (m, 4H), 7.02 (d, 1 H); MS (ESI-) : 497 ([M- H]-).

Example30 (S)-5-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydro xy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-4-hydroxy- pentanoic acid

O

OH (1 ) Preparation of 4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluorornethyl-but-1-enyl)-phenyl]-propyl }-2-methyl- phenol

XF3 F3C "OMOM To a solution of 4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 9) (400 mg, 0.87 mmol) in DMF (5 ml) was added NaH (34.8 mg, 0.87 mmol) and the mixture was stirred at 25 degrees C for 0.5 h. To the reaction mixture, methoxymethyl chloride (0.132 ml, 1.74 mmol) was added and stirred at 50 degrees C for overnight. The mixture was cooled to 0 degrees C, saturated NH4CI was added and extracted with diethyl ether. The organic layer was washed with brine, dried over Na2SO4, concentrated in vacuo, and chromatographed on silica gel (AcOEt/hexane/dichloromethane =1/1/10) to give the title compound (180 mg. 41 %). 1H NMR (CDCI3): 7.36 (s, 1 H), 7.33 (d, 1 H), 7.00 (d, 1 H), 6.99 (s, 1 H), 6.91- 6.84 (m, 2H), 6.65 (d, 1 H), 6.07 (d, 1 H), 4.96 (s, 2H), 4.61 (s, 1 H), 3.50 (s, 3H), 2.82-2.24 (m, 4H), 2.32 (s, 3H), 2.19 (s, 3H), 2.09 (q, 4H), 0.60 (t, 6H).

(2) Preparation of (S)-5-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one

CF3 CF3 - F3C "OMOM F3C 'OMOM

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1-ethyl-1-[3-methyl-4-((E)- 4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-eny l)-phenyl]- propyl}-2-methyl-phenol (compound prepared in Example 30-(1)). The yield was 62%. 1H-NMR (CDCI3): 7.36 (s,1 H), 7.33 (d, 1 H), 7.01-6.90 (m, 4H), 6.67 (d, 1 H), 6.05 (d, 1 H), 4.96 (s, 2H), 4.90-4.84 (m, 1 H), 4.19-4.04 (m, 2H), 3.50 (s, 3H), 2.82-2.24 (m, 4H), 2.32 (s, 3H), 2.19 (s, 3H), 2.04 (q, 4H), 0.60 (t, 6H).

(3) Preparation of (S)-5-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)-4- hydroxy-pentanoic acid

.CF3 F3C "OMOM To a solution of (S)-5-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-m8thyl- phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 30- (2)) (134 mg, 0.22 mmol) in 1 ,4-dioxane(5 ml) was added conc-HCI (0.5 ml) and the mixture was stirred at room temperature for 13 h. The reaction mixture was poured into H2O and extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO^, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (AcOEt/hexane/ dichloromethane =1/1/10) to give the title compound (85 mg, 69%) . 1H-NMR (CDCI3): 7.39-7.26 (m, 2H), 7.01-6.90 (m, 4H), 6.67 (d, 1 H), 6.07 (d, 1H), 4.90-4.84 (m, 1 H), 4.19-4.04 (m, 2H), 3.22 (s, 1H), 2.82-2.24 (m, 4H), 2.32 (s, 3H), 2.19 (s, 3H), 2.04 (q, 4H), 0.60 (t, 6H).

(4) Preparation of (S)-5-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)-4- hydroxy-pentanoic acid

Using the same procedure as described forthe preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1-ethyl-1-[3-methyl-4- ((E)-4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but- 1-enyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 35-(3)). The yield was 49%. 1H-NMR (CD3OD as potassium salt): 7.43 (d, 1 H), 7.34 (d, 1H), 6.99-6.87 (m, 4H), 6.69 (d, 1H), 6.23 (d, 1H), 4.00-3.91 (m, 3H)1 2.41-1.81 (m, 14H), 0.60 (t, 6H).; MS (ESI-):575 ([M-H]").

Example 31 Preparation of (S)-5-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-h ydroxy-pentanoic acid

HOOC OH (1) Preparation of (S)-5-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3 - trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-phenoxymethy l)-dihydro- furan-2-one

F3C' OH

To a solution of (S)-5-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl- phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 30- (3)) (45 mg, 0.08 mmol) in MeOH (5 ml) was added palladium hydroxide (4.5 mg 10%w/w)) at room temperature under H2 gas and the mixture was stirred for 3 h. The reaction mixture was filtered through celite and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (Hexane/C^CV EtOAc=I :1 : 1 )to give the title compound (45 mg, quant). 1H-NMR (CDCI3); 7.01-6.80 (m, 5H), 6.70 (d, 1 H), 4.90-4.84 (m, 1 H), 4.19- 4.04 (m, 2H)1 2.88-1.90 (m, 18H), 0.60 (t, 6H).

(2) Preparation of (S)-5-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-h ydroxy-pentanoic acid

HOOC. F3C' OH Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1-ethyl-1-[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-butyl)-phenyl]- propyl}-2-methyl- phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 31- (1 )). The yield was 54%. 1H-NMR (300MHz, CD3OD as potassium salt): 7.05-6.88 (m, 5H), 6.80 (d, 1 H), 4.01-3.92 (m, 3H), 2.87-2.77 (m, 4H), 2.44-1.81 (m, 14H), 0.60 (t, 6H); MS (ESI-) : 577 ([M-H]").

Example 32 Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(1 -hydroxy-cyclobutylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

o HO OH OH

(1 ) Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(1-hydroxy-cyclobutylethynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

OH OH

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1 -ethyl-1 -[4-(1-hydroxy- cyclobutylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 6). The yield was 51 %. 1H-NMR (300MHz, CDCI3): 0.58 (t, 6H), 1.64-1.90 (m, 4H), 2.02 (q, 4H), 2.14 (s, 3H), 2.26 (m, 2H), 2.34 (s, 3H), 2.39-2.62 (m, 3H), 2.71-2.82 (m, 1 H), 4.06 (dd, 1 H), 4.14 (dd, 1 H), 4.87 (m, 1 H), 6.68 (d, 1 H), 6.84 (m, 2H), 6.91 (d, 1 H), 7.00 (S1 1 H), 7.27 (d, 1 H). (2) Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(1-hydroxy-cyclobutylethynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

o OH OH OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1 -ethyl-1 -[4-(1-hydroxy- cyclobutylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy methyl)- dihydro-furan-2-one (compound prepared in Example 32-(1)). The yield was 95%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.62 (t, 6H), 1.79-2.01 (m,4H), 2.06 (q, 4H), 2.20 (s,3H), 2.25 (m, 4H), 2.32 (s, 3H), 2.39 (td, 2H), 3.89-3.98 (m, 3H), 6.73 (d, 1 H), 6.80 (m, 2H), 6.91 (d, 2H), 6.96 (s, 1 H), 7.20 (d, 1 H); MS (ESI-) : 477 ([M-H∏.

Example 33 Preparation of (S)-5-[4-(1 -ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclobutyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentanoic acid

o

OH

(1 ) Preparation of (S)-5-[4-(1 -ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclobutyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dihydro-furan -2-one

OH OH

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-(1 -ethyl-1 -{4-[(E)-2-(1-hydroxy- cyclobutyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenol (compound prepared in Example 15). The yield was 74%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.64-1.90 (m, 4H), 2.04 (q, 4H), 2.15 (s, 3H), 2.26 (m, 2H), 2.34 (s, 3H), 2.39-2.62 (m, 3H), 2.71-2.82 (m, 1 H), 4.06 (dd, 1 H), 4.14 (dd, 1 H), 4.84-4.91 (m, 1 H), 6.34 (d, 1 H), 6.66 (d, 1 H), 6.81 (d, 1 H), 6.91-6.97 (m, 4H), 7.40 (d, 1 H).

(2) Preparation of (S)-5-[4-(1 -ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclobutyl)-vinyl]- 3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentano ic acid

o

OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-[4-(1 -ethyl-1 -{4-[(E)-2-(1- hydroxy-cyclobutyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methyl - phenoxymethyl]-dihydro-furan-2-one (compound prepared in Example 33- (1)). The yield was 98%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.59 (t, 6H), 1.52-1.82 (m, 4H), 1.83-1.92 (m, 1 H), 1.87-2.10 (m,2H), 1.97 (q, 4H), 2.06 (s, 3H), 2.19 (s, 3H), 2.15 (m, 4 H), 2.31 (td, 2H), 3.81-3.89 (m, 3H), 6.25 (d, 1 H), 6.67-6.77 (m, 3H), ), 6.84-6.88 (m, 3H), 7.25 (d, 1 H) ; MS (ESI-) : 479 ([M-H]').

Example 34 Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(1 -hydroxy-cyclopentylethynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

O

OH

(1 ) Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(1-hydroxy-cyclopentylethynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one Using the same procedure as described for the preparation of Example 1-( (6), the title compound was prepared from 4-{1-ethyl-1-[4-(1-hydroxy- cyclopentylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 7). The yield was 58%. 1H-NMR (300MHz, CDCI3): 0.58 (t, 6H), 1.75-1.95 (m, 5H), 1.97-2.10 (m, 8H), 2.14 (s, 3H), 2.27-2.35 (m, 1 H), 2.36 (s, 3H), 2.39-2.62 (m, 2H), 2.71- 2.82 (m, 1 H), 4.06 (dd, 1 H), 4.14 (dd, 1 H), 4.84-4.91 (m, 1 H), 6.66 (d, 1 H), 6.85 (s, 1H), 6.94 (d, 2H), 6.90 (s, 1 H), 7.26 (d, 1H) ; MS(ESI+) : 497 ([M+Na]+).

(2) Preparation of (S)-5-(4-{1-ethyl-1-[4-(1-hydroxy-cyclopentylethynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

o OH HO ^^Ϊ^O' OH OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1-ethyl-1-[4-(1-hydroxy- cyclopentylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenox ymethyl)- dihydro-furan-2-one (compound prepared in Example 34-(1 )). The yield was 83%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.60 (t, 6H), 1.81-1.85 (m, 5H), 1.91-2.01 (m, 5H), 2.02 (q, 4H), 2.16 (s, 3H), 2.34 (s,3H), 2.39 (td, 2H), 3.90-3.99 (m, 3H), 6.78 (d, 1 H), 6.84 (s, 1H), 6.94 (dd, 2H), 7.00 (s, 1H), 7.22 (d, 1 H); MS (ESI-) : 491 ([M-H]").

Example 35 Preparation of (S)-5-[4-(1 -ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentanoic acid O

OH

(1 ) Preparation of (S)-5-[4-(1-ethyl-1-{4-[(E)-2-(1-hydroxy-cyclopentyl)-vinyl] - 3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dihydro-fur an-2-one

HO =. OH OH

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-(1-ethyl-1-{4-[(E)-2-(1-hydroxy- cyclopentyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenol (compound prepared in Example 10). The yield was 54%. 1H-NMR (300MHz, CDCI3): 0.58 (t, 6H), 1.75-1.95 (m, 5H), 1.97-2.10 (m, 8H)1 2.14 (S1 3H), 2.34 (s,3H), 2.38 (m, 1 H), 2.39-2.62 (m, 2H), 2.71-2.82 (m, 1 H), 4.06 (dd, 1 H), 4.14 (dd, 1 H), 4.84-4.91 (m, 1 H), 6.23 (d, 1 H), 6.68 (d, 1H), 6.81 (d, 1H), 6.90-6.99 (m, 4H), 7.32 (d, 1H); MS (ESI+) : 499 ([M+Na∏.

(2) Preparation of (S)-5-[4-(1-ethyl-1-{4-[(E)-2-(1-hydroxy-cyclopentyl)-vinyl] - 3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentano ic acid

O r^o OH OH OH O <y~° Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-[4-(1-ethyl-1-{4-[(E)-2-(1- hydroxy-cyclopentyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methy l- phenoxymethyl]-dihydro-furan-2-one (compound prepared in Example 35- (1)). The yield was 97%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.60 (t, 6H), 1.76-2.00 (m, 12H), 2.06 (q, 4H), 2.16 (s, 3H), 2.29 (s,3H), 2.41 (td, 2H), 3.90-3.99 (m, 3H), 6.23 (d, 1 H), 6.77 (d,1 H), 6.84 (d, 1 H), 6.93-6.99 (m, 4H), 7.32 (d, 1 H); MS (ESI-) : 493 ([M-H∏.

Example 36 Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(1 -hydroxy-cyclohexylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

O

OH

(1) Preparation of (S)-5-(4-{1-ethyl-1-[4-(1-hydroxy-cyclohexylethynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

OH OH

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1 -ethyl-1 -[4-(1-hydroxy- cyclohexylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 8). The yield was 72%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.61-1.79 (m, 6H), 1.99-2.09 (m, 8H), 2.14 (s, 3H), 2.26 (m, 1 H), 2.38 (s, 3H), 2.39-2.62 (m, 3H), 2.71-2.82 (m, 1 H), 4.08 (dd, 1 H), 4.14 (dd, 1 H), 4.84-4.91 (m, 1 H), 6.65 (d, 1 H), 6.87 (s, 1 H), 6.92 (d, 2H), 7.00 (s, 1 H), 7.27 (d, 1 H).

(2) Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(1-hydroxy-cyclohexylethynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid o cr° OH OH HO A^v^o OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1 -ethyl-1 -[4-(1-hydroxy- cyclohexylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy methyl)- dihydro-furan-2-one (compound prepared in Example 36-(1)). The yield was 92%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.59 (t, 6H), 1.59-1.89 (m, 9H), 1.95-2.03 (m, 3H), 2.08 (q, 4H), 2.15 (s, 3H), 2.35 (s,3H), 2.36 (td, 2H), 3.89-3.98 (m, 3H), 6.77 (d, 1 H), 6.84 (s, 1 H), 6.95 (d, 1 H), 7.00 (s, 1H), 7.23 (d, 1 H); MS (ESI-) : 505 ([M-HV).

Example 37 Preparation of (S)-5-[4-(1 -ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentanoic acid

o HO Λ^γ^0 — OH OH

(1 ) Preparation of (S)-5-[4-(1 -ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclohexyl)-vinyl]- 3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dihydro-fur an-2-one

OH

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-(1 -ethyl-1 -{4-[(E)-2-(1-hydroxy- cyclohexyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenol (compound prepared in Example 11). The yield was 71%. 1H-NMR(300MHz, CDCI3): 0.60 (t, 6H), 1.61-1.79 (m, 6H), 1.99-2.09 (m, 8H), 2.14 (s, 3H), 2.26 (m, 1 H), 2.30 (s, 3H), 2.39-2.62 (m, 3H), 2.71-2.82 (m, 1 H), 4.08 (dd, 1 H), 4.14 (dd, 1 H), 4.84-4.91 (m, 1 H), 6.20 (d, 1 H), 6.66 (d, 1 H), 6.81 (d, 1 H), 6.89-6.97 (m, 5H), 7.32 (d, 1 H).

(2) Preparation of (S)-5-[4-(1 -ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclohexyl)-vinyl]- 3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pθntan oic acid

^^^o OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-[4-(1 -ethyl-1 -{4-[(E)-2-(1- hydroxy-cyclohexyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methyl - phenoxymethyl]-dihydro-furan-2-one (compound prepared in Example 37- (1)). The yield was 98%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.60 (t, 6H), 1.30-1.37 (m, 1H), 1.56-2.02 (m, 11 H), 2.06 (q, 4H), 2.15 (s, 3H), 2.28 (s,3H), 2.37 (td, 2H), 3.89-3.98 (m, 1 H), 6.16 (d, 1 H), 6.76-6.98 (m, 2H), 6.84 (d, 1 H), 6.93- 6.98 (m, 3H), 7.30 (d, 1 H); MS (ESI-) : 507 ([M-H∏.

Example 38 Preparation of 5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-heptyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

HOOC OH (1 ) Preparation of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-hept-6-en-1 -ynyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenol

Ή To a solution of 4-[1 -ethyl-1 -(4-ethynyl-3-methyl-phenyl)-propyl]-2-methyl- phenol (compound prepared in Example 1-(3)) (1 g, 3.42 mmol) in THF (20 ml) was added 1.6N n-BuLi in Hex (5.34 ml, 8.55 mmol) at -78 degrees C under nitrogen atmosphere. The mixture was stirred at -78 degrees C for 1 h and 2,2-dimethyl-4-pentenal (1.39 ml, 10.26 mmol) was added. The reaction mixture was warmed to room temperature and stirred for 12 h. The mixture was poured into saturated NH4CI aq. and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by Silica gel chromatography (EtOAc: n-Hexane=1 :12) to give the title compound (829 mg, 60%). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.04 (d, 6H), 2.03 (q, 4H), 2.18 (s, 3H), 2.20 (m, 2H), 2.38 (s, 3H), 4.34 (s, 1 H), 5.10 (m, 2H)1 5.87 (m, 1 H), 6.65 (d, 1 H), 6.80-7.00 (m, 4H), 7.28 (d, 1 H); MS (ESI-) : 403 ([M-H∏.

(2) Preparation of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-heptyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

OH To a solution of4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-hept-6-en-1 -ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 38- (1 )) (830 mg, 2.05 mmol) in MeOH (20 ml) was added 10% palladium on activated carbon (100 mg) and the mixture was stirred at room temperature under H2 gas for 3 h. The mixture was filtered through celite and concentrated under reduced pressure. The obtained residue was purified by flash chromatography on silica gel (n-Hexane:EtOAc=10:1 ) to give the title compound (670 mg, 80%). 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 0.85 (m, 9H), 1.21 (m, 4H), 1.52 (m, 1 H), 1.77 (m, 1 H), 2.03 (q, 4H), 2.19 (s, 3H), 2.24 (s, 3H), 2.55 (m, 1 H), 2.85 (m, 1 H), 3.32 (d, 1 H), 6.64 (d, 1 H), 6.84-7.03 (m, 5H). (3) Preparation of (S)-5-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-heptyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1-ethyl-1-[4-(3-hydroxy-4,4- dimethyl-heptyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 38-(2)). The yield was 52%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.86 (m, 9H), 1.24 (m, 4H), 1.50 (m, 1 H), 1.77 (m, 1 H), 2.03 (q, 4H), 2.15 (s, 3H), 2.25 (s, 3H), 2.29-2.62 (m, 4H), 2.71-2.89 (m, 2H), 3.30 (d, 1 H), 4.12 (m, 2H), 4.88 (m, 1 H), 6.66 (d, 1 H), 6.91 (m, 4H), 7.02 (cl, 1 H).

(4) Preparation of 5-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-heptyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentan oic acid

HOOC ■σ OH OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1 -ethyl- 1-[4-(3-hydroxy- 4,4-dimethyl-heptyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)- dihydro-furan-2-one (compound prepared in Example 38-(3)). The yield was 90%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.59 (t, 6H), 0.82 (m, 9H), 1.21 (m, 4H), 1.50 (m, 1 H), 1.70 (m, 1 H), 1.89 (m, 2H), 2.05 (q, 4H), 2.14 (s, 3H), 2.24 (s, 3H), 2.37 (t, 2H), 2.54 (m, 1 H), 2.86 (m, 1 H), 3.22 (d, 1H), 3.94 (m, 3H), 6.76 (d, 1 H), 6.92 (m, 4H), 7.01 (d, 1 H); MS (ESI-) : 525 ([M-H]").

Example 39 Preps^JFTi of 5-(4-{1 -ethyl-1 -μ-β-hydroxy^-dimethyl-octyiy-S-methyl- pheriyi]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

HOOC OH (1 ) Preparation of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-oct-1 -ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol

HO

Using the same procedure as described for the preparation of Example 38- (1), the title compound was prepared from 4-[1-ethyl-1-(4-ethynyl-3-methyl- phenyl)-propyl]-2-methyl-phenol (compound prepared in Example 1-(3)) and 2,2-dimethyl hexanal. The yield was 24%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.91 (t, 3H), 1.01 (s,3H), 1.03 (s, 3H), 1.30 (m, 6H), 2.03 (q, 4H), 2.19 (s, 3H), 2.38 (s, 3H), 4.33 (m, 1H), 6.65 (d, 1 H), 6.83-7.00 (m, 4H)1 7.29 (d, 1H).

(2) Preparation of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-octyl)-3-methyl- phenyl]-propyl}-2-methyl- phenol

HO" H

Using the same procedure as described for the preparation of Example 38- (2), the title compound was prepared from 4-{1 -ethyl-1 -[4-(3-hydroxy-4 ,4- dimethyl-oct-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno l (compound prepared in Example 39-(1 )). The yield was 86%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 0.86 (m, 9H), 1.26 (m, 6H), 1.52 (m, 1H), 1.78 (m, 1 H), 2.03 (q, 4H), 2.20 (s, 3H)1 2.25 (s, 3H), 2.55 (m, 1 H), 2.85 (m, 1 H)1 3.32 (m, 1H)1 6.64 (d, 1H)1 6.84-6.92 (m, 4H), 7.02 (d, 1 H).

(3) Preparation of (S)-5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-octyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

OH

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1-ethyl-1-[4-(3-hydroxy-4,4- dimethyl-octyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 39-(2)). The yield was 58%. 1H-NMR (300MHz1 CDCI3): 0.59 (t, 6H)1 0.85 (m, 9H)1 1.23 (m, 6H)1 1.52 (m, 1 H)1 1.76 (m, 1 H), 2.03 (q, 4H)1 2.15 (s, 3H), 2.25 (s, 3H)1 2.29-2.62 (m, 4H)1 2.71-2.88 (m, 2H)1 3.31 (d, 1H)1 4.11 (m, 2H)1 4.87 (m, 1H), 6.66 (d, 1H)1 6.92 (m, 4H)1 7.02 (d, 1 H).

(4) Preparation of 5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-octyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

HOOC. OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1 -ethyl-1 -[4-(3-hydroxy~ 4,4-dimethyl-octyl)-3-methyl-phenyl]-propyl}-2-methyl-phenox ymethyl)- dihydro-furan-2-one (compound prepared in Example 39-(3)). The yield was 92%. 1H-NMR (300MHz1 CD3OD as potassium salt): 0.59 (t, 6H), 0.84 (m, 9H), 1.25 (m, 6H), 1.51 (m, 1H), 1.73 (m, 1 H)1 1.89 (m, 2H)1 2.05 (q, 4H)1 2.15 (s, 3H), 2.24 (s, 3H), 2.37 (t, 2H), 2.55 (m, 1 H), 2.86 (m, 1 H), 3.23 (d, 1H), 3.94 (m, 3H), 6.76 (d, 1 H), 6.92 (m, 4H), 7.02 (d, 1 H); MS (ESI-) : 539 ([M-H]").

Example 40 Preparation of 5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-decyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

O

OH (1) Preparation of 2,2-dimethyl-octanoic acid ethyl ester O OEt OEt

To a solution of lsobutyric acid ethyl ester (4.3 g, 37.02 mmol) in anhydrous THF (37 ml) under nitrogen atmosphere at -78 degrees C was added LDA (6.7 ml, 10.65 mmol) and the mixture was stirred for 30 min. To the mixture, iodohexane (6 ml, 40.72 mmol.) was added and the mixture was stirred at - 78 degrees C for 5 h. Then the mixture was warmed to room temperature and poured into 1 N-HCI and the products were extracted with diethyl ether. The extracts were washed with brine, dried over MgSO4, filtered, and concentration in vacuo. The obtained residue was purified by distillation (78-82 degrees C, 12 torr) to give the title compound (6.5 g, 87%). 1H-NMR (300MHz, CDCI3): 0.87 (t, 3H), 1.15 (s, 6H), 1.21-1.40 (m, 10H), 1.50 (m, 2H), 4.10 (q, 2H).

(2) Preparation of 2,2-dimethyl-octan-1-ol O OEt

To a solution of 2,2-dimethyl-octanoic acid ethyl ester (compound prepared in Example 40-(1 )) (5.79 g, 28.90 mmol) in anhydrous THF (29 ml) at 0 degrees C under nitrogen atmosphere was added 1 N-LiAIH4ZTHF (14.5 ml, 14.50 mmol) and the mixture was stirred at O degrees C for 4 h. Then the mixture was warmed to room temperature and quenched with H20, 10% NaOH solution and H2O. The reaction mixture was filtered through celite and the filtrate was washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. The obtained residue was purified by silica gel chromatography eluting with dichloromethane to give the title compound (3.12 g, 69.0 %) . 1H-NMR(300MHz, CDCI3): 0.86(s, 6H), 0.88(t, 3HJ, 1.25 (m, 1 H), 3.31(s, 2H).

(3) Preparation of 2,2-dimethyl-octanal

"OH

To a solution of 2,2-dimethyl-octan-1-ol (compound prepared in Example 40-(2)) (3.12 g, 19.71 mmol) in anhydrous dichloromethane (27.5 ml) under nitrogen atmosphere was added PCC (6.54 g, 30.35 mmol) and the mixture was stirred at room temperature for 3 h. The mixture was diluted with diethyl ether and filtered through a celite and silicagel and concentrated in vacuo. The obtained residue was purified by silica gel chromatography (hexane/ EtOAc= 10:1)to give the title compound (2.55 g, 82%) . 1H-NMR (300MHz, CDCI3): 0.88 (t, 3H), 1.04 (s, 6H), 1.15-1.29 (m, 9H), 1.43-1.48 (m, 2H), 9.21 (s, 1 H).

(4) Preparation of 4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-dec-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol

OH

Using the same procedure as described for the preparation of Example 38- (1), the title compound was prepared from 4-[1 -ethyl- 1-(4-ethynyl-3-methyl- phenyl)-propyl]-2-methyl-phenol (compound prepared in Example 1-(3)) and 2,2-dimethyl-octanal (compound prepared in Example 40-(3)). The yield was 58%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.88 (t, 3H), 1.01 (s,3H), 1.02 (s, 3H), 1.25-1.49 (m, 10H), 1.75 (d, 1 H), 2.02 (q, 4H), 2.19 (s, 3H), 2.38 (s, 3H), 4.32 (d, 1 H), 4.52 (s, 1 H). 6.65 (d, 1 H), 6.82-6.86 (m, 2H), 6.93 (dd, 1 H), 7.00 (s, 1 H), 7.28 (d, 1 H).

(5) Preparation of 4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-decyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

OH

Using the same procedure as described for the preparation of Example 38- (2), the title compound was prepared from 4-{1-ethyl-1-[4-(3-hydroxy-4,4- dimethyl-dec-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno l (compound prepared in Example 40-(4)). The yield was 81%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.86 (t, 9H), 1.17-1.29 (m, 9H), 1.42-1.60 (m, 2H), 1.72-1.83 (m, 1 H), 2.03 (q, 4H), 2.19 (s, 3H), 2.24 (s, 3H), 2.50-2.60 (m, 1 H), 2.82-2.91 (m, 1 H), 3.34 (d, 1 H), 5.01 (s, 1 H), 6.64 (d, 1 H), 6.84 (dd, 1 H), 6.90-6.92 (m, 2H), 7.02 (s, 1 H), 7.26 (d, 1 H).

(6) Preparation of (S)-5-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-decyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

OH

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1-ethyl-1-[4-(3-hydroxy-4,4- dimethyl-decyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 40-(5)). The yield was 67%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.83 (s, 3H), 0.85 (s, 3H), 0.88 (t, 3H), 1.25-1.49 (m, 11 H), 1.40-1.52 (m, 1 H), 1.78 (m, 1 H), 2.03 (q, 4H), 2.15 (s, 3H), 2.25 (s, 3H), 2.29-2.62 (m, 4H), 2.71-2.88 (m, 2H), 3.30 (d, 1 H), 4.04-4.19 (m, 2H), 4.87 (m, 1 H), 6.66 (d, 1 H), 6.92 (m, 4H), 7.02 (d, 1 H); MS (ESI+) : 573 ([M+Na]+).

(7) Preparation of 5-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-decyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid HO' OH Λ~"Υ OH^O'

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1-ethyl-1-[4-(3-hydroxy- 4,4-dimethyl-decyl)-3-methyl-phenyl]-propyl}-2-methyl-phenox ymethyl)- dihydro-furan-2-one (compound prepared in Example 40-(6)). The yield was 95%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.58 (t, 6H), 0.80 (s, 3H), 0.84 (s, 3H), 0.89 (t, 3H), 1.16-1.33 (m, 10H), 1.46-1.52 (m, 1 H), 1.68-2.00 (m, 4H), 2.05 (q, 4H), 2.14 (s, 3H), 2.24 (s,3H), 2.37-2.40 (td, 2H), 2.55-2.57 (m, 1 H), 2.84-2.85 (m, 1 H), 3.23 (d, 1 H), 3.88-4.01 (m, 3H), 6.75 (d, 1 H), 6.84 (s, 1 H), 6.84-6.95 (m, 3H), 7.01 (d, 1 H); MS (ESI+) : 591 ([M+Na]+).

Example 41 Preparation of 5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-nonyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

o

OH (1 ) Preparation of 2,2-dimethyl-heptanoic acid ethyl ester O O OEt OEt

Using the same procedure as described for the preparation of Example 40- (1 ), the title compound was prepared from lsobutyric acid ethyl ester and iodopentane. The yield was 86%. 1H-NMR (300MHz, CDCI3): 0.87 (t, 3H), 1.16 (s, 6H), 1.21-1.40 (m, 8H), 1.54 (m, 2H), 4.14 (q, 2H). (2) Preparation of 2,2-dimethyl-heptan-1-ol O OEt

Using the same procedure as described for the preparation of Example 40- (2), the title compound was prepared from 2,2-dimethyl-heptanoic acid ethyl ester (compound prepared in Example 41 -(1 )). The yield was 89%. 1H-NMR (300MHz, CDCI3): 0.86 (s, 6H), 0.89 (t, 3H), 1.23-1.35 (m, 9H), 3.31 (s, 2H).

(3) Preparation of 2,2-dimethyl-heptanal

Using the same procedure as described for the preparation of Example 40- (3), the title compound was prepared from 2,2-dimethyl-heptan-1-ol (compound prepared in Example 41 -(2)). The yield was 83%. 1H-NMR (300MHz, CDCI3): 0.88 (t, 3H), 1.05 (s, 6H), 1.20-1.31 (m, 6H), 1.42-1.48 (m, 2H), 9.45 (s, 1 H).

(4) Preparation of 4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-non-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol

HO OH Using the same procedure as described for the preparation of Example 38- (1), the title compound was prepared from 4-[1 -ethyl- 1-(4-ethy nyl-3-methyl- phenyl)-propyl]-2-methyl-phenol (compound prepared in Example 1-(3)) and 2,2-dimethyl-heptanal (compound prepared in Example 41 -(3)). The yield was 80%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.86 (t, 3H), 1.01 (s,3H), 1.03 (s, 3H), 1.25-1.49 (m, 8H), 1.75 (m, 1 H), 2.02 (q, 4H), 2.19 (s, 3H), 2.38 (s, 3H), 4.33 (d, 1 H), 4.60 (s, 1 H). 6.65 (d, 1 H), 6.86 (dd, 2H), 6.94 (dd, 1 H), 7.01 (s, 1 H), 7.27 (d, 1 H).

(5) Preparation of 4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-nonyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

Using the same procedure as described for the preparation of Example 38- (2), the title compound was prepared from 4-{1-ethyl-1-[4-(3-hydroxy-4,4- dimethyl-non-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno l (compound prepared in Example 41 -(4)). The yield was 81%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.86 (t, 9H), 1.17-1.29 (m, 9H), 1.42-1.60 (m, 2H), 1.72-1.83 (m, 1 H), 2.03 (q, 4H), 2.19 (s, 3H), 2.24 (s, 3H), 2.50-2.55 (m, 1 H), 2.82-2.91 (m, 1 H), 3.34 (dd, 1 H), 5.01 (s, 1 H), 6.64 (d, 1 H), 6.84 (dd, 2H), 6.90-6.92 (m, 3H), 7.01 (s, 1 H), 7.27 (d, 1 H).

(6) Preparation of (S)-5-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-nonyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

OH

Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1-ethyl-1-[4-(3-hydroxy-4,4- dimethyl-nonyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 41 -(5)). The yield was 65%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.83 (s, 3H), 0.85 (s, 3H), 0.87 (t, 3H), 1.15-1.33 (m, 10H), 1.42-1.54 (m, 1H), 1.71-1.83 (m, 1H), 2.03 (q, 4H), 2.15 (s, 3H), 2.25 (s, 3H), 2.29-2.61 (m, 4H), 2.71-2.88 (m, 2H), 3.30 (d, 1 H), 4.11 (m, 2H), 4.87 (m, 1 H), 6.65 (d, 1 H), 6.89-6.97 (m, 4H), 7.02 (d, 1 H). (7) Preparation of 5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4 ,4-dimethyl-nonyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

HO .A' v^ OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-5-(4-{1 -ethyl-1 -[4-(3-hydroxy- 4,4-dimethyl-nonyl)-3-methyl-phenyl]-propyl}-2-methyl-phenox ymethyl)- dihydro-furan-2-one (compound prepared in Example 41 -(6)). The yield was 92%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.58 (t, 6H), 0.80 (s, 3H)1 0.84 (s, 3H), 0.89 (t, 3H), 1.16-1.33 (m, 8H), 1.46-1.52 (m, 1 H), 1.65-2.00 (m, 3H), 2.05 (q, 4H), 2.14 (s, 3H), 2.24 (s,3H), 2.37-2.40 (td, 2H), 2.55-2.57 (m, 1 H), 2.84-2.85 (m, 1 H), 3.23 (d, 1 H), 3.90-3.91 (m, 3H), 6.75 (d, 1 H), 6.84 (s, 1 H), 6.84-6.97 (m, 3H), 7.01 (d, 1 H); MS (ESI-) : 553 ([M-H]").

Example 42 Preparation of (R)-5-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

ΛN\> o o

Preparation of (R)-5-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

Ci .Λ>> O ^-0 O Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy- pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(4)) and Toluene-4-sulfonic acid (R)-5-oxo-tetrahydro-furan-2- yl methyl ester. The yield was 51%. 1H-NMR (300MHz, CDCI3): 0.58 (t, 6H), 1.11 (t, 6H), 1.76 (q, 4H), 2.02 (q, 4H), 2.14 (s, 3H), 2.36 (s, 3H), 2.22-2.61 (m, 3H), 2.71-2.83 (m, 1H), 4.06 (dd, 1 H), 4.14 (dd, 1 H), 4.87 (m, 1 H), 6.65 (d, 1 H), 6.87 (s, 1 H), 6.92 (d, 2H), 6.98 (s, 1 H)1 7.27 (d, 1H); MS (ESI+) : 499 ([M+Na]+).

Example 43 Preparation of 5-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid

o

Preparation of 5-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid

O .ΛVV O Po OH Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (R)-5-(4-{1 -ethyl- 1-[4-(3-ethyl-3- hydroxy-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)- dihydro-furan-2-one (compound prepared in Example 42). The yield was 98%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.61 (t, 6H)1 1.11 (t, 6H), 1.70-1.77 (m, 5H), 1.90-2.01 (m, 1H), 2.07 (q, 4H), 2.17 (s, 3H), 2.36 (s, 3H), 2.37 (td, 2H), 3.91-4.00 (m, 3H), 6.79 (d, 1H), 6.85 (s, 1H), 6.95 (d, 2H), 7.01 (s, 1 H), 7.24 (d, 1H); MS (ESI-) : 493 ([M-H]"). Example 44 Preparation of (R)-5-(4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

ΛW,

O P OH Preparation of (R)-5-(4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

HO A' A\V O OH O OH Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1 -ethyl-1-[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno l (compound prepared in Example 1-(5)) and toluene-4-sulfonic acid (R)-5-oxo-tetrahydro- furan-2-ylmethyl ester. The yield was 82%. 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 0.92 (t, 6H), 1.64 (q, 4H), 2.06 (q, 4H), 2.16 (s, 3H), 2.31 (s, 3H), 2.34-2.62 (m, 3H)1 2.72-2.83 (m, 1 H), 4.06 (dd, 1 H), 4.15 (dd, 1 H), 4.87 (m, 1 H), 6.01 (d, 1 H), 6.66 (d, 1 H), 6.74 (d, 1 H), 6.91-6.98 (m, 4H), 7.29 (d, 1 H); MS (ESI+) : 501 ([M+Na]+).

Example 45 Preparation of 5-(4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentan oic acid

o HO

Preparation of 5-(4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentan oic acid Λ\N o P OH Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (R)-5-(4-{1-ethyl-1-[4-((E)-3-ethyl- 3-hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phe noxymethyl)- dihydro-furan-2-one (compound prepared in Example 44). The yield was 91%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.60 (t, 6H), 0.92 (t, 6H), 1.63 (q, 4H), 1.81-2.01 (m, 3H), 2.06 (q, 4H), 2.16 (s, 3H), 2.28 (s, 3H), 2.38 (td, 2H), 3.89-3.99 (m, 3H), 6.01 (d, 1H), 6.74 (d, 1 H), 6.79 (s, 1 H), 6.86 (s, 1H), 6.93-6.95 (m, 3H), 7.29 (d, 1 H); MS (ESI-) : 495 ([M-H]").

Example 46 Preparation of (R)-5-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)-dihydro- furan-2-one

Λγ^o

(1) Preparation of (R)-5-(4-{1-ethyl-1-[3-methyl-4-(4 ,4 ,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one

o_0M0M -_OMOM CF3 Uh3 Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1 -ethyl-1 -[3-methyl-4-(4 ,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenol (compound prepared in Example 2-(2)) and toluene-4-sulfonic acid (R)-5-oxo-tetrahydro-furan-2-ylmethyl ester. The yield was 42%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 2.04 (q, 4H), 2.15 (s, 3H), 2.27-2.50 (m, 2H), 2.39 (s, 3H), 2.56 (m, 1 H), 2.77 (m, 1 H), 3.48 (s, 3H), 4.12 (m, 2H), 4.88 (m, 1 H), 5.15 (s, 2H), 6.67 (d, 1 H), 6.85-7.03 (m, 4H), 7.37 (d, 1 H).

(2) Preparation of (R)-5-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-pheno xymethyl)- dihydro-furan-2-one

CF3 ,, OMOM CF3 Using the same procedure as described for the preparation of Example 2- (4), the title compound was prepared from (R)-5-(4-{1-ethyl-1-[3-methyl-4- (4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-yn yl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 46-(1)). The yield was 54%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 2.04 (q, 4H), 2.14 (s, 3H), 2.27-2.50 (m, 2H), 2.38 (s, 3H), 2.55 (m, 1 H), 2.76 (m, 1 H), 4.02 (s, 1 H), 4.12 (m, 2H), 4.88 (m, 1 H), 6.66 (d, 1 H), 6.85-7.03 (m, 4H), 7.35 (d, 1 H); MS (ESI-) : 555 ([M-H]").

Example 47 Preparation of (R)-5-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-4-hydroxy- pentanoic acid

OH Preparation of (R)-5-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-4-hydroxy- pentanoic acid

CT0 OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (R)-5-(4-{1-ethyl-1-[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 46-(2)). The yield was 96%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.59 (t, 6H), 1.80-2.00 (m, 2H), 2.07 (q, 4H), 2.15 (s, 3H), 2.35 (s, 3H), 2.38 (m, 2H), 3.94 (m, 3H), 6.78 (d, 1 H), 6.84 (m, 1 H), 6.93-6.98 (m, 3H), 7.28 (d, 1H); MS (ESI-) : 573 ([M- H]-).

Example 48 Preparation of (R)-5-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xymethyl)- dihydro-furan-2-one

rr^° CF?"

(1) Preparation of (R)-5-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one

.,,.0MOM ,__0M0M CF3 Oh3 Using the same procedure as described for the preparation of Example 1- (6), the title compound was prepared from 4-{1-ethyl-1-[3-methyl-4-((E)- 4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-eny l)-phenyl]- propyl}-2-methyl-phenol (compound prepared in Example 30-(1)) and toluene-4-sulfonic acid (R)-5-oxo-tetrahydro-furan-2-ylmethyl ester. The yield was 89%. 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 2.05 (q, 4H), 2.15 (s, 3H), 2.32 (s, 3H), 2.25-2.85 (m, 4H), 3.50 (s, 3H), 4.12 (m, 2H), 4.88 (m, 1H), 4.96 (s, 2H), 6.06 (d, 1 H), 6.67 (d, 1 H), 6.96 (m, 4H), 7.34 (m, 2H).

(2) Preparation of (R)-5-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl- phenoxymethyl)-dihydro-furan-2-one

CF?H

Using the same procedure as described for the preparation of Example 2- (4), the title compound was prepared from (R)-5-(4-{1-ethyl-1-[3-methyl-4- ((E)-4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but- 1-enyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 48-(1)). The yield was 84%. 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 2.05 (q, 4H), 2.15 (s, 3H), 2.34 (s, 3H), 2.25-2.83 (m, 4H), 3.24 (s, 1H), 4.11 (m, 2H), 4.88 (m, 1H), 6.08 (d, 1H), 6.67 (d, 1H), 6.95 (m, 4H), 7.35 (m, 2H); MS (ESI-) : 557 ([M-H]").

Example 49 Preparation of 5-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-4(R)-hydroxy- pentanoic acid O

OH

Preparation of 5-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-4(R)-hydroxy- pentanoic acid

CF?H OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (R)-5-(4-{1-ethyl-1-[3-methyl-4- ((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl) -phenyl]-propyl}-2- methyl-phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 48-(2)). The yield was 93%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.60 (t, 6H), 1.80-2.20 (m, 2H), 2.07 (q, 4H), 2.15 (s, 3H), 2.32 (s, 3H), 2.37 (m, 2H)1 3.94 (m, 3H), 6.18 (d, 1H), 6.77 (d, 1H), 6.86 (m, 1H), 6.97 (m, 3H), 7.37 (m, 2H); MS (ESI-) : 575 ([M-H]").

Example 50 Preparation of 5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid

OH ' ' OH Preparation of 5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid

OH To a solution of 4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-phenyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 18) (190 mg, 0.50 mmol) in anhydrous DMF (5 ml) under nitrogen atmosphere were added K2CO3 (138.2 mg, 1.0 mmol) and (R)-toluene-4-sulfonic acid 5-oxo- tetrahydrofuran-2-ylmethyl ester (162.2 mg, 0.6 mmol) and the mixture was stirred overnight at 100 degrees C. The mixture was diluted with ethyl acetate, washed with sat. NH4CI, water and brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was dissolved in methanol- H2O (10:1 , 5.5 ml). To the solution was added KOH as 1 tablet. After stirring for 30min at room temperature, the mixture was concentrated under reduced pressure and the obtained residue was purified by silica-gel chromatography (hexane/EtOAc=4:1) to give the title compound (125 mg, 50%) as a solid. 1H NMR (CDCI3); 7.03-6.89 (m, 5H), 6.67 (d, 1 H), 4.06 (m, 1 H), 3.97 (ddd, 1 H), 3.85 (ddd, 1 H), 3.24 (dt, 1 H), 2.86 (m, 1 H), 2.64-2.50 (m, 3H), 2.25 (s, 3H), 2.17 (s, 3H), 2.04 (q, 4H), 1.93 (m, 2H), 1.79 (m, 1H), 1.50 (m, 1H), 0.88 (s, 9H), 0.59 (t, 6H); MS (ESI-) : 497 ([M-H]").

Example 51 Preparation of (S)-4-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-3-hydroxy- butyric acid

HOOCV0 OH

(1) Preparation of 3(S)-(tert-Butyl-dimethyl-silanyloxy)-4-hydroxy-butyric acid ethyl ester

EtOOC^V^OH ► EtOOC^V^OH OH OTBS To a stirred solution of 3(S),4-Dihydroxy-butyric acid ethyl ester (Tetrahedron A 992, 48(20), 4067.) (569 mg, 3.8 mmol) in DMF (12 ml) were added TBSCI (1.7 g, 11.2 mmol) and imidazole (1.55 g, 22.8 mmol) at room temperature and the mixture was stirred at room temperature for 12 h. The reaction mixture was poured into water and the products were extracted with ethyl acetate. The extracts were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was purified by silica gel chromatography (ethyl acetate/hexane = 1/40) to give disilylated compound (1.4g, 96%). To a stirred solution of the disilylated compound (1.33 g, 3.5 mmol) in MeOH (35 ml) was added PPTs (133 mg, 0.5 mmol) at room temperature and the mixture was stirred at room temperature for 17 h. The reaction mixture was poured into water and extracted with ethyl acetate. The extracts were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was purified by silica gel chromatography (ethyl acetate/hexane=1/5) to give the titled compound (393 mg, 43%). 1H-NMR (CDCI3): 0.09 (3H, s), 0.11 (3H, s), 0.90 (9H, s), 1.25(3H1 1), 1.92 (1 H, dd), 2.55 (2H, d), 3.45-3.70 (2H, m), 4.12 (2H, q), 4.15-4.30 (1H, s).

(2) Preparation of 3(S)-(tert-Butyl-dimethyl-silanyloxy)-4-(4-{1 -ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl -but-1-ynyl)- phenyl]-propyl}-2-methyl-phenoxy)-butyric acid ethyl ester

EtOOC'V^O OTBS

To a solution of 4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenol (compound prepared in Example 2-(2)) (255 mg, 0.502 mmol) and triphenylphosphine (145 mg, 0.552 mmol) in anhydrous Toluene (4 ml) was added dropwise DEAD (0.086 ml, 0.552 mmol) at 0 degrees C under nitrogen atmosphere, and the mixture was stirred at room temperature. To the reaction mixture, a solution of 3-(tert-Butyl-dimethyl-silanyloxy)-4- hydroxy-butyric acid ethyl ester (compound prepared in Example 51 -(1)) (158 mg, 0.602 mmol) in anhydrous Toluene (1 ml) was added. The resulting mixture was stirred at 60 degrees C for 5 h. After removal of solvent, diethyl ether was added and the resulting mixture was stirred for 1 h. The insoluble solid was filtered off. The filtrate was concentrated in vacuo and the obtained residue was purified by silica gel chromatography (ethyl acetate/hexane = 1/14) to give the titled compound (168 mg, 45%). 1H-NMR (CDCI3): 0.09 (s, 6H), 0.61 (t, 3H), 0.87 (s, 9H), 1.26 (t, 3H), 2.05 (q, 4H), 2.15 (s, 3H), 2.32 (s, 3H), 2.55 (dd, 1 H), 2.70 (dd, 1 H), 3.50 (s, 3H), 3.80 (dd, 1 H), 3.96 (dd, 1 H), 4.10-4.19 (m, 2H), 4.48-4.52 (m, 1 H), 5.15 (s, 2H), 6.67 (d, 1 H), 6.83 (s, 1 H), 6.89 (dd, 1 H), 7.00 (dd, 1 H), 7.06 (s, 1 H), 7.36 (d, 1 H); MS (ESI+) : 747([M+H]+).

(3) Preparation of (S)-4-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-3-hydroxy- butyric acid

^ooc^Cp^f Y T^ -- Hooc-r> OTBS I I X -V.C-F30M OH 3 A stirred solution of 3(S)-(tert-Butyl-dimethyl-silanyloxy)-4-(4-{1 -ethyl-1 -[3- methyl-4-(4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl -but-1-ynyl)- phenyl]-propyl}-2-methyl-phenoxy)-butyric acid ethyl ester (compound prepared in Example 51 -(2)) (143 mg, 0.19 mmol) in 1 ,4-dioxane (4 ml), cone. HCI (0.2 ml) was slowly added at 0 degrees C and the mixture was stirred at 50 degrees C for 10 h. The reaction mixture was neutralized by careful addition of sat. NaHCO3 solution and the products were extracted with ethyl acetate. The extracts were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was dissolved in MeOH (5 ml). To the mixture, 1N KOH aq. (0.55 ml, 0.55 mmol) was added at room temperature and the mixture was stirred for 5 h. The reaction mixture was concentrated in vacuo and poured into saturated NH4CI aq. The products were extracted with ethyl acetate. The extracts were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (ethyl acetate/hexane = 1/15) to give the titled compound (50 mg, 65%) as a white solid. 1H-NMR (CDCI3): 0.60 (t, 6H), 2.05 (q, 4H), 2.17 (s, 3H), 2.34 (s, 3H), 2.76 (t, 2H), 3.99 (d, 2H), 4.45 (m, 1 H), 6.68 (d, 1 H), 6.84 (s, 1 H), 6.92 (dd, 1 H), 6.97 (d, 1 H), 7.04 (s, 1 H), 7.34 (d, 1 H); MS(ESI-) : 559 ([M-H∏.

Example 52 Preparation of (S)-4-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xy)-3-hydroxy- butyric acid

HOOC^Y^0 OH (1) Preparation of (S)-3-(tert-Butyl-dimethyl-silanyloxy)-4-(4-{1 -ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-methoxymethoxy-3-trifluorome thyl-but-1 -enyl)- phenyl]-propyl}-2-methyl-phenoxy)-butyric acid ethyl ester

EtOOC^Y^O OTBS Using the same procedure as described for the preparation of Example 51- (2), the title compound was prepared from 4-{1-ethyl-1-[3-methyl-4-((E)- 4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-eny l)-phenyl]- propyl}-2-methyl-phenol (compound prepared in Example 30-(1 )). 1H-NMR (CDCI3): 0.09 (s, 6H), 0.61 (t, 3H), 0.87 (s, 9H), 1.26 (t, 3H), 2.05 (q, 4H), 2.15 (s, 3H), 2.32 (s, 3H), 2.55 (dd, 1 H), 2.70 (dd, 1 H), 3.50 (s, 3H), 3.80 (dd, 1 H), 3.96 (dd, 1 H), 4.10-4.19 (m, 2H), 4.48-4.52 (m, 1 H), 4.96 (s, 2H), 6.05 (d, 1 H), 6.68 (d, 1 H), 6.87-7.03 (m, 4H), 7.32 (d, 1 H), 7.36 (s, 1 H). (2) Preparation of (S)-4-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)-3- hydroxy-butyric acid

HOOi OH Using the same procedure as described for the preparation of Example 51- (3), the title compound was prepared from (S)-3-(tert-Butyl-dimethyl- silanyloxy)-4-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro -3-methoxymethoxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xy)-butyric acid ethyl ester (compound prepared in Example 52-(1 )). 1H-NMR (CDCI3): 0.61 (t, 6H), 2.05 (q, 4H), 2.17 (s, 3H), 2.34 (s, 3H), 2.76 (t, 2H), 3.99 (d, 2H), 4.45 (m, 1 H), 6.09 (d, 1 H), 6.69 (d, 1 H), 6.90-7.00 (m, 4H), 7.34 (t, 1 H), 7.35 (d, 1 H); MS (ESI-) : 561 ([M-H]").

Example 53 Preparation of (R)-4-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-3-hydroxy- butyric acid

HOOC'^Ό OH

(1 ) Preparation of 3(R)-(tert-butyl-dimethyl-silanyloxy)-4-hydroxy-butyric acid ethyl ester

EtOOC^V^OH ► EtOOC'V^0" OH OTBS Using the same procedure as described for the preparation of Example 51- (1 ), the title compound was prepared from 3(S),4-dihydroxy-butyric acid ethyl ester (compound prepared using the same procedure in Tetrahedron, 1992, 48(20), 4067.) from diethyl (R)-malate). 1H-NMR (CDCI3): 0.09 (3H, s), 0.11 (3H, s), 0.89 (9H, s), 1.25(3H, t), 1.92 (1 H, brt), 2.55 (2H, d), 3.45-3.70 (2H, m), 4.12 (2H, q), 4.15-4.30 (1H1 s).

(2) Preparation of (R)-3-(tert-Butyl-dimethyl-silanyloxy)-4-(4-{1-ethyl-1-[3- methyl-4-(4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl -but-1-ynyl)- phenyl]-propyl}-2-methyl-phenoxy)-butyric acid ethyl ester

EtOOC^V^O OTBS

Using the same procedure as described for the preparation of Example 51- (2), the title compound was prepared from 4-{1-ethyl-1-[3-methyl-4-(4,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-ynyl) -phenyl]-propyl}-2- methyl-phenol (compound prepared in Example 2-(2)) and 3(R)-(tert-Butyl- dimethyl-silanyloxy)-4-hydroxy-butyric acid ethyl ester (compound prepared in Example 53-(1)). 1H-NMR (CDCI3): 0.09 (s, 6H), 0.61 (t, 3H), 0.87 (s, 9H), 1.26 (t, 3H), 2.05 (q, 4H), 2.15 (s, 3H), 2.32 (s, 3H), 2.55 (dd, 1 H), 2.70 (dd, 1 H), 3.50 (s, 3H), 3.80 (dd, 1 H)1 3.96 (dd, 1 H), 4.10-4.19 (m, 2H), 4.48-4.52 (m, 1 H)1 5.15 (s, 2H), 6.67 (d, 1 H), 6.83 (s, 1 H), 6.89 (dd, 1 H), 7.00 (dd, 1 H), 7.06 (s, 1 H), 7.36 (d, 1 H).

(2) Preparation of (R)-4-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3 - trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-3-hydroxy- butyric acid

EtOOC^V^O' HOOC^^O OTBS OH

Using the same procedure as described for the preparation of Example 51- (3), the title compound was prepared from (R)-3-(tert-Butyl-dimethyl- silanyloxy)-4-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-m ethoxymethoxy-3- trifluoromethyl-but-i-ynyO-phenyll-propylJ^-methyl-phenoxyJ- butyric acid ethyl ester (compound prepared in Example 53-(2)). 1H-NMR (CDCI3): 0.59 (t, 6H), 2.03 (q, 4H), 2.15 (s, 3H), 2.38 (s, 3H), 2.76 (t, 2H), 3.99 (d, 2H), 4.45 (m, 1 H), 6.68 (d, 1 H), 6.84 (d, 1H), 6.92 (dd, 1 H), 6.97 (d, 1 H), 7.04 (s, 1 H), 7.34 (d, 1 H); MS (ESI-) : 559 ([M-H∏.

Example 54 Preparation of (R)-4-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xy)-3-hydroxy- butyric acid

H00C"~V^0 OH (1 ) Preparation of (R)-3-(tert-Butyl-dimethyl-silanyloxy)-4-(4-{1 -ethyl-1 -[3- methyl-4-((E)-4,4,4-trifluoro-3-methoxymethoxy-3-trifluorome thyl-but-1-enyl)- phenyl]-propyl}-2-methyl-phenoxy)-butyric acid ethyl ester

Etooc'^^cr ' ' CFT" — OTBS Using the same procedure as described for the preparation of Example 51- (2), the title compound was prepared from 4-{1 -ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-eny l)-phenyl]- propyl}-2-methyl-phenol (compound prepared in Example 30-(1)) and 3R- (tert-Butyl-dimethyl-silanyloxy)-4-hydroxy-butyric acid ethyl ester (compound prepared in Example 53-(1)). 1H-NMR (CDCI3): 0.09 (s, 6H), 0.61 (t, 3H), 0.87 (s, 9H), 1.26 (t, 3H), 2.05 (q, 4H), 2.15 (s, 3H), 2.32 (s, 3H), 2.55 (dd, 1H), 2.70 (dd, 1H), 3.50 (s, 3H), 3.80 (dd, 1 H), 3.96 (dd, 1H), 4.10-4.19 (m, 2H), 4.48-4.52 (m, 1H), 4.96 (s, 2H), 6.05 (d, 1 H), 6.68 (d, 1 H), 6.87-7.03 (m, 4H), 7.32 (d, 1 H), 7.36 (s, 1 H). (2) Preparation of (R)-4-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4 ,4 ,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)-3- hydroxy-butyric acid

EtOOC^g^O' HOOC^'^Ό OTBS OH Using the same procedure as described for the preparation of Example 51- (3), the title compound was prepared from (R)-3-(tert-Butyl-dimethyl- silanyloxy)-4-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro -3-methoxymethoxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xy)-butyric acid ethyl ester (compound prepared in Example 54-(1 )). 1H-NMR (CDCI3): 0.60 (t, 6H), 2.04 (q, 4H), 2.17 (s, 3H), 2.34 (s, 3H), 2.76 (t, 2H), 3.99 (d, 2H), 4.46 (m, 1 H), 6.08 (d, 1 H), 6.69 (d, 1 H), 6.90-7.00 (m, 4H), 7.26-7.39 (m, 2H); MS(ESI-) : 561 ([M-H]").

Example 55 Preparation of (S)-6-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xymethyl)- tetrahydro-pyran-2-one

OH

Preparation of (S)-6-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xymethyl)- tetrahydro-pyran-2-one

OH

To a solution of 4-{1 -ethyl-1 -[3-methyl-4-((E)-4 ,4 ,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenol (compound prepared in Example 30-(1 )) (50 mg, 0.384 mmol) in toluene (3 ml) were added triphenylphosphine (151 mg, 0.576 mmol), DEAD (0.09 ml, 0.576 mmol) and (S)-6-Hydroxymethyl-tetrahydro-pyran-2-one (J. Chem. Soc, Perkin Trans. 1, 2000, 20, 3519) (194 mg, 0.384 mmol) and the mixture was stirred at room temperature overnight and at 40 degrees C for 2 h. The mixture was filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (EtOAc:Hex=1 :5) to give (S)-6-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-tetrahydro-pyran-2-one (78mg, 33%). To a solution of (S)-6- (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-methoxymeth oxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)- tetrahydro-pyran-2-one (65 mg, 0.105 mmol) in CH2Cb (3 ml) at -30 degrees C was added TMSBr (0.017 ml, 0.126 mmol) and the mixture was stirred at - 30 degrees C for 1 h and at 0 degrees C for 30 min. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extracted with CH2CI2. The extracts were dried over sodium sulfate, filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (EtOAc:Hex=1 :4) to give the title compound (65 mg, 79%). 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.80-2.12 (m, 8H), 2.15 (s, 3H), 2.33 (s, 3H), 2.45-2.70 (m, 2H), 2.90 (t, 2H), 3.35 (s, 1 H), 4.01-4.14 (m ,2H), 4.66 (m, 1H), 6.07 (d, 1H), 6.67 (d, 1H), 6.87-7.01 (m, 4H), 7.32-7.39 (m, 2H); MS (ESI-) : 571 ([M-H]').

Example 56 Preparation of (S)-6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xy)-5-hydroxy- hexanoic acid

0 OH OH Preparation of (S)-6-(4-{1 -ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xy)-5-hydroxy- hexanoic acid

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-6-(4-{1-ethyl-1-[3-methyl-4- ((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl) -phenyl]-propyl}-2- methyl-phenoxymethyl)-tetrahydro-pyran-2-one (compound prepared in Example 55). The yield was 91%. 1H-NMR (300MHz1 CD3OD as potassium salt): 0.63 (t, 6H), 1.61-1.84 (m, 4H), 2.10 (q, 4H), 2.18 (s, 3H), 2.24 (t, 2H), 2.35 (s, 3H), 2.45-2.70 (m, 2H), 2.90 (t, 2H), 3.35 (s, 1H), 3.90-4.03 (m, 3H), 6.21(d, 1H), 6.79 (d, 1H), 6.89- 7.03 (m, 4H), 7.37 (d, 1H), 7.44 (d, 1H); MS (ESI-) : 589 ([M-H]").

Example 57 Preparation of (S)-6-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)- tetrahydro-pyran-2-one

OH

(1) Preparation of (S)-6-(4-{1-ethyl-1-[3-methyl-4-(4 ,4 ,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-tetrahydro-pyran-2-one OMOM

Using the same procedure as described for the preparation of Example 55, the title compound was prepared from 4-{1-ethyl-1-[3-methyl-4-(4,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenol (compound prepared in Example 2-(2)) and (S)-Q- hydroxymethyl-tetrahydro-pyran-2-one (J. Chem. Soc, Perkin Trans. 1, 2000, 20, 3519). The yield was 46%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.80-2.09 (m, 8H), 2.15 (s, 3H), 2.39 (s, 3H), 2.45-2.69 (m, 2H), 3.47 (s, 3H), 4.01-4.14 (m ,2H), 4.69 (m, 1 H), 5.15 (s, 2h), 6.67 (d, 1H), 6.84-7.04 (m, 4H), 7.36 (d, 1H).

(2) Preparation of (S)-6-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-pheno xymethyl)- tetrahydro-pyran-2-one

OH

To a solution of (S)-6-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-tetrahydro-pyran-2-one (compound prepared in Example 57-(1)) (78 mg, 0.127 mmol) in CH2CI2 (2 ml) at 0 degrees C were added thiophenol (0.020 ml, 0.190 mmol) and BF3-OEt2 (0.048 ml, 0.381 mmol) and the mixture was stirred at room temperature for 1 h. The reaction mixture was poured into phosphate buffer and the products were extracted with EtOAc. The extracts were dried over sodium sulfate, filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (EtOAc:Hex=1 :5) to give the title compound (45 mg, 62%). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.80-2.09 (m, 8H), 2.14 (s, 3H), 2.38 (s, 3H), 2.45-2.71 (m, 2H), 3.34 (s, 1 H), 4.01-4.14 (m ,2H), 4.67 (m, 1 H), 6.66 (d, 1H), 6.84-7.04 (m, 4H), 7.34 (d, 1H); MS (ESI+) : 571 ([M+H]+).

Example 58 Preparation of (S)-6-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-5-hydroxy- hexanoic acid

Preparation of (S)-6-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trif luoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-5-hydroxy- hexanoic acid

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (S)-6-(4-{1-Ethyl-1-[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenoxymethyl)-tetrahydro-pyran-2-one (compound prepared in Example 57-(2)). The yield was 99%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.62 (t, 6H), 1.58-1.88 (m, 4H), 2.10 (q, 4H), 2.18 (s, 3H), 2.24 (t, 2H), 2.38 (s, 3H), 3.89-4.02 (m ,3H), 6.80 (d, 1 H), 6.87-7.08 (m, 4H), 7.34 (d, 1H); MS (ESI-) : 587 ([M-H∏.

Example 59 Preparation of (R)-6-(4-{1 -Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)- tetrahydro-pyran-2-one

(1) Preparation of (R)-6-(4-{1 -Ethyl-1 -[3-methyl-4-(4 ,4 ,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-tetrahydro-pyran-2-one

Using the same procedure as described for the preparation of Example 55, the title compound was prepared from 4-{1-ethyl-1-[3-methyl-4-(4,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenol (compound prepared in Example 2-(2)) and (R)-6- hydroxymethyl-tetrahydro-pyran-2-one (J. Chem. Soc, Perkin Trans. 1, 2000, 20, 3519). The yield was 46%. 1H-NMR(CDCI3): 7.37(d, 1H), 7.04-6.84 (m, 4H), 6.67 (d, 1H), 5.15 (s, 2H), 4.69 (m, 1 H), 4.12 (m, 2H), 3.84 (s, 3H), 2.60 (m, 2H), 2.39 (s, 3H), 2.15 (s, 3H), 2.04 (m, 6H), 1.88 (m, 2H), 0.59 (t, 6H).

(2) Preparation of (R)-6-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-pheno xymethyl)- tetrahydro-pyran-2-one To a solution of (R)-6-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-tetrahydro-pyran-2-one (compound prepared in Example 59-(1)) (43 mg, 0.07 mmol) in CH2CI2 (3 ml) at -30 degrees C was added TMSBr (0.014 ml, 0.105 mmol) and the mixture was stirred at -30 degrees C for 1 h and at 0 degrees C for 30 min. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extracted with CH2CI2. The extracts were dried over sodium sulfate, filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (CH2CI2: MeOH=30:1) to give the title compound (21 mg, 53%). IH-NMR(CDCI3): 7.36 (d, 1H), 7.04 (s, 1H), 6.99 (s, 1 H), 6.91 (dd, 1H), 6.84 (d, 1 H), 6.66 (d, 1 H), 4.69 (m, 1 H), 4.09 (m, 2H), 2.58 (m, 2H), 2.38 (s, 3H), 2.15 (s, 3H), 2.04 (m, 6H), 1.88 (m, 2H), 0.59 (t, 6H); MS(ESI-) : 569 ([M-H]"

Example 60 Preparation of (R)-6-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-5-hydroxy- hexanoic acid

Preparation of (R)-6-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-5-hydroxy- hexanoic acid

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (R)-6-(4-{1-ethyl-1-[3-methyl-4- (4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenoxymethyl)-tetrahydro-pyran-2-one (compound prepared in Example 59-(2)). The yield was 99%. 1H-NMR (300MHz, CD3OD as potassium salt): 0.62 (t, 6H), 1.58-1.84 (m, 4H), 2.10 (q, 4H), 2.18 (s, 3H), 2.24 (t, 2H), 2.38 (s, 3H), 3.89-3.99 (m ,3H), 6.80 (d, 1H), 6.95-7.07 (m, 4H), 7.34 (d, 1H); MS (ESI-) : 587 ([M-K∏.

Example 61 Preparation of (R)-6-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xymethyl)- tetrahydro-pyran-2-one

(1) Preparation of (R)-6-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-tetrahydro-pyran-2-one

Using the same procedure as described for the preparation of Example 55, the title compound was prepared from 4-{1 -ethyl-1 -[3-methyl-4-((E)-4 ,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phe nyl]-propyl}-2- methyl-phenol (compound prepared in Example 30-(1)) and (R)-6- hydroxymethyl-tetrahydro-pyran-2-one (J. Chem. Soc, Perkin Trans. 1, 2000, 20, 3519). The yield was 35%. 1H-NMR (CDCI3): 7.36 (d, 1H), 7.02-6.89 (m, 4H), 6.67 (d, 1H), 6.05 (d,1H), 4.96 (s, 2H), 4.68 (m, 1 H), 4.09 (m, 2H), 3.50 (s, 3H), 2.57 (m, 2H), 2.32 (s,3H), 2.16 (s, 3H), 2.05 (m, 6H), 1.89 (m, 2H), 0.61 (t, 6H). (2) Preparation of (R)-6-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl- phenoxymethyl)-tetrahydro-pyran-2-one

o o Using the same procedure as described for the preparation of Example 59- (2), the title compound was prepared from (R)-6-(4-{1-ethyl-1-[3-methyl-4- ((E)-4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but- 1-enyl)-phenyl]- propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-one (compound prepared in Example 61 -(1)). The yield was 92%. 1H-NMR(CDCI3): 7.33 (d, 1H), 7.01-6.88 (m, 4H), 6.66 (d, 1H), 6.07 (d,1H), 4.67 (m, 1 H), 4.08 (m, 2H), 2.58 (m, 2H), 2.33 (3,3H), 2.15 (s, 3H), 2.04 (t, 6H), 1.88 (m, 2H), 0.61 (t, 6H); MS(ESI-) : 571.49 ([M-H∏.

Example 62 Preparation of (R)-6-(4-{1 -Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xy)-5-hydroxy- hexanoic acid

O OH Preparation of (R)-6-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xy)-5-hydroxy- hexanoic acid

OH

Using the same procedure as described for the preparation of Example 1- (7), the title compound was prepared from (R)-6-(4-{1 -ethyl-1 -[3-methyl-4- ((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl) -phenyl]-propyl}-2- methyl-phenoxymethyl)-tetrahydro-pyran-2-one (compound prepared in Example 61 -(2)). The yield was quant. 1H-NMR (300MHz, CD3OD as potassium salt): 8.44 (d, 1H), 8.35 (d, 1H), 7.99 (d, 1 H), 7.88 (d, 1 H), 7.78 (d, 1H),7.21 (d, 1 H), 4.92 (m, 3H), 3.35 (s, 3H), 3.24 (t, 2H), 3.17 (s, 3H), 3.10 (q, 4H), 2.91 (s, 3H), 2.73 (m, 2H), 2.61 (m, 1H), 1.6 (t, 6H); MS (ESI-) : 589 ([M-H]").

Example 63 Preparation of (S)-3-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol

HoΥ^o OH

(1) Preparation of 1-(4-{1-[4-((R)-2,2-dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-pent -1-yn-3-ol

To a solution of 4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(4)) (250 mg, 0.660 mmol) in anhydrous DMF (6.6 ml) were added NaOH (40 mg, 0.99 mmol) and toluene-4-sulfonic acid (S)-2,2-dimethyl-[1 ,3]dioxolan-4- ylmethyl ester (214 mg, 0.792 mmol) and the mixture was stirred at 60 degrees C for 11 h. The mixture was poured into saturated NH4CI aq. and the products were extracted with EtOAc. The extacts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by Silica gel chromatography (EtOAc:n- Hexane=1 :10) to give the title compound (177 mg, 56%) as a white solid. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.11 (t, 6H), 1.40 (s, 3H), 1.46 (s, 3H), 1.70-1.83 (m, 4H), 2.04 (q, 4H), 2.14 (s, 3H), 2.37 (s, 3H), 3.89-3.99 (m, 2H), 4.04-4.19 (m, 3H), 4.42-4.50 (m, 1H), 6.68 (d, 1 H), 6.84 (s, 1 H), 6.90 (d, 2H), 6.99 (S1 1H), 7.27 (d, 1H).

(2) Preparation of (S)-3-(4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol

To a solution of 1-(4-{1-[4-((R)-2,2-dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-3-ethyl-pent-1-yn-3-ol (compound prepared in Example 63-(1)) (104 mg, 0.211 mmol) in THF:H2O (4:1, 2.5 ml) was added TFA (1 ml, 12.98 mmol) and the mixture was stirred at 0 degrees C for 3 h. The mixture was poured into saturated NaHCO3 aq. and the products were extracted with EtOAc. The extacts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (EtOAc:n- Hexane=1 :1 ) to give the title compound (63mg, 66%). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.11 (t, 6H), 1.70-1.81 (m, 4H), 2.00 (m, 1H), 2.04 (q, 4H), 2.07 (s, 3H), 2.37 (s, 3H)1 2.52 (d, 1H), 3.82-3.90 (m, 2H), 4.03 (d, 2H), 4.11-4.17 (m, 1H), 6.69 (d, 1 H), 6.86 (d, 1 H), 6.90 (s, 1H), 6.94 (s ,1H), 6.99 (d, 1H), 7.27 (d, 1H); MS (ESI+) : 470 ([M+H]+).

Example 64 Preparation of (S)-3-(4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol

OH (1) Preparation of (E)-1-(4-{1-[4-((R)-2,2-dimethyl-[1 ,3]dioxolan-4- ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl) -3-ethyl-pent-1- en-3-ol

HO

To a solution of 4-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1- (5)) (150 mg, 0.394 mmol) in anhydrous DMF (6.6 ml) were added K2CO3 (136 mg, 0.985 mmol) and toluene-4-sulfonic acid (S)-2,2-dimethyl- [1 ,3]dioxolan-4-ylmethyl ester (169 mg, 0.591 mmol) and the mixture was stirred at 100 degrees C for 14 h. The mixture was poured into saturated NH4CI aq. and the products were extracted with EtOAc. The extacts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (EtOAc:n-Hexane=1 :7) to give the title compound (170 mg, 88%). 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 0.92 (t, 6H), 1.40 (s, 3H),1.46 (s, 3H), 1.63 (q, 4H), 2.04 (q, 4H), 2.16 (s, 3H), 2.31 (s, 3H), 3.89-4.16 (m, 4H), 4.48 (m, 1 H), 6.00 (d, 1 H), 6.68 (d, 1 H), 6.74 (s, 1 H), 6.91-6.97 (m, 4H), 7.29 (d, 1 H).

(2) Preparation of (S)-3-(4-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)- 3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol

Using the same procedure as described for the preparation of Example 63- (2), the title compound was prepared from (E)-1-(4-{1-[4-((R)-2,2-dimethyl- [1 ,3]dioxolan-4-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2- methyl- phenyl)-3-ethyl-pent-1-en-3-ol (compound prepared in Example 64-(1)). The yield was 38%. 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 0.92 (t, 6H), 1.65 (q, 4H), 2.00 (m, 1 H), 2.04 (q, 1 H), 2.17 (s,3H), 2.31 (s,3H), 2.52 (d, 1 H), 3.76-3.86 (m 2H), 4.03-4.04 (m, 2H), 4.08-4.14 (m, 1 H), 6.01 (d, 1 H), 6.72 (s, 1 H), 6.73 (d, 1 H), 6.91-6.98 (m, 4H), 7.29 (d, 1H).

Example 65 Preparation of (S)-3-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol

(1) Preparation of 3-(4-{1-[4-((S)-2,3-dihydroxy-propoxy)-3-methyl-phenyl]-1- ethyl-propyl}-2-methyl-phenyl)-propionic acid methyl ester

CO2CH3 HO" Y "O' ^T Y ^ "CO2CH3

To a solution of 3-{4-[1-ethyl-1-(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenylj-propionic acid methyl ester (compound prepared in Example 18-(2)) (320 mg, 0.90 mmol) in anhydrous DMF (9 ml) at room temperature under nitrogen atmosphere were added K2CO3 (248 mg, 1.80 mmol) and (S)-toluene-4-sulfonic acid 2,2-dimethyl-[1 ,3]dioxolan-4-ylmethyl ester (309 mg, 1.08 mmol). After stirring overnight at 100 degrees C, the reaction mixture was diluted with ethyl acetate, washed with sat. NH4CI, water and brine, and dried over MgSO4. The solution was concentrated under reduced pressure and the obtained residue was dissolved in methanol (9 ml). To the solution was added concentrated HCI with 4drops and the mixture was stirred at room temperature for 30 min. The mixture was concentrated under reduced pressure and the obtained residue was purified by silica-gel chromatography (hexane/EtOAc=7:1) to give the title compound (187 mg, 0.43 mmol, 48%). 1H NMR (CDCI3): 6.99-6.83 (m, 5H), 6.69 (d, 1 H), 4.10 (m, 1 H), 4.03 (dd, 2H), 3.82 (m, 2H), 3.67 (s, 3H), 2.89 (dt, 2H), 2.57 (dt, 2H), 2.25 (s, 3H), 2.16 (s, 3H), 2.04 (q, 4H), 0.59 (t, 6H).

(2) Preparation of (S)-3-(4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol

CO2CH3

To a solution of 3-(4-{1-[4-((S)-2,3-dihydroxy-propoxy)-3-methyl-phenyl]-1- ethyl-propyl}-2-methyl-phenyl)-propionic acid methyl ester (compound prepared in Example 65-(1)) (187 mg, 0.43 mmol) in anhydrous THF (4 ml_) under nitrogen atmosphere at 0 degrees C was added ethyl magnesium bromide (1.3 ml, 1.3 mmol, 1.0M in THF) and the mixture was stirred at 0 degrees C for 2 h. The mixture was poured into saturated NH4CI aq. and the products were extracted with EtOAc. The extacts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (EtOAc:n- Hexane=1 :7) to give the title compound (110 mg, 56%). 1H NMR (CDCI3); 7.01-6.89 (m, 5H), 6.69 (d, 1 H), 4.10 (m, 1 H), 4.02 (dd, 2H), 3.84 (dd, 1 H), 3.76 (dd, 1 H), 2.56 (m, 2H), 2.25 (s, 3H), 2.16 (s, 3H), 2.04 (q, 4H), 1.65 (m, 2H), 1.55 (q, 4H), 0.90 (t, 6H), 0.59 (t, 6H); MS (ESI-) : 455 ([M-H∏.

Example 66 Preparation of 3-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2(S)-diol (1) Preparation of 1-(4-{1-[4-((R)-2,2-dimethyl-[1,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl -pent-1-yn-3-ol

Using the same procedure as described for the preparation of Example 64- (1), the title compound was prepared from 4-{1-Ethyl-1-[4-(3-hydroxy-4,4- dimethyl-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phen ol (compound prepared in Example 3). The yield was 74%. 1H-NMR (300MHz, CDCI3): 0.58 (t, 6H), 1.06 (s, 9H), 1.40 (s, 3H), 1.45 (s, 3H), 1.76 (d, 1H), 2.03 (q, 4H), 2.14 (s, 3H), 2.37 (s, 3H), 3.89-3.98 (m, 2H), 4.03-4.16 (m, 2H), 4.25 (d, 1 H), 4.42-4.50 (m, 1 H), 6.68 (d, 1 H), 6.85-6.99 (m, 4H), 7.28 (d, 1H).

(2) Preparation of 3-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1,2(S)-diol

OH OH To a solution of 1-(4-{1-[4-((R)-2,2-dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl -pent-1-yn-3-ol (compound prepared in Example 66-(1 )) (134 mg, 0.272 mmol) in MeOH (6 ml) was added conc.HCI (0.23 ml, 2.72 mmol) and the mixture was stirred at room temperature for 1 h. The reaction mixture was neutralized by sat. NaHCO3 solution, extracted with CH2Cb, dried over MgSO-i, filtered, and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (EtOAc:hexane=1:1) to give the title compound (40 mg, 33 %). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.06 (s, 9H), 1.78 (d, 1 H), 1.98-2.07 (m, 5H), 2.15 (s, 3H), 2.37 (s, 3H), 2.54 (d, 1H), 3.73-3.89 (m, 2H), 4.03 (m, 2H), 4.11 (m, 1 H), 4.25 (d, 1 H), 6.69 (d, 1 H)1 6.86-6.99 (m, 4H), 7.28 (d, 1 H); MS (ESI+) : 475 (M+Na)+.

Example 67 Preparation of 3-(4-{1 -ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2(S)-diol

HO ' ' OH (1) Preparation of (E)-1-(4-{1-[4-((R)-2,2-dimethyl-[1 ,3]dioxolan-4- ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl) -4,4-dimethyl- pent-1-en-3-ol

OH

Using the same procedure as described for the preparation of Example 64- (1), the title compound was prepared from 4-{1 -ethyl-1 -[4-((E)-3-hydroxy-4 ,4- dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phen ol (compound prepared in Example 14). The yield was 74%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 0.96 (s, 9H), 1.40 (s, 3H), 1.45 (s, 3H), 2.04 (q, 4H), 2.15 (s, 3H), 2.29 (s, 3H), 3.89-3.98 (m, 3H), 4.04-4.08 (m, 1 H), 4.13-4.18 (m, 1 H), 4.42-4.49 (m, 1 H), 6.12 (dd, 1 H), 6.67-6.76 (m, 2H), 6.68-6.96 (m, 4H), 7.31 (d, 1H).

(2) Preparation of 3-(4-{1 -ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1 - enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2(S)-diol HO O' OH HO

To a solution of (E)-1-(4-{1-[4-((R)-2,2-dimethyl-[1 ,3]dioxolan-4-ylmethoxy)- 3-methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-4,4-dinnet hyl-pent-1-en-3- ol (compound prepared in Example 67-(1)) (201 mg, 0.406 mmol) in THF/H2O (10/1 , 8 ml) was added 10-camphorsulfonic acid (289 mg, 1.21 mmol) and the mixture was stirred at 50 degrees C for 1 h. The reaction mixture was poured into sat. NaHCO3 solution, extracted with CH2CI2, dried over MgSO4, filtered, and concentrated under reduced pressure. The obtained residue was purified by ODS chromatography (MeOH/ H2O) to give the title compound (24.8 mg, 13%). 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 0.96 (s, 9H), 1.50 (m, 1H), 1.96-2.08 (m, 5H), 2.16 (s, 3H), 2.29 (s, 3H), 2.53 (d, 1H), 3.74-3.93 (m, 3H), 4.02-4.04 (m, 2H), 4.07-4.15 (m, 1H), 4.42-4.49 (m, 1 H), 6.12 (dd, 1 H), 6.68-6.76 (m, 2H), 6.90-6.98 (m, 4H), 7.30 (d, 1 H); MS (ESI+) : 477 ([M+Na]+).

Example 68 Preparation of 3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-propane- 1 ,2(S)-diol

HO

(1 ) Preparation of (R)-4-{4-[1-Ethyl-1-(4-ethynyl-3-methyl-phenyl)-propyl]-2- methyl-phenoxymethyl}-2,2-dimethyl-[1 ,3]dioxolane Using the same procedure as described for the preparation of Example 64- (1 ), the title compound was prepared from 4-[1 -ethyl- 1 -(4-ethynyl-3-methyl- phenyl)-propyl]-2-methyl-phenol (compound prepared in Example 1-(3)). The yield was 43%. 1H-NMR (300MHz, CDCI3): 7.33 (1 H, d), 7.01 (1 H, d), 6.95 (1 H, d), 6.91 (1 H, m), 6.86 (1 H, d), 6.69 (1 H, d), 4.46 (1 H, m), 4.11 (2H, m), 3.94 (2H, m), 2.39 (3H, s), 2.15 (3H1 s), 2.04 (4H, q), 1.46 (3H, s), 1.40 (3H1 s), 0.59 (6H, t).

(2) Preparation of 4-(4-{1-[4-((R)-2,2-dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-1 ,1 ,1-trifluoro-2- trifluoromethyl-but-3-yn-2-ol

To a solution of (R)-4-{4-[1-ethyl-1-(4-ethynyl-3-methyl-phenyl)-propyl]-2- methyl-phenoxymethyl}-2,2-dimethyl-[1 ,3]dioxolane (compound prepared in Example 68-(1 )) (540 mg, 1.328 mmol) in anhydrous THF (15 ml) at -78 degrees C under nitrogen atmosphere was added n-BuLi (2.5N, 0.585 ml, 1.462 mmol) dropwise and the mixture was stirred for 20 min. Then to the mixture, hexafluoroacetone was added until the solution was made colorless. The reaction mixture was poured into saturated NH4CI aq. and the products were extracted with diethyl ether. The extacts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (EtOAc:n- Hexane=1 :8) to give the title compound (686 mg, 90%). 1H-NMR (300MHz, CDCI3): 7.32 (1H, d), 7.04 (1H, d), 6.96 (1H, dd), 6.90 (1 H, dd), 6.82 (1 H, d), 6.67 (1 H, d), 4.46 (1 H, m), 4.42 (1 H, s), 4.10 (2H1 m), 3.94 (2H, m), 2.37 (3H, s), 2.13 (3H, s), 2.04 (4H, q), 1.46 (3H, s), 1.40 (3H, s), 0.59 (6H, t). (3) Preparation of (S)-3-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3 - trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-propane-1 ,2- diol

To a solution of 4-(4-{1-[4-((R)-2)2-dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-1 ,1 ,1 -trifluoro-2- trifluoromethyl-but-3-yn-2-ol (compound prepared in Example 68-(2)) (98 mg, 0.171 mmol) in THF (6 ml) was added 2N-HCI (2 ml) and the mixture was stirred at room temperature for 10 h. The reaction mixture was poured into water and the products were extracted with diethyl ether. The extracts were washed with brine and dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (n-Hexane:EtOAc=1 :1) to give the title compound (83.5 mg, 92%). 1H-NMR (300MHz, CDCI3): 7.34 (1H, d), 7.04 (1H, s), 6.96 (1H, dd), 6.92 (1 H, dd), 6.83 (1 H, d), 6.68 (1 H, d), 4.11 (1 H, m), 4.03 (1 H, s), 4.02 (2H, d), 3.82 (2H, m), 2.61 (1 H, d), 2.37 (3H, s), 2.14(3H, s), 2.04 (4H, q), 1.64 (1 H, s), 0.60 (6H, t); MS (ES-) : 531.08 ([M-H]").

Example 69 Preparation of (S)-3-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xy)-propane-1 ,2- diol (1 ) Preparation of (E)-4-(4-{1-[4-((R)-2(2-dimethyl-[1 ,3]dioxolan-4- ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl) -1,1,1-trifluoro- 2-trifluoromethyl-but-3-en-2-ol

To a solution of 4-(4-{1 -[4-((R)-2,2-dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-ph8nyl]-1-ethyl-propyl}-2-methyl-phenyl)-1 ,1 ,1-trifluoro-2- trifluoromethyl-but-3-yn-2-ol (compound prepared in Example 68-(2)) (168 mg, 0.293 mmol) in anhydrous THF (5 ml) was added LiAIH4 (0.350 ml, 0.350 mmol) at room temperature under N2 atmosphere and the mixture was stirred for 1 h and refluxed for 1 h. The reaction mixture was poured into saturated NH4CI aq. and the products were extracted with diethyl ether. The extacts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (EtOAc:n-Hexane=1 :8) to give the title compound (154 mg, 91 %). 1H-NMR (300MHz, CDCI3): 7.37 (1H, d), 7.33 (1 H, d), 7.01 (1 H, d), 6.94 (1 H, s), 6.91 (1 H, m), 6.88 (1H1 d), 6.68 (1 H, d), 6.10 (1H, d), 4.46 (1H, m), 4.11 (2H, m), 3.94 (2H, m), 3.33 (1H, s), 2.33 (3H, s), 2.16 (3H, s), 2.05 (4H, q), 1.45 (3H, s), 1.40 (3H, s), 0.60 (6H, t).

(2) Preparation of (S)-3-(4-{1~ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- propane-1 ,2-diol

Using the same procedure as described for the preparation of Example 68- (3), the title compound was prepared from (E)-4-(4-{1-[4-((R)-2,2-dimethyl- [1 ,3]dioxolan-4-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2- methyl- phenyl)-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2-ol (compound prepared in Example 69-(1 )). The yield was 74%. 1H-NMR (300MHz, CDCI3): 7.37 (1 H, d), 7.33 (1 H, d), 7.00 (1 H, d), 6.98 (1 H, s), 6.94 (1 H, dd), 6.89 (1 H, d), 6.70 (1 H, d), 6.08 (1 H, d), 4.11 (1 H, m), 4.04 (1 H, s), 4.02 (1 H1 d), 3.81 (2H, m), 3.36 (1 H, s), 2.57 (1 H, d), 2.33 (3H, s), 2.16 (3H, s), 2.05(4H, q), 2.04(1H, s), 0.60 (6H, t); MS (ES-) : 533 ([M-HV).

Example 70 Preparation of (S)-3-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-phenoxy)-pro pane-1 ,2-diol

HO (1 ) Preparation of 4-(4-{1-[4-((R)-2,2-dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-1 ,1 ,1 -trifluoro-2- trifluoromethyl-butan-2-ol

To a solution of 4-(4-{1-[4-((R)-2,2-dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-1 ,1 ,1-trifluoro-2- trifluoromethyl-but-3-yn-2-ol (compound prepared in Example 68-(2)) (110 mg, 0.192 mmol) in MeOH (5 ml) was added Pd-C (20 mg, 10 wt%). The mixture was stirred at room temperature for 20 h under H2 atmosphere. The mixture was filtered through celite 545, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (EtOAc:n-Hex=1 :7) to give the title compound (106 mg, 96%). 1H-NMR (300MHz, CDCI3): 7.02-6.88 (5H, m), 6.68 (1H, d), 4.46 (1H, m), 4.16 (1 H, dd), 4.06 (1 H, dd), 3.94 (2H, m), 3.12 (1 H, s), 2.80 (2H, dd), 2.25 (3H, s), 2.16 (3H, s), 2.15 (2H1 m), 2.03 (4H, q), 1.46 (3H, s), 1.40 (3H, s), 0.59 (6H1 1).

(2) Preparation of (S)-3-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-phenoxy)-p ropane-1 ,2-diol

HO

Using the same procedure as described for the preparation of Example 68- (3), the title compound was prepared from 4-(4-{1-[4-((R)-2,2-dimethyl- [1 ,3]dioxolan-4-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2- methyl- phenyl)-1 ,1 ,1-trifluoro-2-trifluoromethyl-butan-2-ol (compound prepared in Example 70-(1)). The yield was 73%. 1H-NMR (300MHz, CDCI3): 7.02-6.88 (5H, m), 6.70 (1 H, d), 4.11 (1 H, m), 4.04 (1 H, s), 4.03 (1 H, s), 3.82 (2H, m), 3.43 (1 H, brd), 2.80 (2H, dd), 2.65 (1 H, brd), 2.25 (3H, s), 2.16 (3H, s), 2.15 (2H, m), 2.03 (4H, q), 0.59 (6H, t); MS (ES-) : 535 ([M-H]").

Example 71 Preparation of 2-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol

(1) Preparation of 1-(4-{1-[4-(2,2-dimethyl-[1 ,3]dioxan-5-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-pent -1-yn-3-ol

HO To a solution of 4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(4)) (205 mg, 0.542 mmol) in anhydrous DMF (5.4 ml) were added K2CO3 (187 mg, 1.36 mmol) and toluene-4-sulfonic acid 2,2-dimethyl-[1 ,3]dioxan-5-ylmethyl ester (prepared from following procedure as described in Tetrahedron, 1991, 47, 1001.) (244 mg, 1.355 mmol) and the mixture was stirred at 110 degrees C for 15 h. The reaction mixture was poured into saturated NH4CI aq. and the products were extracted with EtOAc. The extacts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (EtOAc:n- Hexane=1 :6) to give the title compound (184 mg, 67%) . 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.11 (t, 6H), 1.43 (s, 3H), 1.46 (s, 3H), 1.72-1.85 (m, 4H), 2.04 (q, 4H), 2.14 (s, 3H), 2.13-2.20 (m, 1 H), 2.37 (s, 3H), 3.89-4.20 (m, 5H), 6.68 (d, 1 H), 6.84 (s, 1H), 6.91-6.94 (m, 2H), 6.99 (s, 1 H)1 7.27 (d, 1 H).

(2) Preparation of 2-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol

Using the same procedure as described for the preparation of Example 63- (2), the title compound was prepared from 1-(4-{1-[4-(2,2-Dimethyl- [1 ,3]dioxan-5-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-me thyl-phenyl)- 3-ethyl-pent-1-yn-3-ol (compound prepared in Example 71 -(1)). The yield was 38%. 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 0.92 (t, 6H), 1.57-1.70 (m, 4H), 2.04 (q, 4H), 2.15 (s,3H), 2.26 (t, 3H), 2.31 (s,3H), 3.95 (d, 4H), 4.09 (d, 2H), 6.70 (d, 1 H), 6.82 (s, 1H), 6.88 (d, 2H), 6.98 (s, 1H), 7.27 (d, 1H); MS (ESI-) : 465 ([M-H]-). Example 72 Preparation of 2-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol

HO

(1) Preparation of (E)-1-(4-{1-[4-(2,2-dimethyl-[1 ,3]dioxan-5-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-pent -1-en-3-ol

Using the same procedure as described for the preparation of Example 71- (1), the title compound was prepared from 4-{1-ethyl-1-[4-((E)-3-ethyl-3- hydroxy-pent-1 -enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(5)). The yield was 85%. 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 0.92 (t, 6H), 1.43 s, 3H), 1.46 (s, 3H), 1.64 (q, 4H), 2.04 (q, 4H), 2.15 (s, 3H), 2.18 (m, 1 H), 2.31 (s, 3H), 3.89- 4.20 (m, 6H), 6.01 (d, 1 H), 6.68 (d, 1 H), 6.74 (d, 1 H), 6.90-7.02 (m, 4H), 7.29 (d, 1 H).

(2) Preparation of 2-(4-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol

Using the same procedure as described for the preparation of Example 63- (2), the title compound was prepared from (E)-1-(4-{1-[4-(2,2-dimethyl- [1 ,3]dioxan-5-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-me thyl-phenyl)- 3-ethyl-pent-1-en-3-ol (compound prepared in Example 72-(1)). The yield was 44%. 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 0.92 (t, 6H), 1.57-1.70 (m, 6H), 2.04 (q, 4H), 2.15 (s,3H), 2.26 (m, 3H), 2.31 (s,3H), 3.95 (d, 4H), 4.09 (d, 2H), 6.01 (d, 1 H), 6.71 (d, 1H), 6.74 (s, 1H), 6.89 (d, 1H), 6.96-7.02 (m, 3H), 7.32 (d, 1H); MS (ESI-) : 467 ([M-H]").

Example 73 Preparation of 2-(4-{1 -ethyl-1-[4-(3-ethyl-3-hydroxy-pentyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxymethyl)-propane-1,3-diol

HO (1) Preparation of 1-(4-{1-[4-(2,2-dimethyl-[1 ,3]dioxan-5-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-pent an-3-ol

Using the same procedure as described for the preparation of Example 71- (1), the title compound was prepared from 4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy- pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared by hydrogenation of 4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (Example 1-(4)). The yield was 73%. 1H-NMR(300MHz, CDCI3): 0.60 (t, 6H), 0.91 (t, 6H), 1.43 (s, 3H), 1.46 (s, 3H), 1.55 (m, 6H), 1.63-1.69 (m, 1H), 2.02 (q, 4H), 2.14 (s, 3H), 2.18 (m, 1H), 2.26 (s, 3H), 2.55 (m, 2H), 3.89-4.16 (m, 6H), 6.68 (d, 1 H), 6.90-6.97 (m, 4H), 7.00 (d, 1H); MS (ESI+) : 528 ([M+NH4]+)

(2) Preparation of 2-(4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol Using the same procedure as described for the preparation of Example 63- (2), the title compound was prepared from 1-(4-{1-[4-(2,2-Dimethyl- [1 ,3]dioxan-5-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-me thyl-phenyl)- 3-ethyl-pentan-3-ol (compound prepared in Example 73-(1)). The yield was 73%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (t, 6H), 1.54 (q, 4H), 1.65 (m, 2H), 2.00 (q, 4H), 2.15 (s,3H), 2.25 (m, 1H), 2.31 (s,3H), 2.53-2.59 (m, 2H), 3.93 (d, 4H), 4.07 (d, 2H), 6.70 (d, 1 H), 6.91-7.00 (m, 5H); MS (ESI-) : 469 ([M-H]").

Example 74 Preparation of 2-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol

HO' HO (1 ) Preparation of 1-(4-{1-[4-(2,2-dimethyl-[1 ,3]dioxan-5-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl -pent-1-yn-3-ol

HO' OH OH Using the same procedure as described for the preparation of Example 71- (1 ), the title compound was prepared from 4-{1 -ethyl-1 -[4-(3-hydroxy-4, 4- dimethyl-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phen ol (compound prepared in Example 3). The yield was 68%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.06 (s, 9H), 1.43 (s, 3H), 1.46 (s, 3H), 1.76 (d, 1 H), 2.10 (q, 4H), 2.13 (s, 3H), 2.16-2.23 (m, 1H), 2.38 (s, 3H), 3.92 (dd, 2H), 4.00 (d, 2H), 4.06 (dd, 2H), 4.25 (d, 2H), 6.68 (d, 1 H), 6.84- 7.00 (m, 4H), 7.27 (d, 1H); MS (ESI+) : 524 ([M+NH4]+).

(2) Preparation of 2-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1,3-d iol

OH "" OH Using the same procedure as described for the preparation of Example 68- (2), the title compound was prepared from 1-(4-{1-[4-(2,2-dimethyl- [1 ,3]dioxan-5-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-me thyl-phenyl)- 4,4-dimethyl-pent-1-yn-3-ol (compound prepared in Example 74-(1)). The yield was 57%. 1 H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.06 (s, 9H), 1.79 (d, 1 H), 2.10 (q, 4H), 2.14 (s, 3H), 2.25 (m, 1 H), 2.38 (s, 3H), 3.93-3.96 (m, 4H), 4.09 (d, 2H), 4.25 (d, 1 H), 6.71 (d, 1H), 6.85-6.99 (m, 4H), 6.97-7.05 (m, 4H), 7.27 (d, 1 H); MS (ESI-) : 465 ([M-H]").

Example 75 Preparation of 2-(4-{1 -ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1,3-d iol

HO' OH HO (1 ) Preparation of (E)-1-(4-{1-[4-(2,2-dimethyl-[1 ,3]dioxan-5-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl -pent-1-en-3-ol OH Using the same procedure as described for the preparation of Example 71- (1), the title compound was prepared from 4-{1-ethyl-1-[4-((E)-3-hydroxy-4,4- dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phen ol (compound prepared in Example 14). The yield was 53%. 1 H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 0.96 (s, 9H), 1.43 (s, 3H), 1.46 (s, 3H), 1.51 (d, 1H), 2.04 (q, 4H), 2.14 (s, 3H), 2.20 (m, 1H), 2.29 (s, 3H), 3.89- 4.09 (m, 7H), 6.12 (dd, 1 H), 6.68 (d, 1 H), 6.73 (d, 1 H), 6.90-6.96 (m, 4H), 7.31 (d, 1H); MS (ESI+) : 526 ([M+NH4∏.

(2) Preparation of 2-(4-{1-ethyl-1-[4-((E)-3-hydroxy-4,4-dimethyl-pent-1- enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-propa ne-1 ,3-diol

OH OH

Using the same procedure as described for the preparation of Example 63- (2), the title compound was prepared from (E)-1-(4-{1-[4-(2,2-dimethyl- [1 ,3]dioxan-5-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-me thyl-phenyl)- 4,4-dimethyl-pent-1-en-3-ol (compound prepared in Example 75-(1)). The yield was 30%. 1H-NMR (300MHz, CDCI3): 0.68 (t, 6H), 1.04 (s, 9H), 1.59 (m, 1 H), 2.13 (q, 4H), 2.22 (s, 3H), 2.29-2.37 (m, 1 H), 2.37 (s, 3H), 3.98-4.04 (m, 5H), 4.17 (d, 2H), 6.19 (dd, 1H), 6.78-6.84 (m, 2H), 6.97-7.05 (m, 4H), 7.38 (d, 1H); MS (ESI-) : 467 ([M-H]").

Example 76 Preparation of 2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol OH HO Preparation of 2-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-propane-1 ,3-diol

OH Using the same procedure as described for the preparation of Example 65, the title compound was prepared from 4-{1-Ethyl-1-[4-((E)-3-hydroxy-4 ,4- dimethyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phen ol (compound prepared in Example 18) and toluene-4-sulfonic acid 2,2-dimethyl- [1 ,3]dioxan-5-ylmethyl ester (prepared from following procedure as described in Tetrahedron, 1991, 47, 1001.). The yield was 36%. 1H NMR (CDCI3): 7.03-6.89 (m, 5H), 6.71 (d, 1H), 4.09 (d, 2H), 3.95 (d, 4H), 3.24 (dt, 1 H), 2.85 (m, 1 H), 2.55 (m, 1 H), 2.25 (s, 3H), 2.15 (s, 3H), 2.04 (q, 4H), 1.79 (m, 1 H), 1.50 (m, 1 H), 0.89 (s, 9H), 0.59 (t, 6H); MS (ESI-) : 469 ([M-H]").

Example 77 Preparation of 2-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)- propane-1 ,3-diol

(1) Preparation of 5-{4-[1-ethyl-1-(4-ethynyl-3-methyl-phenyl)-propyl]-2- methyl-phenoxymethyl}-2,2-dimethyl-[1 ,3]dioxane Using the same procedure as described for the preparation of Example 71- (1 ), the title compound was prepared from 4-[1-ethyl-1-(4-ethynyl-3-methyl- phenyl)-propyl]-2-methyl-phenol (compound prepared in Example 1-(3)). The yield was 73%. 1H NMR (CDCI3): 7.33 (d, 1 H), 7.00-6.84 (m, 4H), 6.68 (d, 1 H), 4.10-3.89 (m, 6H), 3.21 (s, 1H), 2.39 (s, 3H), 2.18-2.02 (m, 1 H), 2.00 (s, 3H), 2.03 (q, 4H), 1.15 (s, 6H), 0.59 (t, 3H).

(2) Preparation of 4-(4-{1-[4-(2,2-Dimethyl-[1 ,3]dioxan-5-ylmethoxy)-3- methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-1 ,1 ,1 -trifluoro-2- trifluoromethyl-but-3-yn-2-ol

Using the same procedure as described for the preparation of Example 68- (2), the title compound was prepared from 5-{4-[1-Ethyl-1-(4-ethynyl-3- methyl-phenyl)-propyl]-2-methyl-phenoxymethyl}-2,2-dimethyl- [1 ,3]dioxane (compound prepared in Example 77-(1 )). The yield was 69%. 1H NMR (CDCI3): 7.33 (d, 1 H), 7.00-6.84 (m, 4H), 6.68 (d, 1 H), 4.13-3.89 (m, 6H), 3.45 (s, 1 H), 2.38 (s, 3H), 2.20-2.16 (m, 1 H), 2.08 (s, 3H), 2.03 (q, 4H), 1.46 (s, 3H), 1.43 (s, 3H), 0.59 (t, 3H).

(3) Preparation of 2-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)- propane-1 ,3-diol XT Tl Ho -λJ τ I ^S^CF3 Λ OH CF3 J^r I ODH CF3 Using the same procedure as described for the preparation of Example 66- (2), the title compound was prepared from 4-(4-{1-[4-(2,2-dimethyl- [1 ,3]dioxan-5-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-me thyl-phenyl)- 1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-yn-2-ol (compound prepared in Example 77-(2)). The yield was 69%. 1H NMR (CDCI3): 7.34 (d, 1 H)1 7.00-6.82 (m, 4H), 6.70 (d, 1 H), 4.08 (d, 2H), 3.95 (m, 4H), 3.83 (s, 1 H), 2.38 (s, 3H), 2.27-2.24 (m, 1 H)1 2.13 (s, 3H), 2.03 (q, 4H), 0.59 (t, 3H); MS (ESI-) : 545 ([M-H]").

Example 78 Preparation of 2-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)- propane-1 ,3-diol

(1 ) Preparation of (E)-4-(4-{1-[4-(2,2-dimethyl-[1 ,3]dioxan-5-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-1 ,1 ,1-trifluoro-2- trifluoromethyl-but-3-en-2-ol

CF?H

Using the same procedure as described for the preparation of Example 69- (1 ), the title compound was prepared from 4-(4-{1-[4-(2,2-dimethyl- [1 ,3]dioxan-5-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-me thyl-phenyl)- 1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-yn-2-ol (compound prepared in Example 77-(2)). The yield was 39%. 1H NMR (CDCI3); 7.39-7.32 (m, 2H), 7.01-6.86 (m, 4H), 6.69 (d, 1 H), 6.10 (d, 1 H), 4.15-3.89 (m, 6H), 3.11 (s, 1 H), 2.33 (s, 3H), 2.20-2.16 (m, 1 H), 2.08 (s, 3H), 2.03 (q, 4H), 1.46 (s, 3H), 1.43 (s, 3H), 0.59 (t, 3H).

(2) Preparation of 2-(4-{1-ethyl-1-[3-methyl-4-((E)-4)4,4-trifluoro-3-hydroxy-3 - trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)- propane-1 ,3-diol

"O' ~" ° HO Using the same procedure as described for the preparation of Example 66- (2), the title compound was prepared from (E)-4-(4-{1-[4-(2,2-dimethyl- [1 ,3]dioxan-5-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-me thyl-phenyl)- 1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2-ol (compound prepared in Example 78-(1 )). The yield was 83%. 1H NMR (CDCI3): 7.39-7.32 (m, 2H), 7.02-6.88 (m, 4H), 6.67 (d, 1H), 6.10 (d, 1 H), 4.12 (d, 2H), 3.96 (d, 4H), 3.18 (s, 1 H), 2.33 (s, 3H), 2.27-2.16 (m, 1 H), 2.08 (s, 3H), 2.04 (q, 4H), 0.59 (t, 3H); MS (ESI-) : 547 ([M-H]").

Example 79 Preparation of 2-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-phenoxymethy l)-propane-1 ,3- diol

Preparation of 2-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-butyl)-phenyl]-propyl}-2-methyl-phenoxymethy l)-propane-1 ,3- diol CF?H

To a solution of 2-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4 ,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy methyl)- propane-1 ,3-diol (compound prepared in Example 78-(2)) (50 mg, 0.091 mmol) in MeOH (5 ml) was added Pd(OH)2/C (5 mg, 10 wt%). The mixture was stirred at room temperature for 3 h under H2 atmosphere. The mixture was filtered through celite 545, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel chromatography (n-Hexane: CH2CI2: EtOAc=I :1 :1) to give the title compound (28.5 mg, 57%). 1H NMR (CDCI3): 7.01-6.90 (m, 5H), 6.72 (d, 1 H), 6.67 (d, 1 H), 6.10 (d, 1 H)1 4.09 (d, 2H), 3.96 (d, 2H), 3.95 (d, 2H), 3.13 (s, 1 H), 2.79 (dd, 2H), 2.25 (s, 3H), 2.18-2.00 (m, 6H), 2.15 (s, 3H), 0.59 (t, 3H); MS (ESI-) : 549 ([M-H]").

Example 80 Preparation of 5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid

(1) Preparation of 5-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid ethyl ester

EtOOC

To a solution of 4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 18) (200 mg, 0.52 mmol) in DMF (5 ml) were added K2CO3 (144 mg, 1.04 mmol) and ethyl-5-bromovalerate (0.169 ml, 1.04 mmol) and the mixture was stirred at 70 degrees C for 13 h. The reaction mixture was cooled to room temperature, poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1:10) to give the title compound (170 mg, 64%). 1H-NMR (300MHz, CDCI3): 0.6 (t, 6H), 0.89 (s, 9H), 1.25 (t, 3H), 1.52 (m, 1 H), 1.81 (m, 5H), 2.05 (q, 4H), 2.16 (s,3H), 2.26 (s,3H), 2.39 (m, 2H), 2.56 (m, 1H), 2.85 (m, 1 H), 3.26 (m, 1H), 3.94 (t, 2H), 4.12 (q, 2H), 6.66 (d, 1H), 6.90 (m, 4H), 7.02 (d, 1 H).

(2) Preparation of 5-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid

I T OH ' • OH To a stirred solution of 5-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid ethyl ester (compound prepared in Example 80-(1)) (170 mg, 0.333 mmol) in MeOH (3 ml) was added 1 N-KOH (1.OmI, 1.0 mmol) and the mixture was stirred at room temperature for 5 h. The reaction mixture was poured into 1 N-HCI and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n- Hexane (1 :3) to give the title compound (108 mg, 67%). 1H-NMR (300MHz, CDCI3): 0.6 (t, 6H), 0.89 (s, 9H), 1.52 (m, 1 H), 1.81 (m, 1 H), 1.86 (m, 4H), 2.05 (q, 4H), 2.16 (s,3H), 2.26 (s,3H), 2.46 (m, 2H), 2.56 (m, 1 H), 2.85 (m, 1 H), 3.26 (m, 1 H), 3.94 (t, 2H), 6.66 (d, 1 H), 6.90 (m, 4H), 7.02 (d, 1 H); MS (ESI-) : 481 ([M-H]").

Example 81 Preparation of 5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid

o HO OH (1 ) Preparation of 5-(4-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid ethyl ester

o HO ^r ^T ^=X Eto' ^" ^^ ^o' OH s r OH " Using the same procedure as described for the preparation of Example 80- (1 ), the title compound was prepared from 4-{1-ethyl-1-[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno l (compound prepared in Example 1-(5)). The yield was 87%. 1H-NMR (300MHz1 CDCI3): 0.61 (t, 6H), 0.92 (t, 6H), 1.25 (t,3H), 1.64 (q, 4H), 1.84 (m, 4H), 2.04 (q, 4H), 2.16 (s, 3H), 2.31 (s, 3H), 2.39 (t, 2H), 3.95 (t, 2H), 4.14 (q, 2H), 5.99 (d, 1 H), 6.66 (d, 1 H), 6.74 (d, 1 H), 6.91-6.96 (m, 4H), 7.29 (d, 1 H) ; MS (ESI+) : 531 ([M+Na]+).

(2) Preparation of 5-(4-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid

o O EtO HO OH f OH Using the same procedure as described for the preparation of Example 80- (2), the title compound was prepared from 5-(4-{1-ethyl-1-[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-pentanoic acid ethyl ester (compound prepared in Example 81 -(1)). The yield was 82%. 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 0.92 (t, 6H), 1.64 (q, 4H), 1.85 (m, 1 H), 2.04 (q, 4H), 2.15 (s, 3H), 2.31 (s, 3H), 2.46 (t, 2H), 3.95 (t, 2H), 5.99 (d, 1 H)1 6.66 (d, 1 H), 6.74 (d, 1 H), 6.91-6.96 (m, 4H), 7.29 (d, 1 H) ; MS (ESI- ) : 479 ([M-H]-).

Example 82 Preparation of 5-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid

o HO

Preparation of 5-(4-{1 -ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid

Using the same procedure as described for the preparation of Example 80- (1 ), 5-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-pentanoic acid ethyl ester was prepared from 4- {1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl-phenyl]-propyl}-2- methyl-phenol (compound prepared in Example 1-(4)). The yield was 53%. Using the same procedure as described for the preparation of Example 80- (2), the title compound was prepared from 5-(4-{1-ethyl-1-[4-(3-ethyl-3- hydroxy-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-pentanoic acid ethyl ester. The yield was 88%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.11 (t, 6H), 1.75-1.87 (m, 8H), 2.05 (q, 4H), 2.37 (s, 3H), 2.39 (s, 3H), 2.46 (td, 2H), 3.95 (t, 2H), 6.65 (d, 1 H), 6.84 (s, 1 H), 6.91 (td, 2H), 7.00 (s, 1 H), 7.27 (d, 1 H); MS (ESI-) : 477 ([M-Kp

Example 83 Preparation of 5-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentanoic acid

(1) Preparation of 5-(4-{1 -Ethyl-1 -[3-methyl-4-(4 ,4 ,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-nnethyl- phenoxy)-pentanoic acid ethyl ester

EtO2C^^\^^. CF3 Λ_0M0M ^OMOM

Using the same procedure as described for the preparation of Example 80- (1), the title compound was prepared from 4-{1-ethyl-1-[3-methyl-4-(4,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenol (compound prepared in Example 2-(2)). The yield was 67%. 1H-NMR (300MHz, CDCI3): 7.40 (d, 1H), 7.08 (bs, 1H), 7.00 (dd, 1 H), 6.90 (dd, 1H), 6.85 (bd, 1H), 6.70 (d, 1H), 5.15 (s, 2H), 4.15 (q, 2H), 3.95 (m, 2H), 3.48 (s, 3H), 2.45-2.30 (m, 5H), 2.15 (s, 3H), 2.05 (q, 4H), 1.90-1.75 (m, 4H), 1.25 (t, 3H), 0.60 (t, 6H).

(2) Preparation of 5-(4-{1 -ethyl-1 -[3-methyl-4-(4 ,4 ,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentanoic acid ethyl ester

EtO2C^^^.o H02C^^^0. ÷ JDMOM

To a stirred solution of 5-(4-{1-ethyl-1-[3-methyl-4-(4 ,4 ,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenoxy)-pentanoic acid ethyl ester (compound prepared in Example 83-(1 )) (147 mg, 0.23 mmol) in i-PrOH (1.2 ml) was added CBr4 (7.60 mg, 10 mol%) under N2 atmosphere at room temperature and the reaction mixture was refluxed for 6.0 h. The reaction mixture was poured into water and the products were extracted with EtOAc. The extracts were washed with water and brine, dried over anhydrous Na2SO4 ,filtered and evaporated under reduced pressure. The obtained residue was purified by silica gel chromatography (n-Hexane:EtOAc=6:1 ) to give the title compound (140 mg, 86%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.40 (d, 1 H), 7.08 (bs, 1 H), 7.00 (dd, 1 H), 6.90 (dd, 1 H), 6.85 (bd, 1 H), 6.70 (d, 1 H), 4.15 (q, 2H), 3.95 (m, 3H), 2.45-2.30 (m, 5H), 2.15 (s, 3H), 2.05 (q, 4H), 1.90-1.75 (m, 4H), 1.25 (t, 3H), 0.60 (t, 6H); MS (ESI-) : 585 ([M-H∏.

(3) Preparation of 5-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentanoic acid

Using the same procedure as described for the preparation of Example 80- (2), the title compound was prepared from 5-(4-{1-ethyl-1-[3-methyl-4-(4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-pr opyl}-2-methyl- phenoxy)-pentanoic acid ethyl ester (compound prepared in Example 83- (2)). The yield was 80%. 1H-NMR(300MHz, CDCI3): 7.40 (d, 1 H), 7.08 (bs, 1 H), 7.00 (dd, 1 H), 6.90 (dd, 1 H), 6.85 (bd, 1 H), 6.70 (d, 1 H), 3.95 (m, 2H), 3.80 (m, 1 H), 2.50-2.35 (m, 5H), 2.15 (s, 3H), 2.05 (q, 4H), 1.90-1.75 (m, 4H), 0.60 (t, 6H); MS (ESI-) : 557 ([M-H]-).

Example 84 Preparation of 5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentanoic acid (1) Preparation of 5-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-nnethyl- phenoxy)-pentanoic acid ethyl ester

EtO2C^/^/^o. A OMOM ΌMOM CF3 CF3 Using the same procedure as described for the preparation of Example 80- (1 ), the title compound was prepared from 4-{1-ethyl-1-[3-methyl-4-((E)- 4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-eny l)-phenyl]- propyl}-2-methyl-phenol (compound prepared in Example 30-(1)). The yield was 84%. 1H-NMR (300MHz1 CDCI3): 0.61 (t, 6H), 1.25 (t, 3H), 1.83 (m, 4H), 2.05 (q, 4H), 2.16 (s, 3H), 2.31 (s, 3H), 2.39 (m, 2H), 3.50 (s, 3H), 3.94 (m, 2H), 4.12 (q, 2H), 4.96 (s, 2H), 6.06 (d, 1 H), 6.67 (d, 1 H), 6.88-7.03 (m, 4H), 7.35 (m, 2H).

(2) Preparation of 5-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xy)-pentanoic acid ethyl ester

EtO2C^- -x0.

Using the same procedure as described for the preparation of Example 83- (2), the title compound was prepared from 5-(4-{1-Ethyl-1-[3-methyl-4-((E)- 4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-eny l)-phenyl]- propyl}-2-methyl-phenoxy)-pentanoic acid ethyl ester (compound prepared in Example 84-(1)). The yield was 84%. 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 1.25 (t, 3H), 1.83 (m, 4H)1 2.05 (q, 4H), 2.15 (s, 3H), 2.34 (s, 3H), 2.39 (m, 2H), 3.18 (s, 1 H), 3.94 (m, 2H), 4.12 (q, 2H), 6.08 (d, 1H), 6.67 (d, 1 H), 6.87-7.03 (m, 4H), 7.35 (m, 2H).

(3) Preparation of 5-(4-{1 -ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentanoic acid

Using the same procedure as described for the preparation of Example 80- (2), the title compound was prepared from 5-(4-{1 -ethyl-1 -[3-methyl-4-((E)- 4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phen yl]-propyl}-2- methyl-phenoxy)-pentanoic acid ethyl ester (compound prepared in Example 84-(2)). The yield was 81%. 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 1.26 (t, 3H), 1.85 (m, 4H), 2.05 (q, 4H), 2.15 (s, 3H), 2.33 (s, 3H), 2.46 (m, 2H), 3.95 (m, 2H), 6.08 (d, 1 H), 6.67 (d, 1H), 6.88-7.02 (m, 3H), 7.26-7.39 (m, 3H); MS (ESI-) : 559 ([M-H]").

Example 85 Preparation of 5-(4-{1 -Ethyl-1 -[4-(1 -hydroxy-cyclopentylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid

O OH

(1) Preparation of 5-(4-{1 -ethyl-1 -[4-(1-hydroxy-cyclopentylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid ethyl ester

ho¬

using the same procedure as described for the preparation of Example 80- (1 ), the title compound was prepared from 4-{1 -ethyl-1 -[4-(1 -hydroxy- cyclopentylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 7). The yield was 84%. 1H-NMR (CDCI3): 7.27 (d, 1H)1 7.0 (s, 1H), 6.92 (m, 2H), 6.84 (dd, 1H), 6.65 (d, 1 H), 4.12 (q, 2H), 3.94 (m, 2H), 2.39 (m, 2H), 2.36 (s, 3H), 2.14 (s, 3H), 2.03 (m, 6H), 1.84 (m, 8H), 1.25 (m, 6H), 0.59 (t, 6H).

(2) Preparation of 5-(4-{1 -ethyl-1 -[4-(1-hydroxy-cyclopentylethynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid

o ^0 HO'

Using the same procedure as described for the preparation of Example 80- (2), the title compound was prepared from 5-(4-{1-ethyl-1-[4-(1-hyd roxy- cyclopentylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenox y)-pentanoic acid ethyl ester (compound prepared in Example 85-(1 )). The yield was 31%. 1H-NMR (CDCI3): 7.26 (d, 1 H), 7.0 (s, 1 H), 6.92 (m, 2H), 6.84 (dd, 1 H)1 6.65 (d, 1 H), 3.94 (m, 2H), 2.45 (m, 2H), 2.36 (s, 3H), 2.14 (s, 3H), 2.03 (m, 8H), 1.85 (m, 8H), 0.58 (t,6H); MS (ESI-) : 475 ([M-H∏.

Example 86 Preparation of 5-[4-(1 -ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanoic acid

o

(1) Preparation of 5-[4-(1 -ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanoic acid ethyl ester o OH EtO = OH

Using the same procedure as described for the preparation of Example 80- (1), the title compound was prepared from 4-(1-ethyl-1-{4-[(E)-2-(1-hydroxy- cyclopentyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenol (compound prepared in Example 10). The yield was 51 %. 1H-NMR (300MHz, CDCI3): 0.58 (t, 6H), 1.25 (t, 3H), 1.48-1.91 (m, 12H), 2.04 (q, 4H), 2.13 (s, 3H), 2.36 (s, 3H), 2.32 (t, 2H)1 3.92 (t, 2H), 4.12 (q, 2H), 6.21 (d, 1H), 6.69 (d, 1H), 6.84 (d, 1H), 6.87-7.00 (m, 4H), 7.35 (d, 1H).

(2) Preparation of 5-[4-(1-ethyl-1-{4-[(E)-2-(1-hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanoic acid

o EtO

Using the same procedure as described for the preparation of Example 80- (2), the title compound was prepared from 5-[4-(1-ethyl-1-{4-[(E)-2-(1- hydroxy-cyclopentyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methy l-phenoxy]- pentanoic acid ethyl ester (compound prepared in Example 86-(1)). The yield was 79%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.32-1.79 (m, 12H), 2.05 (q, 4H), 2.15 (s, 3H), 2.31 (s, 3H), 2.46 (t, 2H), 3.95 (t, 2H), 6.25 (d, 1H), 6.65 (d, 1 H), 6.81-6.95 (m, 5H), 7.32 (d, 1H); MS (ESI-) : 477 ([M-H]").

Example 87 Preparation of 5-(4-{1 -ethyl-1 -[4-(1-hydroxy-cyclohexylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid o

(1 ) Preparation of 5-(4-{1-ethyl-1-[4-(1-hydroxy-cyclohexylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid ethyl ester

EtO

Using the same procedure as described for the preparation of Example 80- (1 ), the title compound was prepared from 4-{1-ethyl-1-[4-(1-hydroxy- cyclohexylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 8). The yield was 51 %. 1H-NMR (300MHz1 CDCI3): 0.59 (t, 6H), 1.25 (t, 3H), 1.52-1.79 (m, 8H), 1.85 (q, 4H), 2.03 (m, 6H), 2.15 (s, 3H), 2.38 (s, 3H), 2.38 (t, 2H), 3.95 (t, 2H), 6.66 (d, 1 H), 6.84 (s, 1H), 6.92 (td, 2H), 7.00 (s, 1 H), 7.27 (d, 1 H).

(2) Preparation of 5-(4-{1-ethyl-1-[4-(1-hydroxy-cyclohexylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid

EtO HO

Using the same procedure as described for the preparation of Example 80- (2), the title compound was prepared from 5-(4-{1-Ethyl-1-[4-(1-hydroxy- cyclohexylethynyO-S-methyl-phenyll-propylJ^-methyl-phenoxyJ- pentanoic acid ethyl ester (compound prepared in Example 87-(1)). The yield was 80%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.25 (m, 1 H), 1.52-1.79 (m, 7H), 1.85 (m, 4H), 2.03 (q, 6H), 2.14 (s, 3H), 2.38 (s, 3H), 2.46 (t, 2H), 3.95 (t, 2H), 6.66 (d, 1 H), 6.84 (s, 1 H), 6.92 (td, 2H), 7.00 (s, 1 H), 7.27 (d, 1 H) ; MS (ESI-) : 489 ([M-H]'). Example 88 Preparation of 5-[4-(1 -ethyl-1-{4-[(E)-2-(1 -hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanoic acid

o

(1) Preparation of 5-[4-(1-ethyl-1-{4-[(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanoic acid ethyl ester

o OH EtO

Using the same procedure as described for the preparation of Example 80- (1 ), the title compound was prepared from 4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy- cyclohexyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenol (compound prepared in Example 11). The yield was 64%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.25 (t, 3H), 1.31-1.79 (m, 10H), 1.85 (m, 4H), 2.03 (q, 4H), 2.14 (s, 3H), 2.38 (s, 3H), 2.38 (t, 2H), 3.99 (t, 2H), 4.18 (q, 2H), 6.21 (d, 1 H), 6.69 (d, 1 H), 6.84 (d, 1 H), 6.87-7.00 (m, 4H), 7.35 (d, 1 H).

(2) Preparation of 5-[4-(1 -ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanoic acid

o EtO

Using the same procedure as described for the preparation of Example 80- (2), the title compound was prepared from 5-[4-(1 -ethyl-1 -{4-[(E)-2-(1- hydroxy-cyclohexyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methyl -phenoxy]- pentanoic acid ethyl ester (compound prepared in Example 88-(1)). The yield was 83%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.32 (m, 1 H), 1.52-1.79 (m, 9H), 1.85 (m, 4H), 2.03 (q, 4H), 2.14 (s, 3H), 2.38 (s, 3H), 2.46 (t, 2H), 3.95 (t, 2H), 6.20 (d, 1H), 6.69 (d, 1H), 6.81 (d, 1H), 6.87-7.00 (m, 4H), 7.31 (d, 1H) ; MS (ESI-) : 491 ([M-H]').

Example 89 Preparation of 6-(4-{1 -ethyl- 1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid

o

(1 ) Preparation of 6-(4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid ethyl ester

EtO. OH OH

Using the same procedure as described for the preparation of Example 80- (1), the title compound was prepared from 4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy- pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(4)) and ethyl-6-bromohexanoate. The yield was 64%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.11 (t, 6H), 1.25 (t, 3H), 1.44-1.57 (m, 2H), 1.64-1.85 (m, 8H), 1.98-2.07 (m, 4H), 2.14 (s, 3H), 2.33 (t, 2H), 2.37 (s,3H), 3.92 (t, 2H), 4.13 (q, 2H), 6.60 (d, 1 H, J=8.4 Hz), 6.83-6.95 (m, 3H), 7.00 (s, 1 H), 7.27 (d, 1 H, J=8.0 Hz).

(2) Preparation of 6-(4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid

EtO Using the same procedure as described for the preparation of Example 80- (2), the title compound was prepared from 6-(4-{1 -ethyl-1 -[4-(3-ethyl-3- hydroxy-pent-1-ynyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-hexanoic acid ethyl ester (compound prepared in Example 89-(1 )). The yield was 85%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.11 (t, 6H), 1.49-1.59 (m, 2H), 1.67-1.85 (m, 8H), 2.03 (q, 4H), 2.14 (s, 3H), 2.36-2.42 (m, 5H), 3.92 (t, 2H), 6.66 (d, 1H, J=8.4 Hz), 6.84-6.95 (m, 3H), 7.00 (s, 1H), 7.26 (d, 1H, J=8.0 Hz); MS (ESI-) : 491 ([M-H]").

Example 90 Preparation of 6-(4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid

o

(1) Preparation of 6-(4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid ethyl ester

EtO,

Using the same procedure as described for the preparation of Example 80- (1), the title compound was prepared from 4-{1 -ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno l (compound prepared in Example 1-(5)) and ethyl-6-bromohexanoate. The yield was 75%. 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 0.91 (t, 6H),1.25 (t, 3H), 1.47-1.85 (m, 10H), 2.05 (q, 4H), 2.15 (s,3H), 2.30 (s,3H), 2.39 (t, 2H), 3.95 (t 2H), 4.13 (q, 2H), 6.00 (d, 1 H, J= 16.0 Hz), 6.66 (d, 1 H, J= 8.4 Hz), 6.74 (d, 1 H, J= 16.0 Hz), 6.90-6.96 (m, 4H), 7.29 (d, 1H, J= 8.7 Hz). (2) Preparation of 6-(4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid

Using the same procedure as described for the preparation of Example 80- (2), the title compound was prepared from 6-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-hexanoic acid ethyl ester (compound prepared in Example 90-(1)). The yield was 75%. 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 0.91 (t, 6H), 1.49-1.85 (m, 10H), 2.04 (q, 4H), 2.15 (s,3H), 2.30 (s,3H), 2.39 (t, 2H), 3.93 (t 2H), 6.00 (d, 1 H, J = 16.0 Hz), 6.66 (d, 1 H, J = 8.4 Hz), 6.74 (d, 1 H, J = 16.0 Hz), 6.90-6.96 (m, 4H), 7.29 (d, 1H, J=8.7 Hz); MS (ESI-) : 493 ([M-H]").

Example 91 Preparation of 6-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl-phenoxy)-hexanoic acid

o

(1) Preparation of 6-(4-{1 -ethyl-1 -[3-methyl-4-(4,4 ,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenoxy)-hexanoic acid ethyl ester

,, OMOM CF3 ,,_OMOM CF3 Using the same procedure as described for the preparation of Example 80- (1), the title compound was prepared from 4-{1-ethyl-1-[3-methyl-4-(4 ,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenol (compound prepared in Example 2-(2))and ethyl-6- bromohexanoate. The yield was 80%. 1H-NMR (300MHz, CDCI3): 7.40 (d, 1 H), 7.08 (bs, 1 H), 7.00 (dd, 1H), 6.90 (dd, 1 H), 6.85 (bd, 1 H), 6.70 (d, 1 H), 5.15 (s, 2H), 4.15 (q, 2H), 3.95 (m, 2H), 3.48 (s, 3H), 2.45-2.30 (m, 5H), 2.15 (s, 3H), 2.05 (q, 4H), 1.90-1.65 (m, 4H), 1.60-1.45 (m, 2H), 1.25 (t, 3H), 0.60 (t, 6H).

(2) Preparation of 6-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-hexanoic acid ethyl ester

EtO2' CF3 ^pOMOM

Using the same procedure as described for the preparation of Example 83- (2), the title compound was prepared from 6-(4-{1 -ethyl- 1-[3-methyl-4-(4, 4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenoxy)-hexanoic acid ethyl ester (compound prepared in Example 91 -(1)). The yield was 90%. 1H-NMR (300MHz, CDCI3): 7.40 (d, 1 H), 7.08 (bs, 1 H), 7.00 (dd, 1 H), 6.90 (dd, 1H), 6.85 (bd, 1H), 6.70 (d, 1H), 4.15 (q, 2H), 3.95 (m, 3H), 2.45-2.30 (m, 5H), 2.15 (s, 3H), 2.05 (q, 4H), 1.90-1.75 (m, 4H), 1.30-1.20 (m, 5H), 0.60 (t, 6H).

(3) Preparation of 6-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl-phenoxy)-hexanoic acid Using the same procedure as described for the preparation of Example 80- (2), the title compound was prepared from 6-(4-{1-ethyl-1-[3-methyl-4-(4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-pr opyl}-2-methyl- phenoxy)-hexanoic acid ethyl ester (compound prepared in Example 91 -(2)). The yield was 72%. 1H-NMR (300MHz, CDCI3): 7.40 (d, 1H), 7.08 (bs, 1 H), 7.00 (dd, 1 H), 6.90 (dd, 1 H), 6.85 (bd, 1 H), 6.70 (d, 1 H), 3.95 (m, 2H), 3.80 (m, 1 H), 2.50-2.35 (m, 5H), 2.15 (s, 3H), 2.05 (q, 4H), 1.90-1.70 (m, 4H), 1.65-1.50 (m, 2H), 0.60 (t, 6H); MS (ESI") : 571 ([M-H]").

Example 92 Preparation of 6-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-hexanoic acid

(1 ) Preparation of 6-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxy)-hexanoic acid ethyl ester

r-PMOM EtO2C^^\^O' , i - £θMOM

To a stirred solution of 4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenol (compound prepared in Example 30-(1)) (143 mg, 0.28 mmol) and ethyl-6-bromohexanoate (0.15 ml, 0.85 mmol) in anhydrous DMF (1.4 ml) was added K2CO3 (116 mg, 0.84 mmol) under N2 atmosphere at room temperature and the mixture was stirred at 110 degrees C for 5 h. The reaction mixture was poured into water and the products were extracted with AcOEt. The extracts were washed with water and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane:EtOAc (5:1 ) to give the title compound (160 mg, 88%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.50 (m, 2H), 7.15 (m, 2H), 7.00-6.85 (m, 2H), 6.70 (d, 1 H), 6.08 (d, 1H), 4.98 (s, 2H), 4.15 (q, 2H), 3.95 (t, 2H), 3.50 (s, > 3H), 2.40-2.35 (m, 6H), 2.15-2.00 (m, 4H), 1.90-1.50 (m, 8H), 1.25 (t, 3H), 0.60 (t, 6H).

(2) Preparation of 6-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3 - trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-hexanoic acid ethyl ester

EtO2C

To a stirred solution of 6-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxy)-hexanoic acid ethyl ester (compound prepared in Example 92-(1 )) (160 mg, 0.25 mmol) in of EtOH (2.0 ml) was added CBr4 (13.6 mg, 10 mol%) under N2 atmosphere at room temperature and the mixture was stirred at reflux temperature for 2.5 h. The reaction mixture was cooled to room temperature, poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :10) to give the title compound (122 mg, 73%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.35 (m, 2H), 7.05 (m, 2H), 6.95-6.85 (m, 2H), 6.68 (d, 1 H), 6.10 (d, 1H), 4.15 (q, 2H), 3.95 (t, 2H), 3.20 (bs, 1 H), 2.40-2.30 (m, 5H), 2.15 (s, 3H), 2.05 (q, 4H), 1.85-1.65 (m, 4H), 1.60-1.45 (m, 2H), 1.25 (t, 3H), 0.60 (t, 6H).

(3) Preparation of 6-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3 - trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-hexanoic acid EtOaC^^-^-^O- HO2C

To a stirred solution of 6-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-meth yl-phenoxy)- hexanoic acid ethyl ester (compound prepared in Example 92-(2)) (122 mg, 0.20 mmol) in EtOH/Water (4/1 v/v, 2.5 ml) was added KOH (23.0 mg, 0.41 mmol) and the mixture was stirred at room temperature for 4 h. The reaction mixture was poured into 0.1 N HCI and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :2) to give the title compound (90 mg, 78%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.35 (m, 2H), 7.05 (m, 2H), 6.95-6.85 (m, 2H), 6.68 (d, 1 H), 6.10 (d, 1H), 3.95 (t, 2H), 2.40-2.30 (m, 5H), 2.15 (s, 3H), 2.05 (q, 4H), 1.85-1.65 (m, 4H), 1.60-1.45 (m, 2H), 0.60 (t, 6H); MS (ESP) : 573 ([M-H]-).

Example 93 Preparation of 6-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid

HOOC

(1 ) Preparation of 6-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid ethyl ester

EtOOC^^^^^^O' OH ' ' OH To a solution of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 18) (200 mg, 0.52 mmol) in DMF (5 ml) were added K2CO3 (144 mg, 1.04 mmol) and 6-bromohexanoic acid ethyl ester (0.184 ml, 1.04 mmol) and the mixture was stirred at 50 degrees C for 13 h. The reaction mixture was cooled to room temperature, poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :10) to give the title compound (214 mg, 78%). 1H-NMR (300MHz, CDCI3): 0.6 (t, 6H), 0.89 (s, 9H), 1.29 (m, 3H), 1.52 (m, 3H), 1.81 (m, 5H), 2.05 (q, 4H), 2.16 (s,3H), 2.26 (s,3H), 2.35 (t, 2H), 2.56 (m, 1 H), 2.85 (m, 1 H), 3.26 (m, 1H), 3.92 (t, 2H), 4.12 (q, 2H), 6.66 (d, 1 H), 6.90 (m, 4H), 7.02 (d, 1 H).

(2) Preparation of 6-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid

' ' OH i I OH To a stirred solution of 6-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid ethyl ester (compound prepared in Example 93-(1)) (214 mg, 0.408 mmol) in MeOH (3 ml) was added 1 N-KOH (1.22 ml, 1.22 mmol) and the mixture was stirred at room temperature for 5 h. The reaction mixture was poured into 1 N-HCI and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n- Hexane (1 :3) to give the title compound (144 mg, 71%). 1H-NMR (300MHz, CDCI3): 0.6 (t, 6H), 0.89 (s, 9H), 1.52 (m, 3H), 1.81 (m, 5H), 2.05 (q, 4H), 2.16 (s,3H), 2.26 (s,3H), 2.39 (t, 2H), 2.56 (m, 1 H), 2.85 (m, 1 H), 3.26 (m, 1H), 3.92 (t, 2H), 6.66 (d, 1H), 6.90 (m, 4H), 7.02 (d, 1 H); MS (ESP) : 495 ([M-H]").

Example 94 Preparation of 6-(4-{1 -ethyl-1 -[4-(1 -hydroxy-cyclopentylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid

HO == OH O

(1) Preparation of 6-(4-{1 -ethyl-1 -[4-(1-hydroxy-cyclopentylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid ethyl ester

EtO o

To a solution of 4-{1 -ethyl-1 -[4-(1-hydroxy-cyclopentylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 7) (114 mg, 0.303 mmol) in DMF (5 ml) were added K2CO3 (126 mg, 0.908 mmol) and 6-bromo-hexanoic acid ethyl ester (135 mg, 0.606 mmol) and the mixture was stirred at 90 degrees C for 6 h. The reaction mixture was cooled to room temperature, poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :6) to give the title compound (71 mg, 45%). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.25 (t, 3H), 1.31-1.79 (m, 10H), 1.85 (m, 4H), 2.03 (q, 4H), 2.14 (s, 3H), 2.30 (t, 2H), 2.36 (s, 3H), 3.99 (t, 2H), 4.18 (q, 2H), 6.68 (d, 1 H), 6.84 (m, 2H), 6.91 (d, 1 H), 7.00 (s, 1H), 7.27 (d, 1 H).

(2) Preparation of 6-(4-{1-ethyl-1-[4-(1-hydroxy-cyclopentylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid

EtO To a stirred solution of 6-(4-{1 -ethyl-1 -[4-(1-hydroxy-cyclopentylethynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid ethyl ester (compound prepared in Example 94-(1)) (71 mg, 0.137 mmol) in MeOH (1.4 ml) was added 1 N-KOH (0.41 ml, 0.411 mmol) and the mixture was stirred at room temperature for 18 h. The reaction mixture was poured into 1 N-HCI and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :2) to give the title compound (56.6 mg, 84%). 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.32-1.79 (m, 14H), 2.03 (q, 4H), 2.14 (s, 3H), 2.37 (s, 3H), 2.40 (t, 2H), 3.91 (t, 2H), 6.68 (d, 1 H), 6.84 (m, 2H), 6.91 (d, 1 H), 7.00 (s, 1H), 7.27 (d, 1H); MS (ESI-) : 489 ([M-H∏.

Example 95 Preparation of 6-[4-(1 -ethyl-1-{4-[(E)-2-(1 -hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-hexanoic acid

HO o

(1) Preparation of 6-[4-(1-ethyl-1-{4-[(E)-2-(1 -hyd roxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-hexanoic acid ethyl ester

OH EtO O

To a solution of 4-(1 -ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenol (compound prepared in Example 10) (110 mg, 0.291 mmol) in DMF (5 ml) were added K2CO3 (120 mg, 0.872 mmol) and 6-bromo-hexanoic acid ethyl ester (130 mg, 0.582 mmol) and the mixture was stirred at 90 degrees C for 6 h. The reaction mixture was cooled to room temperature, poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :7) to give the title compound (73 mg, 48%). 1H-NMR (300MHz, CDCI3): 0.58 (t, 6H), 1.25 (t, 3H), 1.39-1.88 (m, 14H), 2.03 (q, 4H), 2.13 (s, 3H), 2.30 (t, 2H), 2.38 (s, 3H), 3.92 (t, 2H), 4.12 (q, 2H), 6.21 (d, 1H), 6.69 (d, 1 H), 6.84 (d, 1H), 6.87-7.00 (m, 4H), 7.35 (d, 1H).

(2) Preparation of 6-[4-(1-ethyl-1-{4-[(E)-2-(1-hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-hexanoic acid

EtO

To a stirred solution of 6-[4-(1-ethyl-1-{4-[(E)-2-(1-hydroxy-cyclopentyl)- vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-hexanoic acid ethyl ester (compound prepared in Example 95-(1)) (73 mg, 0.140 mmol) in MeOH (1.4 ml) was added 1 N-KOH (0.42 ml, 0.420 mmol) and the mixture was stirred at room temperature for 18 h. The reaction mixture was poured into 1 N-HCI and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :2) to give the title compound (60 mg, 87%). 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.32-1.79 (m, 14H), 2.03 (q, 4H), 2.14 (s, 3H), 2.31 (s, 3H), 2.40 (t, 2H), 3.93 (t, 2H), 6.25 (d, 1 H), 6.65 (d, 1 H), 6.81-6.96 (m, 5H), 7.31 (d, 1 H); MS(ESI-) : 491([M-H]-).

Example 96 Preparation of 6-(4-{1 -ethyl-1 -[4-(1 -hydroxy-cyclohexylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid (1) Preparation of 6-(4-{1-ethyl-1-[4-(1-hydroxy-cyclohexylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid ethyl ester

EtO.

To a solution of 4-{1-ethyl-1-[4-(1-hydroxy-cyclohexylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 8) (110 mg, 0.28 mmol) in DMF (3 ml) were added K2CO3 (116 mg, 0.84 mmol) and 6-bromo-hexanoic acid ethyl ester (0.1 ml, 0.56 mmol) and the mixture was stirred at 90 degrees C for 13 h. The reaction mixture was cooled to room temperature, poured into saturated NH4CI aq. and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :6) to give the title compound (133 mg, 89%). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.25 (t, 3H), 1.49-1.82 (m, 16H), 2.03 (q, 4H), 2.14 (s, 3H), 2.33 (t, 2H), 2.38 (s, 3H), 3.92 (t, 2H), 4.12 (q, 2H), 6.66 (d, 1 H), 6.84-7.01 (m, 4H), 7.27 (d, 1 H).

(2) Preparation of 6-(4-{1-ethyl-1-[4-(1-hydroxy-cyclohexylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid

EtO.

To a stirred solution of 6-(4-{1-ethyl-1-[4-(1-hydroxy-cyclohexylethynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexanoic acid ethyl ester (compound prepared in Example 96-(1)) (133 mg, 0.25 mmol) in MeOH (2 ml) was added 1 N-KOH (0.75 ml, 0.75 mmol) and the mixture was stirred at room temperature for 13 h. The reaction mixture was poured into saturated NH4CI aq. and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :2) to give the title compound (95 mg, 75%). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.43-1.82 (m, 16H), 2.03 (q, 4H), 2.14 (s, 3H), 2.38 (s, 3H), 2.40 (t, 2H), 3.93 (t, 2H), 6.66 (d, 1 H), 6.84-7.01 (m, 4H), 7.27 (d, 1 H); MS (ESI-) : 503 ([M-H]").

Example 97 Preparation of 6-[4-(1 -ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-hexanoic acid

o

(1 ) Preparation of 6-[4-(1 -ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-hexanoic acid ethyl ester

EtO O

To a solution of 4-(1 -ethyl-1 -{4-[(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenol (compound prepared in Example 11 ) (96.6 mg, 0.246 mmol) in DMF (3 ml) were added K2CO3 (102 mg, 0.738 mmol) and 6-bromo-hexanoic acid ethyl ester (110 mg, 0.492 mmol) and the mixture was stirred at 90 degrees C for 12 h. The reaction mixture was cooled to room temperature, poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :6) to give the title compound (112 mg, 85%). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.25 (t, 3H), 1.31-1.79 (m, 12H), 1.85 (m, 4H), 2.03 (q, 4H), 2.14 (s, 3H), 2.30 (s, 3H), 2.38 (t, 2H)1 3.92 (t, 2H), 4.3 (q, 2H), 6.19 (d, 1 H), 6.65 (d, 1 H), 6.82 (d, 1 H), 6.89-7.00 (m, 4H), 7.32 (d, 1 H) ; MS (ESI+) : 557 ([M+Na]+). (2) Preparation of 6-[4-(1 -ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-hexanoic acid

EtO

To a stirred solution of 6-[4-(1 -ethyl-1 -{4-[(E)-2-(1 -hydroxy-cyclohexyl)- vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-hexanoic acid ethyl ester (compound prepared in Example 97-(1)) (112 mg, 0.209 mmol) in MeOH (2.1 ml) was added 1 N-KOH (0.63 ml, 0.63 mmol) and the mixture was stirred at room temperature for 12 h. The reaction mixture was poured into saturated NH4CI aq. and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :2) to give the title compound (76 mg, 71%). 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.32-1.79 (m, 16H), 2.03 (q, 4H), 2.14 (s, 3H), 2.30 (s, 3H), 2.40 (t, 2H), 3.93 (t, 2H), 6.19 (d, 1 H), 6.65 (d, 1 H), 6.80 (d, 1 H), 6.9-6.95 (m, 4H), 7.30 (d, 1 H); MS (ESI-) : 505 ([M-H∏.

Example 98 Preparation of 7-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-heptanoic acid

HO2C

(1 ) Preparation of 7-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-heptanoic acid ethyl ester To a solution of 4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 18) (200 mg, 0.52 mmol) in DMF (5 ml) were added K2CO3 (144 mg, 1.04 mmol) and 7-bromoheptanoic acid ethyl ester (0.202 ml, 1.04 mmol) and the mixture was stirred at 50 degrees C for 13 h. The reaction mixture was cooled to room temperature, poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :10) to give the title compound (231 mg, 83%). 1H-NMR (300MHz, CDCI3): 0.6 (t, 6H)1 0.89 (s, 9H), 1.29 (m, 3H), 1.45 (m, 5H), 1.69 (m, 2H), 1.81 (m, 3H), 2.05 (q, 4H), 2.16 (s,3H), 2.26 (s,3H), 2.31 (t, 2H), 2.56 (m, 1H), 2.85 (m, 1H), 3.26 (m, 1H), 3.92 (t, 2H), 4.12 (q, 2H), 6.66 (d, 1H), 6.90 (m, 4H), 7.02 (d, 1H).

(2) Preparation of 7-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-heptanoic acid

OH To a stirred solution of 7-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-heptanoic acid ethyl ester (compound prepared in Example 98-(1)) (231 mg, 0.429 mmol) in MeOH (3 ml) was added 1 N-KOH (1.29 ml, 1.29 mmol) and the mixture was stirred at room temperature for 5 h. The reaction mixture was poured into 1 N-HCI and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n- Hexane (1 :3) to give the title compound (153 mg, 70%). 1H-NMR (300MHz, CDCI3): 0.6 (t, 6H), 0.89 (s, 9H), 1.45 (m, 5H), 1.69 (m, 2H), 1.81 (m, 3H), 2.05 (q, 4H), 2.16 (s,3H), 2.26 (s,3H), 2.38 (t, 2H), 2.56 (m, 1 H), 2.85 (m, 1 H), 3.26 (m, 1 H), 3.91 (t, 2H), 6.66 (d, 1 H), 6.90 (m, 4H), 7.02 (d, 1 H); MS (ESI-) : 509 ([M-H∏.

Example 99 Preparation of 1 -(4-{1 -[4-(2-amino-ethoxy)-3-methyl-phenyl]-1 -ethyl-propyl}- 2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol

H2N^^, O'

Preparation of 1 -(4-{1 -[4-(2-amino-ethoxy)-3-methyl-phenyl]-1 -ethyl-propyl}- 2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol

To a solution of 4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 18) (100 mg, 0.261 mmol) in THF-DMF(5:1 , 0.45 ml) was added NaH (46 mg, 1.17 mmol) at 0 degrees C and the mixture was stirred at room temperature for 15 min. Then bromoethylamine HBr salt (79 mg, 0.391 mmol) was added and the mixture was stirred at 55 degrees C for 1.5 h. The reaction mixture was cooled to 0 degrees C, neutralized to pH7 with sat. NH4CI aq. The reaction mixture was poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on amino functionalized silica gel with EtOAc-n-Hexane (3:1) to give the title compound (55 mg, 50%). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.43-1.57 (m, 1 H), 1.74-1.84 (m, 1H), 2.03 (q, 4H), 2.17(s, 3H), 2.25 (s, 3H), 2.50-2.60 (m, 1 H)1 2.81-2.91 (m, 1 H), 3.07 (t, 2H), 3.24 (d, 1 H), 3.96 (t, 2H), 6.68 (d, 1 H), 6.90- 6.96 (m, 4H), 7.01 (d, 1 H); MS (ESI+) : 426 ([M+H∏. Example 100 Preparation of 1 -(4-{1 -[4-(3-amino-propoxy)-3-methyl-phenyl]-1-ethyl-propyl}- 2-methyl-phenyl)-4,4-dimethyl-pentan~3-ol

H7N

(1 ) Preparation of 2-[3-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propyl]-isoindole-1 ,3-dione

To a solution of 4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 18) (340 mg, 0.915 mmol) in acetonitrile (9 ml) were added K2CO3 (253 mg, 1.83 mmol) and N-(3-bromopropyl)phthalimide (491 mg, 1.83 mmol) and the mixture was stirred at reflux temperature for 5 h. The reaction mixture was cooled to room temperature, concentrated under reduced pressure. The residue was diluted with EtOAc and washed with water and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :6) to give the title compound (460 mg, 88%). 1H-NMR (300MHz, CDCI3): 0.58 (t, 6H), 0.89 (s, 9H), 1.37 (d, 1H), 1.42-1.53 (m, 1 H), 1.78-1.84 (m,1 H), 2.04 (q, 4H), 2.11(s, 3H), 2.14-2.21 (m, 2H), 2.25 (s, 3H), 2.50-2.60 (m, 1 H), 2.77-2.92 (m, 1 H), 3.21-3.27 (dd, 1 H), 3.91 (t, 2H), 4.00 (t, 2H), 6.66 (d, 1H), 6.88-6.92 (m, 4H), 7.00 (d, 1 H), 7.68-7.71 (m, 2H), 7.82-7.85 (m, 2H); MS (ESI+) : 587 ([M+NH4]+).

(2) Preparation of 1-(4-{1-[4-(3-amino-propoxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol H2N^^^O-

To a solution of 2-[3-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propyl]-isoindole-1 ,3-clione (compound prepared in Example 100-(1)) (460 mg, 0.807 mmol) in EtOH (6 ml) was added hydrazine hydrate(0.4 ml, 8.07 mmol) and the mixture was stirred at reflux temperature for 1 h. The reaction mixture was cooled to room temperature, concentrated under reduced pressure. The obtained residue was diluted with EtOAc, and filtered. The filtrate was concentrated, and purified by amino functional ized silica gel chromatography (EtOAc-n- Hexane=1:1 to EtOAc) to give the title compound (264 mg, 74%). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.43-1.57 (m, 1 H), 1.74-1.84 (m, 1 H), 1.92 (q, 2H), 2.03 (q, 4H), 2.15 (s, 3H), 2.25 (s, 3H), 2.49- 2.62 (m, 1H), 2.81-2.89 (m, 1H), 2.92 (t, 2H), 3.23 (dd, 1H), 4.01 (t, 2H), 6.68 (d, 1 H), 6.90-6.96 (m, 4H), 7.01 (d, 1 H); MS (ESI+) : 440 ([M+H]+).

Example 101 Preparation of 1 -(4-{1 -[4-(4-amino-butoxy)-3-methyl-phenyl]-1 -ethyl-propyl}- 2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol

H7N

(1) Preparation of 2-[4-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-butyl]-isoindole-1 ,3-dione

Using the same procedure as described for the preparation of Example 100-(1), the title compound was prepared from 4-{1-Ethyl-1-[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno l (compound prepared in Example 18) and N-(4-bromobutyl)phthalimide. The yield was 97%. 1H-NMR (300MHz, CDCI3): 0.58 (t, 6H), 0.88 (s, 9H), 1.39 (d, 1 H), 1.44-1.55 (m, 1 H), 1.74-1.96 (m, 5H), 2.03 (q, 4H), 2.14 (s, 3H), 2.25 (s, 3H), 2.49-2.62 (m, 1 H), 2.79-2.92 (m, 1 H), 3.23 (dd, 1 H), 3.77 (t, 2H), 3.96 (t, 2H), 6.64 (d, 1 H), 6.87-6.95 (m, 4H), 7.00 (d, 1 H), 7.65-7.75 (m, 2H), 7.78-7.87 (m, 2H); MS (ESI+) : 601 ([M+NH4]+).

(2) Preparation of 1-(4-{1-[4-(4-amino-butoxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol

Using the same procedure as described for the preparation of Example 100-(2), the title compound was prepared from 2-[4-(4-{1-ethyl-1-[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)- butyl]-isoindole-1 ,3-dione (compound prepared in Example 101-(1)). The yield was 87%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.44-1.59 (m, 1 H), 1.59-1.70 (m, 2H), 1.72-1.88 (m, 3H), 2.03 (q, 4H), 2.15 (s, 3H), 2.25 (s, 3H), 2.48-2.62 (m, 1 H), 2.75 (t, 2H), 2.80-2.92 (m, 1 H), 3.24 (dd, 1 H), 3.94 (t, 2H), 6.64 (d, 1 H), 6.88-6.96 (m, 4H), 7.01 (d, 1 H); MS (ESI+) : 454 ([M+H]+).

Example 102 Preparation of 1 -(4-{1 -[4-(5-amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl- propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol

H2N'

(1 preparation of 2-[5-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentyl]-isoindole-1 ,3-dione Using the same procedure as described for the preparation of Example 100-(1), the title compound was prepared from 4-{1-ethyl-1-[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno l (compound prepared in Example 18) and N-(5-bromopentyl)phthalimide. The yield was 99%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.38 (d, 1H), 1.45-1.58 (m, 3H), 1.71-1.87 (m, 5H), 2.06 (q, 4H), 2.11 (s, 3H), 2.25 (s, 3H), 2.50-2.61 (m, 1 H), 2.80-2.90 (m, 1 H), 3.24 (dd, 1H), 3.72 (t, 2H), 3.91 (t, 2H), 6.64 (d, 1 H), 6.85-6.95 (m, 4H), 7.01 (d, 1H), 7.66-7.72 (m, 2H), 7.78-7.88 (m, 2H); MS (ESI+) : 615 ([M+NH4]+).

(2) Preparation of 1-(4-{1-[4-(5-amino-pentyloxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol

Using the same procedure as described for the preparation of Example 100-(2), the title compound was prepared from 2-[5-(4-{1 -ethyl-1 -[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)- pentyl]-isoindole-1 ,3-dione (compound prepared in Example 102-(1)). The yield was 87%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.45-1.56 (m, 5H), 1.74-1.84 (m, 3H), 2.03 (q, 4H), 2.15 (s, 3H), 2.25 (s, 3H), 2.50-2.60 (m, 1 H), 2.72 (t, 2H), 2.80-2.90 (m, 1 H), 3.24 (dd, 1 H), 3.92 (t, 2H), 6.67 (d, 1 H), 6.85-6.96 (m, 4H), 7.02 (d, 1 H); MS (ESI+) : 468 ([M+H]+).

Example 103 Preparation of 1 -(4-{1 -[4-(6-amino-hexyloxy)-3-m8thyl-phenyl]-1 -ethyl- propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol

(1 ) Preparation of 2-[6-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexyl]-isoindole-1 ,3-dione

HO'

Using the same procedure as described for the preparation of Example 100-(1), the title compound was prepared from 4-{1-ethyl-1-[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno l (compound prepared in Example 18) and N-(6-bromohexyl)phthalimide. The yield was 99%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.36-1.56 (m, 5H), 1.65-1.85 (m, 5H), 2.03 (q, 4H), 2.13 (s, 3H), 2.25 (s, 3H), 2.50-2.60 (m, 1H), 2.81-2.90 (m, 1H), 3.24 (dd, 1 H), 3.69 (t, 2H), 3.90 (t, 2H), 6.65 (d, 1 H), 6.89- 6.93 (m, 4H), 7.01 (d, 1H), 7.65-7.74 (m, 2H), 7.78-7.87 (m, 2H); MS (ESI+) : 629 ([M+NH4]+).

(2) Preparation of 1-(4-{1-[4-(6-Amino-hexyloxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol

Using the same procedure as described for the preparation of Example 100-(2), the title compound was prepared from 2-[6-(4-{1-ethyl-1-[4-(3- hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-meth yl-phenoxy)- hexyl]-isoindole-1 ,3-dione (compound prepared in Example 103-(1)). The yield was 60%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H)1 0.89 (s, 9H), 1.35-1.56 (m, 7H), 1.74-1.84 (m, 3H), 2.03 (q, 4H)1 2.15 (s, 3H), 2.25 (s, 3H), 2.50-2.60 (m, 1 H), 2.70 (t, 2H), 2.81-2.91 (m, 1 H), 3.24 (dd, 1 H), 3.92 (t, 2H), 6.67 (d, 1 H), 6.90- 6.95 (m, 4H), 7.01 (d, 1H); MS (ESI+) : 482 ([M+H]+).

Example 104 Preparation of 3-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenyl)-propionic acid

(1 ) Preparation of 3-ethyl-1 -trimethylsilanyl-pent-1 -yn-3-ol == — TMS *- TMS — -≡ ^OH To a solution of TMS-acetylene (1.55g, 15.78mmol) in THF (20 ml) under nitrogen atmosphere at -40 degrees C were added n-BuLi (7.5 mL, 18.93mmol, 2.5M in hexane) and 3-pentanone (2.0 mL, 18.93 mmol) and the mixture was stirred for 3 h. The reaction mixture was diluted with diethyl ether, washed with sat. NH4CI aq., water and brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :15) to give the title compound (2.8 g, 96%). 1H NMR (CDCI3): 1.86 (br, OH), 1.65 (m, 4H), 1.02 (t, 6H), 0.16 (s, 9H).

(2) Preparation of 3-ethyl-pent-1 -yn-3-ol TMS-^≡ — ^OH -

To a solution of 3-ethyl-1 -trimethylsilanyl-pent-1 -yn-3-ol (compound prepared in Example 104-(1)) (920 mg, 4.99 mmol) in diethyl ether (10 ml) under nitrogen atmosphere at 0 degrees C was added TBAF (7.48mL, 7.48mmol, 1.0M in THF) and the mixture was stirred for 2 h. The reaction mixture was diluted with diethyl ether, and washed with sat. NH4CI aq., H2O and brine, and dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :10) to give the title compound (200 mg, 35%). 1H NMR (CDCI3): 2.43 (s, 1H), 1.88 (br, OH), 1.69 (m, 4H), 1.04 (t, 6H).

(3) Preparation of 3-{4-[1-ethyl-1-(3-methyl-4-trifluoromethanesulfonyloxy- phenyl)-propyl]-2-methyl-phenyl}-propionic acid methyl ester

.OCH, OCH3 TfO O 1 1 O To a solution of 3-{4-[1-ethyl-1-(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenyl}-propionic acid methyl ester (compound prepared in Example 18-(2)) (1.81 g, 5.1 mmol) in anhydrous CH2CI2 (30 ml) under nitrogen atmosphere at room temperature were added trifluoromethanesulfonic anhydride (1.3 ml, 7.65 mmol) and pyridine (1.3 ml, 15.3 mmol). After stirring 1.5 h at room temperature, the mixture was poured into sat. NH4CI aq. and the products were extracted with CH2CI2. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on amino functionalized silica gel with EtOAc-n-Hexane (1 :10) to give the title compound (2.0 g, 80%). 1H NMR (CDCI3): 7.11-6.99 (m, 4H), 6.88 (m, 2H), 3.67 (s, 3H), 2.90 (dt, 2H), 2.58 (dt, 2H), 2.31 (s, 3H), 2.26 (s, 3H), 2.04 (q, 4H), 0.59 (t, 6H).

(4) Preparation of 3-(4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenyl)-propionic acid methyl ester

H3CO. H3CO. OTf

To a solution of 3-{4-[1-ethyl-1-(3-methyl-4-trifluoromethanesulfonyloxy- phenyl)-propyl]-2-methyl-phenyl}-propionic acid methyl ester (compound prepared in Example 104-(3)) (100mg, 0.2mmol) in anhydrous CH3CN (2m) under nitrogen atmosphere were added Pd(PPh3)4 (46 mg, 0.04 mmol), CuI (7.6 mg, 0.04 mmol), triethylamine (0.083 ml, 0.6 mmol) and 3-ethyl-pent-1- yn-3-ol (compound prepared in Example 104-(2)) (200 mg, 1.78 mmol). After stirring overnight at 100 degrees C, the mixture was poured into sat. NH4CI aq. and the products were extracted with diethyl ether. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on amino functionalized silica gel with EtOAc-n-Hexane (1 :15) to give the title compound (40 mg, 44%). 1H NMR (CDCI3): 7.01-6.88 (m, 6H), 3.67 (s, 3H), 2.89 (dt, 2H), 2.57 (dt, 2H), 2.37 (s, 3H), 2.24 (s, 3H), 2.04 (q, 4H), 1.69 (q, 4H), 1.10 (t, 6H), 0.58 (t. 6H).

(5) Preparation of 3-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenyl)-propionic acid

OH "OH

To a solution of 3-(4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenyl)-propionic acid methyl ester (compound prepared in Example 104-(4)) (40 mg, 0.089 mmol) in MeOH- H2O (10:1 , 1.1 ml) was added KOH as 0.5 tablets and the mixture was stirred at room temperature for 3 h. The reaction mixture was poured into sat. NH4CI aq. and the products were extracted with diethyl ether. The extracts were washed with water and brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on amino functionalized silica gel with CH2CI2ZMeOH (20:1) to give the title compound (19 mg, 49%). 1H NMR (CDCI3): 7.37 (d, 1H), 6.98 (m, 2H), 6.90 (m, 3H), 2.89 (dt, 2H), 2.60 (dt, 2H), 2.36 (s, 3H), 2.22 (s, 3H), 2.04 (q, 4H), 1.75 (m, 4H), 1.10 (t, 6H), 0.58 (t, 6H); MS (ESI-) : 433 ([M-HV).

Example 105 Preparation of 3-(4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenyl)-propionic acid

o (1 ) Preparation of 3-(4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenyl)-propionic acid methyl ester

H3CO. H3CO. OTf

To a solution of 3-{4-[1 -ethyl-1 -(3-methyl-4-trifluoromethanesulfonyloxy- phenyl)-propyl]-2-methyl-phenyl}-propionic acid methyl ester (compound prepared in Example 104-(3)) (170mg, 0.35mmol) in anhydrous DMF (4 ml) under nitrogen atmosphere were added triethylamine (0.058 ml, 0.42 mmol), 3-ethyl-pent-1-en-3-ol (1.0 g, 8.75 mmol), 1 ,3- bis(diphenylphosphine)propane (36 mg, 0.08 mmol) and palladium acetate (15.6 mg, 0.07 mmol). After stirring overnight at 100 degrees C, the reaction mixture was poured into water and the products were extracted with diethyl ether. The extracts were washed with water and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on amino functionalized silica gel with EtOAc-n- Hexane (1 :10) to give the title compound (10 mg, 5%). 1H NMR (CDCI3); 6.95 (m, 6H), 6.74 (d, 1 H), 6.00 (d, 1 H), 3.67 (s, 3H), 2.89 (dt, 2H), 2.57 (dt, 2H), 2.30 (s, 3H), 2.25 (s, 3H), 2.04 (q, 4H), 1.649 (q, 4H), 0.91 (t, 6H), 0.60 (t, 6H). (2) Preparation of 3-(4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenyl)-propionic acid

H3CO.

To a solution of 3-(4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenyl)-propionic acid methyl ester (compound prepared in Example 105-(1)) (10 mg, 0.022 mmol) in MeOH- H2O (10:1 , 1.1 ml) was added KOH as 0.5 tablets and the mixture was stirred at room temperature for 3 h. The reaction mixture was poured into sat. NH4CI aq. and the products were extracted with diethyl ether. The extracts were washed with water and brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on amino functionalized silica gel with CH2CI2/MeOH (20:1) to give the title compound (7.6 mg, 79%). 1H NMR (CDCI3): 6.95 (m, 6H), 6.74 (d, 1 H), 6.00 (d, 1 H), 2.90 (t, 2H), 2.62 (t, 2H), 2.30 (s, 3H), 2.25 (s, 3H), 2.04 (q, 4H), 1.63 (q, 4H), 0.91 (t, 6H), 0.60 (t, 6H); MS (ESI-) : 435([M-Hr).

Example 106 Preparation of 3-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenyl) -propionic acid

(1) Preparation of Trifluoro-methanesulfonic acid 4-{1-ethyl-1-[3-methyl-4- (4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-yn yl)-phenyl]- propyl}-2-methyl-phenyl ester

TfO I pMOM 01-3 To a solution of 4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-methoxymethoxy- 3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-pheno l (compound prepared in Example 2-(2)) (400 mg, 0.8 mmol) in dichloromethane (4 ml), Tf2O (0.15 ml, 0.89 mmol) and pyridine (0.13 ml, 1.6 mmol) were added at 0 degrees C and the mixture was stirred at 0 degrees C for 2 h. The reaction mixture was poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :20) to give the title compound (410 mg, 81 %) 1H-NMR (CDCI3): 0.60 (t, 6H, J= 7.3 Hz), 2.07 (q, 4H, J= 7.3 Hz), 2.32 (s, 3H)1 2.41 (s, 3H), 3.48 (s, 3H), 5.15 (s, 2H), 6.90-7.05 (m, 4H), 7.11 (d, 1 H, J= 9.2 Hz), 7.40 (d, 1H, J= 8.1 Hz).

(2) Preparation of (E)-3-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenyiy-acrylic acid methyl ester

TfO' XF3 CF3 ^JpMOM ^MOM "3 UC3 To a solution of Trifluoro-methanesulfonic acid 4-{1-ethyl-1-[3-methyl-4- (4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-yn yl)-phenyl]- propyl}-2-methyl-phenyl ester (compound prepared in Example 106-(1 )) (136 mg, 0.214 mmol) in DMF (2 ml) were added Pd(OAc)2 (IO mg, 0.0429 mmol), dppp (22 mg, 0.0535 mmol), Et3N (0.036 ml, 0.214 mmol) and ethylacrylae (0.029 ml, 0.321 mmol) and the mixture was stirred at 110 degrees C for 5 h. The reaction mixture was cooled to room temperature, poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :15) to give the title compound (53 mg, 43%) 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 2.07 (q, 4H), 2.37 (s, 3H), 2.38 (s, 3H), 3.46 (s, 3H), 3.79 (s, 3H)1 5.13 (s, 2H), 6.31 (d, 1 H), 6.94-7.03 (m, 4H), 7.36-7.44 (m, 2H), 7.92 (d, 1 H).

(3) Preparation of 3-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenyl)-propionic acid methyl ester

CF3 gp pMι\ OM

To a solution of (E)-3-(4-{1-ethyl-1-[3-methyl-4-(4 ,4 ,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1 -ynyl)-phenyl]-propyl}-2-methyl- phenyl)-acrylic acid methyl ester (compound prepared in Example 106-(2)) (36 mg, 0.0631 mmol) in CH2CI2 (2 ml) and MeOH (4 ml) at 0 degrees C were added NiCI2-6H2O (30 mg, 0.126 mmol), and NaBH4 (51 mg, 1.33 mmol) and the mixture was stirred at room temperature for 30 min. The reaction mixture was poured into sat. NH4CI aq. and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :25) to give the title compound (30 mg, 84%). 1H-NMR (300MHz, CDCI3): 0.52 (t, 6H), 1.99 (q, 4H), 2.17 (s, 3H), 2.32 (s, 3H), 2.50 (t, 2H), 2.82 (t, 2H), 3.40 (s, 3H), 3.60 (s, 3H), 5.13 (s, 2H), 6.79- 6.98 (m, 5H), 7.29 (d, 1H); MS (ESI+) : 573 ([M+H∏.

(4) Preparation of 3-(4-{1-ethyl-1-[3-methyl-4-(4 ,4 ,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1 -ynyl)-phenyl]-propyl}-2-methyl-phenyl)-propionic acid methyl ester

CF, ^MOM To a solution of 3-(4-{1-ethy|-1-[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluorornethyl-but-1-ynyl)-phenyl]-propyl }-2-methyl- phenyl)-propionic acid methyl ester (compound prepared in Example 106- (3)) (35 mg, 0.0611 mmol) in i-PrOH (0.8 ml) were added CBr4 (2 mg, 0.0061 mmol) and the mixture was refluxed overnight. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1:8) to give the title compound (28 mg, 86%). 1H-NMR (300MHz, CDCI3): 0.58 (t, 6H), 2.05 (q, 4H), 2.24 (s, 3H), 2.38 (s, 3H), 2.52 (t, 2H), 2.89 (m, 2H), 3.67 (s, 3H), 6.85-7.05 (m, 5H), 7.34 (d, 1 H).

(5) Preparation of 3-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenyl) -propionic acid

To a solution of 3-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenyl) -propionic acid methyl ester (compound prepared in Example 106-(4)) (30 mg, 0.0539 mmol) in MeOH (1 ml) was added 1 N- KOH(0.2 ml, 0.2 mmol) and the mixture was stirred at room temperature overnight. The reaction mixture was poured into sat. NH4CI aq. and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with CH2CI2-MeOH (20:1 ) to give the title compound (22 mg, 75%). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 2.05 (q, 4H), 2.24 (s, 3H), 2.38 (s, 3H), 2.61 (t, 2H), 2.90 (t, 2H), 3.67 (s, 3H), 6.87-7.05 (m, 5H), 7.34 (d, 1 H); MS (ESI-) : 513 ([M-H]-).

Example 107 Preparation of 3-(4-{1 -ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-i-enyO-phenylJ-propylJ^-methyl-phenylJ-p ropionic acid

o (1 ) Preparation of trifluoro-methanesulfonic acid 4-{1-ethyl-1-[3-methyl-4- ((E)-4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but- 1-enyl)-phenyl]- propyl}-2-methyl-phenyl ester

CF3 TfO __£>M0M __0M0M OF3 CF3 To a stirred solution of 4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenol (compound prepared in Example 30-(1 )) (394 mg, 0.78 mmol) in 7.80 ml of CH2CI2 were added Tf2O (0.197 ml, 1.17 mmol) and Et3N at -30 degrees C under N2 atmosphere. After stirred for 1 h, the reaction mixture was quenched with 30 ml of sat. NaHCO3 aq. and the products were extracted with CH2CI2. The extracts were washed with brine, dried over anhydrous Na2SO4, filtered and evaporated under reduced pressure. The obtained residue was purified by silica gel chromatography (n- Hexane:EtOAc=5:1) to give the title compound (440 mg, 88.7%) as colorless oil. 1H-NMR (300MHz, CDCI3): 7.40-7.30 (m, 2H), 7.15-6.95 (m, 5H), 6.10 (d, 1 H), 5.00 (s, 2H), 3.50 (s, 3H), 2.35 (s, 6H), 2.10 (q, 4H), 0.60 (t, 6H).

(2) Preparation of (E)-3-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4 ,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenyl)-acrylic acid ethyl ester

EtO CF3 TfO MOM OMOM CF3 To a stirred solution of trifluoro-methanesulfonic acid 4-{1 -ethyl- 1 -[3-methyl- 4-((E)-4,4)4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-bu t-1-enyl)- phenyl]-propyl}-2-methyl-phenyl ester (compound prepared in Example 107- (1 )) (234 mg, 0.37 mmol) in DMF (3.7 ml) were added Pd(OAc)2 (16.6 mg, 5 20 mol%), dppp (38.2 mg, 25 mol%), ethylacrylate (0.40 ml, 3.70 mmol) and Et3N (0.103 ml, 0.74 mmol) at room temperature under N2 atmosphere. Then the reaction mixture was stirred at 110 degrees C for 16 h. The reaction mixture was cooled to room temperature, poured into water and the products were extracted with EtOAc. The extracts were dried over anhydrous 0 Na2SO4, filtered and evaporated under reduced pressure. The obtained residue was purified by silica gel chromatography (n-Hexane:EtOAc=10:1) to give the title compound (138 mg, 63.6%) as colorless sticky oil. 1H-NMR(300MHz, CDCI3): 7.95 (d, 1 H), 7.50-7.35 (m, 3H), 7.05-6.95 (m, 4H), 6.35 (d, 1 H), 6.08 (d, 1H), 5.00 (s, 2H), 4.25 (q, 2H), 3.50 (s, 3H), 2.40 5 (S, 3H), 2.35 (s, 3H), 2.10 (q, 4H), 1.35 (t, 3H), 0.60 (t, 6H).

(3) Preparation of 3-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenyl)-propionic acid ethyl ester

Q O ' ' CFg --- O ' I CF?MOM To a stirred solution of (E)-3-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenyl)-acrylic acid ethyl ester (compound prepared in Example 107-(2)) (138 mg, 0.24 mmol) in MeOH/CH2CI2 (2/1 v/v, 30 ml) was added NiCI2 5 6H2O(114 mg, 0.48 mmol) and NaBH4 at 0 degrees C under N2 atmosphere and the mixture was stirred for 1 h. The reaction mixture was poured into sat. NH4CI aq. and the products were extracted with EtOAc. The extracts were dried over anhydrous Na2SO4, filtered and evaporated under reduced pressure. The obtained residue was purified by silica gel chromatography (n-Hexane:EtOAc=10:1) to give the title compound (116 mg, 82.3%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.40-7.30 (m, 2H), 7.05-6.85 (m, 5H), 6.08 (d, 1 H), 5.00 (s, 2H), 4.15 (q, 2H), 3.50 (s, 3H), 2.90 (t, 2H), 2.55 (t, 2H), 2.35 (s, 3H), 2.30 (s, 3H), 2.10 (q, 4H), 1.35 (t, 3H), 0.60 (t, 6H).

(4) Preparation of Preparation of 3-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-pr opyl}-2-methyl- phenyl)-propionic acid

,.CF3 »- ό ■ i CF?M0M To a stirred solution of 3-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenyl)-propionic acid ethyl ester (compound prepared in Example 107-(3)) (116 mg, 0.20 mmol) in EtOH (2 ml) was added CBr4 (6.60 mg, 10 mol%) under N2 atmosphere at room temperature. The reaction mixture was refluxed for 4.5 h. The reaction mixture was poured into water and the products were extracted with EtOAc. The extracts were washed with water and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :10) to give 3-(4-{1-ethyl-1-[3-methyl-4-((E)-4,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phe nyl]-propyl}-2- methyl-phenyl)-propionic acid ethyl ester (84.0 mg, 78.5%) as colorless sticky oil. To a stirred solution of 3-(4-{1 -ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenyl)-propionic acid ethyl ester (84.0 mg, 0.15 mmol) in EtOH/Water (4/1 v/v, 1.9 ml) was added KOH (16.8 mg, 0.30 mmol) at room temperature and the reaction mixture was stirred for 4 h. The reaction mixture was poured into 0.1 N-HCI and the products were extracted with EtOAc. The extracts were washed with water and brine, dried over anhydrous Na2SO4, filtered and evaporated under reduced pressure. The obtained residue was purified by silica gel chromatography (n-Hexane: EtOAc=I :1 ) to give the title compound (69.0 mg, 89.0%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.40-7.30 (m, 2H)1 7.05-6.85 (m, 5H), 6.10 (d, 1 H), 2.90 (t, 2H), 2.65 (t, 2H), 2.35 (s, 3H), 2.25 (s, 3H), 2.15-2.00 (m, 5H), 0.60 (t, 6H); MS (ESI-) : 515 ([M-H]").

Example 108 Preparation of 3-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenyl)-propionic acid

OH (1 ) Preparation of trifluoro-methanesulfonic acid 4-{1-[4-(4,4-dimethyl-3-oxo- pentyl)-3-methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl ester

TfO ό ' ' o To a solution of 1-{4-[1-ethyl-1-(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenyl}-4,4-dimethyl-pentan-3-one (compound prepared in Example 18-(3)) (410 mg, 1.07 mmol) in anhydrous CH2Cb (10 ml) under nitrogen atmosphere were added trifluoromethanesulfonic anhydride (0.26 ml, 1.6 mmol) and pyridine (0.26 ml, 3.21 mmol) and the mixture was stirred at room temperature for 1 h. The reaction mixture was poured into sat. NH4CI aq. and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :7) to give the title compound (470 mg, 85%). 1H NMR (CDCI3): 7.10-6.97 (m, 4H), 6.88 (m, 2H), 2.82 (m, 2H), 2.72 (m, 2H), 2.31 (s, 3H), 2.25 (s, 3H), 2.04 (q, 4H), 1.10 (s, 9H), 0.59 (t, 6H). (2) Preparation of (E)-3-(4-{1-[4-(4,4-dimethyl-3-oxo-pentyl)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-acrylic acid methyl ester

H3CO. TfO' O O 1 1 O To a solution of trifluoro-methanesulfonic acid 4-{1-[4-(4,4-dimethyl-3-oxo- pentyl)-3-methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl ester (compound prepared in Example 108-(1 )) (470 mg, 0.91 mmol) in anhydrous DMF (10 ml) under nitrogen atmosphere were added triethylamine (0.15 ml, 1.08 mmol), methylacrylate (0.12 ml, 1.3 mmol), 1 ,3- bis(diphenylphosphine)propane (93 mg, 0.22 mmol) and palladium acetate (40 mg, 0.18 mmol). The reaction mixture was stirred at 100 degrees C for 1.5 h and poured into sat. NH4CI aq. and the products were extracted with ethyl acetate. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :7) to give the title compound (230 mg, 56%). 1H NMR (CDCI3): 7.95 (d, 1 H), 7.42 (d, 1 H), 7.04-6.96 (m, 3H), 6.90 (m, 2H), 6.32 (d, 1 H), 3.79 (s, 3H), 2.82 (m, 2H), 2.71 (m, 2H), 2.38 (s, 3H), 2.24 (s, 3H), 2.06 (q, 4H), 1.09 (s, 9H), 0.60 (t, 6H).

(3) Preparation of (E)-3-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenyl)-acrylic acid methyl ester

H3CO. H3CO. O O To a solution of (E)-3-(4-{1-[4-(4,4-dimethyl-3-oxo-pentyl)-3-methyl-phenyl]- 1-ethyl-propyl}-2-methyl-phenyl)-acrylic acid methyl ester (compound prepared in Example 108-(2)) (220 mg, 0.49 mmol) in methanol (5 ml) under nitrogen atmosphere was added sodium borohydride (37 mg, 0.98 mmol) and the mixture was stirred at room temperature for 1.5 h. The reaction mixture was poured into water and the products were extracted with ethyl acetate. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :7) to give the title compound (160 mg, 72%). 1H NMR (CDCI3): 7.95 (d, 1 H), 7.43 (d, 1 H), 7.04-6.98 (m, 3H), 6.91 (m, 2H), 6.31 (d, 1 H), 3.79 (s, 3H), 3.24 (m, 1 H)1 2.86 (m, 1 H), 2.56 (m, 1 H), 2.39 (s, 3H), 2.25 (s, 3H), 2.08 (q, 4H), 1.79 (m, 1 H), 1.48 (m, 1 H), 0.89 (s, 9H), 0.61 (t, 6H).

(4) Preparation of 3-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenyl)-propionic acid

OH To a solution of (E)-3-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenyl)-acrylic acid methyl ester (compound prepared in Example 108-(3)) (160 mg, 0.35 mmol) in methanol (3 ml) was added 10% palladium carbon (10 mg) and the mixture was stirred overnight at room temperature under hydrogen atmosphere. The reaction mixture was filtered through celite and the filtrate was concentrated under reduced pressure. The obtained residue was dissolved in methanol (3 ml)/H2θ (0.1 ml). To the mixture was added KOH as 1 tablet and the mixture was stirred at room temperature for 30 min. The reaction mixture was poured into 0.1 N- HCI and the products were extracted with ethyl acetate. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :3) to give the title compound (110 mg, 71 % for two steps) as a solid. 1H NMR (CDCI3): 7.03-6.89 (m, 6H)1 3.25 (dt, 1 H), 2.86 (m, 3H), 2.58 (m, 3H), 2.25 (s, 6H), 2.04 (q, 4H), 1.79 (m, 1 H), 1.50 (m, 1 H), 0.88 (s, 9H), 0.59 (t, 6H); MS (ESI-) : 437 ([M-HV). Example 109 Preparation of (E)-3-ethyl-1-[4-(1-ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)- butoxy]-phenyl}-propyl)-2-methyl-phenyl]-pent-1-en-3-ol

N-NH

(1) Preparation of 5-(4-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanenitrile

To a stirred solution of 4-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1- (5)) (274 mg, 0.72 mmol) and 5-Bromovaleronitrile (350 mg, 2.16 mmol) in 7.20ml of anhydrous DMF was added K2CO3 (299 mg, 2.16 mmol) under N2 atmosphere at room temperature. The reaction mixture was stirred at 100 degrees C for 12 h. The reaction mixture was cooled to room temperature, poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :6) to give the title compound (184 mg, 55%) as colorless oil. 1H-NMR (300MHz, CDCI3): 7.30 (d, 1 H), 7.00-6.85 (m, 4H), 6.75 (d, 1 H), 6.65 (d, 1 H), 6.00 (d, 1H), 4.00 (t, 2H), 2.50 (t, 2H), 2.35 (s, 3H), 2.25 (s, 3H), 2.15 (s, 3H), 2.10-1.85 (m, 8H), 1.70-1.55 (m, 4H), 0.90 (t, 6H), 0.60 (t, 6H).

(2) Preparation of (E)-3-ethyl-1-[4-(1-ethyl-1-{3-methyl-4-[4-(1H-tetrazol-5- yl)-butoxy]-phenyl}-propyl)-2-methyl-phenyl]-pent-1-en-3-ol To a solution of 5-(4-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanenitrile (compound prepared in Example 109-(1)) (46.5 mg, 0.10 mmol) in anhydrous toluene (1.2 ml) was added Me3SnN3 (61.7 mg, 0.30 mmol) and the mixture was stirred at 110 degrees C for 12 h. The reaction mixture was cooled to room temperature, poured into water and the products were extracted with EtOAc. The extracts were washed with water and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with ChbCfe: MeOH (50:1) to give the title compound (13 mg, 26%) as amorphous. 1H-NMR(300MHz, CDCI3): 7.30 (d, 1H), 7.00-6.85 (m, 4H), 6.75 (d, 1H), 6.65 (d, 1H), 6.00 (d, 1H), 3.98 (t, 2H), 3.10 (t, 2H), 2.35 (s, 3H), 2.25 (s, 3H), 2.15 (s, 3H), 2.10-1.95 (m, 8H), 1.90-1.80 (m, 2H), 1.70-1.55 (m, 4H), 0.90 (t, 6H), 0.60 (t, 6H); MS (ESI-) : 503 ([M-H]+).

Example 110 Preparation of 1-[4-(1 -ethyl- 1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]- phenyl}-propyl)-2-methyl-phenylethynyl]- cyclopentanol

N-NH

(1 preparation of 5-(4-{1 -ethyl-1 -[4-(1-hydroxy-cyclopentylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-pentanenitrile

NC OH Using the same procedure as described for the preparation of Example 109-(1), the title compound was prepared from 4-{1-Ethyl-1-[4-(1-hydroxy- cyclopentylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 7). The yield was 55%. 1H-NMR (300MHz, CDCI3): 7.30 (d, 1 H), 7.00 (bs, 1 H), 6.95-6.85 (m, 2H), 6.85 (bs, 1 H), 6.65 (d, 1 H), 3.98 (t, 2H), 2.50 (t, 2H), 2.38 (s, 3H), 2.15 (s, 3H), 2.10-1.70 (m, 17H), 0.60 (t, 6H).

(2) Preparation of 1-[4-(1-ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]- phenyl}-propyl)-2-methyl-phenylethynyl]- cyclopentanol

Using the same procedure as described for the preparation of Example 109-(2), the title compound was prepared from 5-(4-{1-Ethyl-1-[4-(1-hydroxy- cyclopentylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenox y)- pentanenitrile (compound prepared in Example 110-(1 )). The yield was 44%. 1H-NMR (300MHz, CDCI3): 7.25 (d, 1 H), 7.00 (bs, 1 H), 6.95-6.85 (m, 2H), 6.85 (bs, 1 H), 6.65 (d, 1 H), 3.98 (t, 2H), 3.15 (t, 2H), 2.35 (s, 3H), 2.15 (s, 3H), 2.10-1.70 (m, 17H), 0.60 (t, 6H); MS (ESI-) : 499 ([M-H]").

Example 111 Preparation of 1-{(E)-2-[4-(1-ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]- phenyl}-propyl)-2-methyl-phenyl]-vinyl}-cyclopentanol

(1) Preparation of 5-[4-(1-ethyl-1-{4-[(E)-2-(1-hydroxy-cyclopentyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanenitrile Using the same procedure as described for the preparation of Example 109-(1 ), the title compound was prepared from 4-(1-Ethyl-1-{4-[(E)-2-(1- hydroxy-cyclopentyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methy l-phenol (compound prepared in Example 10). The yield was 96%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.69-1.97 (m, 8H), 2.00-2.07 (m, 6H), 2.14 (s, 3H), 2.30 (s, 3H), 2.46 (t, 2H), 3.97 (t, 2H), 6.25 (d, 1 H), 6.66 (d, 1 H), 6.83 (d, 1 H), 6.90-6.95 (m, 4H), 7.32 (d, 1 H).

(2) Preparation of 1-{(E)-2-[4-(1-ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)- butoxy]-phenyl}-propyl)-2-methyl-phenyl]-vinyl}-cyclopentano l

Using the same procedure as described for the preparation of Example 109-(2), the title compound was prepared from 5-[4-(1-ethyl-1-{4-[(E)-2-(1- hydroxy-cyclopentyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methy l-phenoxy]- pentanenitrile (compound prepared in Example 111-(1 )). The yield was 4%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.69-1.95 (m, 8H), 2.00-2.09 (m, 6H), 2.15 (s, 3H), 2.30 (s, 3H), 3.10 (t, 2H), 4.00 (t, 2H), 6.25 (d, 1 H), 6.68 (d, 1 H), 6.83 (d, 1H), 6.90-6.95 (m, 4H), 7.32 (d, 1H); MS (ESI-) : 501 ([M-H]-

Example 112 Preparation of 1 -[4-(1 -ethyl-1 -{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]-phenyl}-propyl)-2- methyl-phenylethynyl]-cyclohexanol N-NH

(1) Preparation of 5-(4-{1-Ethyl-1-[4-(1-hydroxy-cyclohexylethynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-pentanenitrile

Using the same procedure as described for the preparation of Example 109-(1 ), the title compound was prepared from 4-{1-ethyl-1-[4-(1-hydroxy- cyclohexylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 8). The yield was 70%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.57-2.00 (m, 14H), 2.03 (q, 4H), 2.14 (S, 3H), 2.38 (s, 3H), 2.50 (t, 2H), 3.98 (t, 2H), 6.66 (d, 1H), 6.85-7.00 (m, 4H), 7.27 (d, 1 H).

(2) Preparation of 1-[4-(1-ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]- phenyl}-propyl)-2-methyl-phenylethynyl]-cyclohexanol

Using the same procedure as described for the preparation of Example 109-(2), the title compound was prepared from 5-(4-{1-Ethyl-1-[4-(1-hyd roxy- cyclohexylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy )- pentanenitrile (compound prepared in Example 112-(1 )). The yield was 26%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.57-2.00 (m, 14H), 2.03 (q, 4H), 2.14 (s, 3H), 2.37 (s, 3H), 3.10 (t, 2H), 3.99 (t, 2H), 6.67 (d, 1 H), 6.86-7.00 (m, 4H), 7.26 (d, 1 H); MS (ESI+) : 537 ([M+Na]+). Example 113 Preparation of 1-{(E)-2-[4-(1-Ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)- butoxy]-phenyl}-propyl)-2-methyl-phenyl]-vinyl}-cyclohexanol

N-NH

(1 ) Preparation of 5-[4-(1-ethyl-1-{4-[(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentanenitrile

Using the same procedure as described for the preparation of Example 109-(1), the title compound was prepared from 4-(1-ethyl-1-{4-[(E)-2-(1- hydroxy-cyclohexyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methyl -phenol (compound prepared in Example 11). The yield was 73%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.57-2.00 (m, 14H), 2.04 (q, 4H), 2.14 (S1 3H), 2.30 (s, 3H), 2.44 (m, 2H), 3.98 (t, 2H), 6.20 (d, 1H), 6.66 (d, 1H), 6.81 (d, 1 H), 6.90-6.96 (m, 4H), 7.32 (d, 1H).

(2) Preparation of 1-{(E)-2-[4-(1-ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)- butoxy]-phenyl}-propyl)-2-methyl-phenyl]-vinyl}-cyclohexanol

Using the same procedure as described for the preparation of Example 109-(2), the title compound was prepared from 5-[4-(1-Ethyl-1-{4-[(E)-2-(1- hydroxy-cyclohexyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methyl -phenoxy]- pentanenitriie (compound prepared in Example 113-(1)). The yield was 24%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.57-2.00 (m, 14H), 2.04 (q, 4H), 2.14 (s, 3H), 2.29 (s, 3H), 3.10 (t, 2H), 3.98 (t, 2H), 6.20 (d, 1 H), 6.67 (d, 1 H), 6.81 (d, 1 H), 6.90-6.96 (m, 4H), 7.31 (d, 1 H); MS (ESI-) : 515 ([M-H]").

Example 114 Preparation of 4-[4-(1-ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]- phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-yn-2- ol

(1 ) Preparation of 5-[4-(4-{1 -ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenoxy)-butyl]-1 H-tetrazole

.CF3 <TF?M0M CF°MOM ' ' a? M' OM Using the same procedure as described for the preparation of Example 109- (1 ), 5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-methoxymethoxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentanenitrile was prepared from 4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenol (compound prepared in Example 2-(2)). The yield was 99%. Using the same procedure as described for the preparation of Example 109- (2), the title compound was prepared from 5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenoxy)-pentanenitrile. The yield was 66%. 1H-NMR (300MHz, CDCI3): 7.40 (d, 1H), 7.05 (bs, 1H), 7.00-6.85 (m, 2H), 6.82 (bs, 1 H), 6.65 (d, 1 H), 5.15 (s, 2H), 4.00 (t, 2H), 3.50 (s, 3H), 3.15 (t, 2H), 2.40 (s, 3H), 2.15 (s, 3H), 2.15-2.00 (m, 6H), 2.00-1.80 (m, 2H), 0.60 (t, 6H). (2) Preparation of 4-[4-(1-ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]- phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-yn-2- ol

N-N

^OMOM GF3 To a solution of 5-[4-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenoxy)-butyl]-1 H-tetrazole (compound prepared in Example 114-(1)) (21.0 mg, 0.03 mmol) in MeOH (0.34 ml) was added pTsOH (9.70 mg, 0.05 mmol) and the mixture was stirred at 60 degrees C for 12 h. The reaction mixture was concentrated under reduced pressure and the obtained residue was purified by silica gel chromatography (CH2Cl2:MeOH=30:1) to give the title compound (16.0 mg, 80.8%) as colorless sticky oil 1H-NMR (300MHz, CDCI3): 7.30 (d, 1 H), 7.05 (bs, 1H), 7.00-6.80 (m, 3H), 6.65 (d, 1 H), 3.98 (t, 2H), 3.10 (t, 2H), 2.35 (s, 3H), 2.15 (s, 3H), 2.15-2.00 (m, 6H), 2.00-1.80 (m, 2H), 0.60 (t, 6H); MS (ESI-) : 581 ([M-H∏.

Example 115 Preparation of (E)-4-[4-(1-Ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]- phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2- ol

(1) Preparation of 5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxy)-pentanenitrile ^-IOMOM CF3 ^JDMOM CF3 Using the same procedure as described for the preparation of Example 109-(1 ), the title compound was prepared from 4-{1-Ethyl-1-[3-methyl-4-((E)- 4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-eny l)-phenyl]- propyl}-2-methyl-phenol (compound prepared in Example 30-(1 )). The yield was 90%. 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 1.83-2.04 (m, 4H), 2.05 (q, 4H), 2.15 (s, 3H), 2.31 (s, 3H), 2.41 (t, 2H), 3.50 (s, 3H), 3.98 (t, 2H), 4.97 (s, 2H), 6.06 (d, 1 H), 6.66 (d, 1 H), 6.89-7.02 (m, 4H), 7.30-7.39 (m, 2H).

(2) Preparation of 5-[4-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxy)-butyl]-1 H-tetrazole

,N-NH

,.,JOMOM ^JOMOM CF3 CF3 Using the same procedure as described for the preparation of Example 109-(2), the title compound was prepared from 5-(4-{1-ethyl-1-[3-methyl-4- ((E)-4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but- 1-enyl)-phenyl]- propyl}-2-methyl-phenoxy)-pentanenitrile (compound prepared in Example 115-(1 )). The yield was 60%. 1H-NMR (300MHz, CDCI3): 0.61 (t, 6H), 1.83-2.04 (m, 4H), 2.05 (q, 4H), 2.15 (s, 3H), 2.32 (s, 3H), 3.11 (m, 2H), 3.50 (s, 3H), 4.00 (t, 2H), 4.96 (s, 2H), 6.06 (d, 1 H), 6.69 (d, 1H), 6.89-7.02 (m, 4H), 7.30-7.39 (m, 2H).

(3) Preparation of (E)-4-[4-(1-ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)- butoxy]-phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but- 3-en-2-ol ,N-NH

Using the same procedure as described for the preparation of Example 114-(2), the title compound was prepared from 5-[4-(4-{1-ethyl-1-[3-methyl-4- ((E)-4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but- 1-enyl)-phenyl]- propyl}-2-methyl-phenoxy)-butyl]-1 H-tetrazole (compound prepared in Example 115-(2)). The yield was 61 %. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.83-2.04 (m, 4H)1 2.05 (q, 4H), 2.14 (s, 3H), 2.32 (s, 3H), 3.12 (t, 2H), 4.00 (t, 2H), 6.08 (d, 1H)1 6.68 (d, 1H), 6.89-7.00 (m, 4H), 7.30-7.39 (m, 2H); MS (ESI-) : 583 ([M-H]").

Example 116 Preparation of 1-[4-(1 -ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]- phenyl}-propyl)-2-methyl-phenyl]-4,4-dimethyl-pentan-3-ol

(1 ) Preparation of 5-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanenitrile

Using the same procedure as described for the preparation of Example 109-(1), the title compound was prepared from 4-{1-ethyl-1~[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno l (compound prepared in Example 18). The yield was 98%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.38 (m, 1 H), 1.43-1.53 (m, 1H), 1.74-1.97 (m, 5H), 2.04 (q, 4H), 2.15 (s, 3H), 2.25 (s, 3H), 2.46 (d, 2H), 2.52-2.60 (m, 1 H), 2.81-2.91 (m, 1 H), 3.24 (d, 1 H), 3.97 (t, 2H), 6.65 (d, 1 H), 6.90-6.96 (m, 4H), 7.01 (d, 1 H). (2) Preparation of 1-[4-(1-ethyl-1-{3-methyl-4-[4-(1 H-tetrazol-5-yl)-butoxy]- phenyl}-propyl)-2-methyl-phenyl]-4,4-dimethyl-pentan-3-ol

Using the same procedure as described for the preparation of Example 109-(2), the title compound was prepared from 5-(4-{1-ethyl-1-[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)- pentanenitrile (compound prepared in Example 116-(1 )). The yield was 65%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H)1 0.89 (s, 9H), 1.38 (m, 1 H), 1.44-1.58 (m, 1H), 1.76-1.91 (m, 3H), 1.99-2.08 (m, 6H), 2.13 (s, 3H), 2.25 (s, 3H), 2.52-2.62 (m, 1 H), 2.80-2.89 (m, 1 H), 3.08 (t, 2H), 3.26 (dd, 1 H), 3.98 (t, 2H), 6.65 (d, 1 H), 6.89-6.95 (m, 4H), 7.01 (d, 1 H); MS (ESI-) : 505 ([M-HV).

Example 117 Preparation of 1-[4-(1 -ethyl- 1-{3-methyl-4-[5-(1 H-tetrazol-5-yl)-pentyloxy]- phenyl}-propyl)-2-methyl-phenyl]-4,4-dimethyl-pentan-3-ol

5N-NH (1 ) Preparation of 6-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-hexanenitrile

Using the same procedure as described for the preparation of Example 109-(1 ), the title compound was prepared from 4-{1-ethyl-1-[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno l (compound prepared in Example 18) and 6-bromohexanenitrile. The yield was 89%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.41-1.87(m, 8H), 2.04 (q, 4H), 2.15 (s, 3H), 2.25 (s, 3H), 2.38 (t, 2H), 2.50-2.60 (m, 1 H), 2.81-2.91 (m, 1 H), 3.24 (dd, 1 H), 3.94 (t, 2H), 6.65 (d, 1 H), 6.89-6.95 (m, 4H), 7.01 (d, 1 H).

(2) Preparation of 1-[4-(1-Ethyl-1-{3-methyl-4-[5-(1 H-tetrazol-5-yl)-pentyloxy]- phenyl}-propyl)-2-methyl-phenyl]-4,4-dimethyl-pentan-3-ol

Using the same procedure as described for the preparation of Example 109-(2), the title compound was prepared from 6-(4-{1-Ethyl-1-[4-(3-hyd roxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)- hexanenitrile (compound prepared in Example 117-(1)). The yield was 52%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.44-1.62 (m, 3H), 1.76-1.94 (m, 5H), 2.03 (q, 4H), 2.11 (s, 3H), 2.24 (s, 3H), 2.52-2.62 (m, 1 H), 2.79-2.89 (m, 1H), 2.99 (t, 2H), 3.26 (dd, 1H), 3.92 (t, 2H), 6.63 (d, 1 H), 6.90- 6.93 (m, 4H), 7.01 (d, 1 H); MS (ESI-) : 519 ([M-H]").

Example 118 Preparation of 1 -(4-{1 -[4-(5-amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl- propyl}-2-methyl-phenyl)-3-ethyl-pent-1-yn-3-ol H9N

(1) Preparation of 2-[5-(4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3-meth yl- phenyl]-propyl}-2-methyl-phenoxy)-pentyl]-isoindole-1 ,3-dione

Using the same procedure as described for the preparation of Example 102-(1), the title compound was prepared from 4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1- ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(4)). The yield was 57%. 1H NMR (CDCI3): 7.84 (m, 2H), 7.70 (m, 2H), 7.26 (m, 1 H), 7.00 (m, 1 H), 6.91 (m, 2H), 6.82 (m, 1 H), 6.64 (d, 1H), 3.91 (t, 2H), 3.70 (t, 2H), 2.36 (s, 3H), 2.09 (s, 3H), 2.04 (q, 4H), 1.91 (m, 4H), 1.75 (m, 4H), 1.25 (t, 2H), 1.10 (t, 6H), 0.58 (t, 6H).

(2) Preparation of 1-(4-{1-[4-(5-amino-pentyloxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-3-ethyl-pent-1-yn-3-ol

To a solution of 2-[5-(4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-ynyl)-3-meth yl- phenyl]-propyl}-2-methyl-phenoxy)-pentyl]-isoindole-1 ,3-dione (compound prepared in Example 118-(1)) (90 mg, 0.15 mmol) in EtOH (1 ml) under nitrogen atmosphere was added methylamine (0.3 ml, 40 wt% in water) and the mixture was stirred at room temperature for 2 h. The reaction mixture was concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with CH2CI2:MeOH (5:1 ) to give the title compound (14 mg, 20%). 1H NMR (CDCI3): 7.27 (m, 1 H), 7.00 (m, 1 H), 6.90 (m, 2H), 6.84 (m, 1 H), 6.65 (d, 1 H), 3.92 (t, 2H), 2.74 (m, 2H), 2.56 (br, NH2), 2.37 (s, 3H), 2.13 (s, 3H), 2.04 (q, 4H), 1.75 (m, 6H), 1.10 (t, 6H), 0.58 (t, 6H); MS (ESI+) : 464 ([M+H]+).

Example 119 Preparation of (E)-1-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-3-ethyl-pent-1-en-3-ol

(1 preparation of 2-[5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentyl]-isoindole-1 ,3-dione

Using the same procedure as described for the preparation of Example 102-(1), the title compound was prepared from 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy- pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(5)). The yield was 34%. 1H NMR (CDCI3): 7.84 (m, 2H), 7.70 (m, 2H), 6.93 (m, 5H), 6.74 (d, 1 H), 6.64 (d, 1 H), 6.00 (d, 1 H), 3.91 (t, 2H), 3.72 (t, 2H), 2.30 (s, 3H), 2.10 (s, 3H), 2.04 (q, 4H), 1.79 (m, 4H), 1.64 (q, 4H), 1.25 (t, 2H), 0.91 (t, 6H), 0.60 (t, 6H).

(2) Preparation of (E)-1-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-3-ethyl-pent-1-en-3-ol

Using the same procedure as described for the preparation of Example 118-(2), the title compound was prepared from 2-[5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-pentyl]- isoindole-1 ,3-dione (compound prepared in Example 119-(1)). The yield was 24%. 1H NMR (CDCI3): 7.29 (m, 1H), 6.91 (m, 4H), 6.74 (d, 1H), 6.63 (d, 1H), 6.00 (d, 1 H)1 3.87 (t, 2H), 3.75 (br, NH2), 2.74 (m, 2H), 2.29 (s, 3H), 2.13 (s, 3H), 2.04 (q, 4H), 1.74 (m, 2H), 1.66-1.46 (m, 8H), 0.91 (t, 6H), 0.60 (t, 6H); MS (ESI+) : 466 ([M+H]+).

Example 120 Preparation of 1 -(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl-propyl}-2- methyl-phenylethynyl)-cyclopentanol

(1 ) Preparation of 2-[5-(4-{1-Ethyl-1-[4-(1-hydroxy-cyclopentylethynyl)-3-methy l- phenyl]-propyl}-2-methyl-phenoxy)-pentyl]-isoindole-1,3-dion e

Using the same procedure as described for the preparation of Example 102-(1 ), the title compound was prepared from 4-{1-Ethyl-1-[4-(1-hydroxy- cyclopentylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 7). The yield was 68%. 1H-NMR (300MHz, CDCI3): 0.58 (t, 6H), 1.47-1.58 (m, 4H), 1.72-1.88 (m, 6H), 1.98-2.05 (q, 8H), 2.09 (s, 3H), 2.35 (s, 3H), 3.72 (t, 2H), 3.91 (t, 2H), 6.64 (d, 1H), 6.81-7.00 (m, 5H), 7.68-7.71 (m, 2H), 7.82-7.85 (m, 2H).

(2) Preparation of 1-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenylethynyl)-cyclopentanol Using the same procedure as described for the preparation of Example 100-(2), the title compound was prepared from 2-[5-(4-{1-Ethyl-1-[4-(1-hydroxy- cyclopentylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenox y)-pentyl]- isoindole-1 ,3-dione (compound prepared in Example 120-(1)). The yield was 74%. 1H-NMR (300MHz, CDCI3): 0.58 (t, 6H), 1.47-1.58 (m, 4H), 1.72-1.92 (m, 6H), 1.98-2.07 (q, 8H)1 2.14 (s, 3H), 2.36 (s, 3H), 2.72 (t, 2H), 2.92 (t, 2H), 6.66 (d, 1 H), 6.83-7.00 (m, 5H); MS (ESI+) : 462 ([M+H∏.

Example 121 Preparation of 1 -[(E)-2-(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl- propyl}-2-methyl-phenyl)-vinyl]-cyclopentanol

OH H2N^-^^O

(1) Preparation of 2-{5-[4-(1-Ethyl-1-{4-[(E)-2-(1-hydroxy-cyclopentyl)-vinyl]- 3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentyl}-isoindole-1 ,3-dione

HO OH

Using the same procedure as described for the preparation of Example 102-(1), the title compound was prepared from 4-(1-Ethyl-1-{4-[(E)-2-(1-hydroxy- cyclopentyl)-vinyl]-3-methyl-phenyl}-propyl)-2-methyl-phenol (compound prepared in Example 10). The yield was 63%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.47-1.88 (m, 14H), 2.02 (q, 4H), 2.10 (s, 3H), 2.38 (s, 3H), 3.72 (t, 2H), 3.92 (t, 2H), 6.66 (d, 1 H), 6.82-7.00 (m, 4H), 7.27 (d, 1H). (2) Preparation of 1-[(E)-2-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-eth yl- propyl}-2-methyl-phenyl)-vinyl]-cyclopentanol

Using the same procedure as described for the preparation of Example 118-(2), the title compound was prepared from 2-{5-[4-(1-Ethyl-1-{4-[(E)-2-(1-hydroxy- cyclopentyO-vinyll-S-methyl-phenylJ-propyO^-methyl-phenoxyJ- pentylJ-isoindole- 1 ,3-dione (compound prepared in Example 121-(1 )). The yield was 49%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.52 (m 4H), 1.70-1.99 (m, 10H), 2.04 (q, 4H), 2.15 (s, 3H), 2.31 (s, 3H), 2.72 (t, 2H), 3.93 (d, 2H), 6.25 (d, 1 H), 6.67 (d, 1 H), 6.68-6.96 (m, 5H), 7.31-7.34 (m, 1 H); MS (ESI+) : 464 ([M+H]+).

Example 122 Preparation of 1 -(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl-propyl}-2- methyl-phenylethynyl)-cyclohexanol

(1 ) Preparation of 2-[5-(4-{1-Ethyl-1-[4-(1-hydroxy-cyclohexylethynyl)-3-methyl - phenyl]-propyl}-2-methyl-phenoxy)-pentyl]-isoindole-1 ,3-dione

Using the same procedure as described for the preparation of Example 102-(1 ), the title compound was prepared from 4-{1-Ethyl-1-[4-(1-hydroxy- cyclohexylethynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 8). The yield was 83%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.47-1.88 (m, 16H), 2.02 (q, 4H), 2.10 (s, 3H), 2.38 (s, 3H), 3.72 (t, 2H), 3.92 (t, 2H), 6.65 (d, 1 H), 6.82-7.00 (m, 4H), 7.27 (d, 1 H), 7.71 (m, 2H), 7.84 (m, 2H).

(2) Preparation of 1-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenylethynyl)-cyclohexanol

Using the same procedure as described for the preparation of Example 118-(2), the title compound was prepared from 2-[5-(4-{1-Ethyl-1-[4-(1-hyd roxy- cyclohexylethynyO-S-methyl-phenylJ-propyl^-methyl-phenoxyJ-p entyll-isoindole- 1 ,3-dione (compound prepared in Example 122-(1)). The yield was 34%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.47-1.88 (m, 16H), 2.03 (q, 4H), 2.14 (s, 3H), 2.38 (s, 3H), 3.73 (m, 2H), 3.92 (t, 2H), 6.66 (d, 1H), 6.82-7.00 (m, 4H), 7.27 (d, 1 H); MS (ESI+) : 476 ([M+H∏.

Example 123 Preparation of 1 -[(E)-2-(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl- propyl}-2-methyl-phenyl)-vinyl]-cyclohexanol

(1) Preparation of 2-{5-[4-(1-Ethyl-1-{4-[(E)-2-(1-hydroxy-cyclohexyl)-vinyl]-3 - methyl-phenyl}-propyl)-2-methyl-phenoxy]-pentyl}-isoindole-1 ,3-dione

Using the same procedure as described for the preparation of Example 102-(1), the title compound was prepared from 4-(1 -Ethyl-1 -{4-[(E)-2-(1 -hydroxy- cyclohexyl)-vinyl]-3-methyl-pheny|}-propyl)-2-methyl-phenol (compound prepared in Example 11). The yield was 89%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.32-1.85 (m, 16H), 2.03 (q, 4H), 2.10 (s, 3H), 2.30 (s, 3H), 3.72 (t, 2H), 3.91 (t, 2H), 6.20 (d, 1 H), 6.65 (d, 1 H), 6.78- 6.95 (m, 5H), 7.31 (d, 1 H), 7.71 (m, 2H), 7.84 (m, 2H).

(2) Preparation of 1-[(E)-2-(4-{1-[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-eth yl- propyl}-2-methyl-phenyl)-vinyl]-cyclohexanol

Using the same procedure as described for the preparation of Example 118-(2), the title compound was prepared from 2-{5-[4-(1-Ethyl-1-{4-[(E)-2-(1-hydroxy- cyclohexyO-vinylJ-S-methyl-phenylJ-propyl^-methyl-phenoxyl-p entylJ-isoindole- 1 ,3-dione (compound prepared in Example 123-(1)). The yield was 34%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.32-1.85 (m, 16H), 2.04 (q, 4H), 2.15 (s, 3H), 2.30 (s, 3H), 3.73 (m, 2H), 3.93 (t, 2H), 6.20 (d, 1 H), 6.66 (d, 1 H), 6.81 (d, 1 H), 6.89-6.95 (m, 4H), 7.32 (d, 1 H); MS (ESI+) : 478 ([M+H]+).

Example 124 Preparation of 4-(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl-propyl}-2- methyl-phenyl)-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-yn-2-ol

(1 ) Preparation of 2-[5-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenoxy)-pentyl]-isoindole-1 ,3-dione ^ZOMOM __OMOM CF3 Oh3 Using the same procedure as described for the preparation of Example 102-(1 ), the title compound was prepared from 4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl-phenol (compound prepared in Example 2-(2)). The yield was 86%. 1H-NMR (300MHz, CDCI3): 7.85 (m, 2H), 7.70 (m, 2H), 7.40 (d, 1 H), 7.10-6.95 (m, 2H), 6.90-6.80 (m, 2H), 6.65 (d, 1 H), 5.15 (s, 2H), 3.95 (t, 2H), 3.75 (t, 2H), 3.50 (s, 3H), 2.40 (s, 3H), 2.10 (s, 3H), 2.05 (q, 4H), 1.90-1.70 (m, 4H), 1.60-1.50 (m, 2H), 0.60 (t, 6H).

(2) Preparation of 2-[5-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentyl]-isoindole- 1 ,3-dione

CF?H To a solution of 2-[5-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenoxy)-pentyl]-isoindole-1 ,3-dione (compound prepared in Example 124-(1 )) (72.0 mg, 0.01 mmol) in MeOH/CH2CI2(4/1 v/v, 2 ml) was added pTsOH(30.0 mg, 0.015 mmol) and the mixture was stirred at 60 degrees C for 12 h. The reaction mixture was concentrated under reduced pressure and the obtained residue was purified by silica gel chromatography (n-Hexane: EtOAc = 6:1 ) to give the title compound (61.5 mg, 91%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.85 (m, 2H), 7.70 (m, 2H), 7.40 (d, 1 H), 7.10-6.95 (m, 2H), 6.90-6.80 (m, 2H), 6.65 (d, 1 H), 4.10 (bs, 1 H), 3.95 (t, 2H), 3.75 (t, 2H), 2.35 (s, 3H), 2.10 (s, 3H), 2.05 (q, 4H), 1.90-1.70 (m, 4H), 1.60-1.50 (m, 2H), 0.60 (t, 6H). (3) Preparation of 4-(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-yn-2-ol

Using the same procedure as described for the preparation of Example 118-(2), the title compound was prepared from 2-[5-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-pr opyl}-2-methyl- phenoxy)-pentyl]-isoindole-1 ,3-dione (compound prepared in Example 124-(2)). The yield was 22%. 1H-NMR (300MHz, CDCI3): 7.30 (d, 1 H), 7.05 (bs, 1 H), 7.00-6.80 (m, 3H), 6.65 (d, 1 H), 4.70-4.50 (bs, 2H), 3.75 (t, 2H), 2.70 (t, 2H), 2.35 (s, 3H), 2.10 (s, 3H), 2.05 (q, 4H), 1.75-1.40 (m, 6H), 0.60 (t, 6H); MS (ESI-) : 542 ([M-HV).

Example 125 Preparation of (E)-4-(4-{1 -[4-(5-Amino-pentyloxy)-3-methyl-phenyl]-1 -ethyl- propyl}-2-methyl-phenyl)-1 ,1 ,1 -trifluoro-2-trifluoromethyl-but-3-en-2-ol

H2N

(1 ) Preparation of 2-[5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxy)-pentyl]-isoindole-1 ,3-dione

pOMOM ΌMOM

Using the same procedure as described for the preparation of Example 100-(1), the title compound was prepared from 4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phe nyl]-propyl}-2- methyl-phenol (compound prepared in Example 30-(1 )). The yield was 80%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.47-1.58 (m, 2H), 1.72-1.88 (m, 4H), 2.04 (q, 4H), 2.11 (s, 3H), 2.31 (s, 3H), 3.49 (s, 3H), 3.72 (t, 2H), 3.91 (t, 2H), 4.96 (s, 2H), 6.05 (d, 1 H), 6.65 (d, 1 H)1 6.85-7.02 (m, 4H), 7.31-7.36 (m, 2H), 7.69-7.71 (m, 2H), 7.82-7.85 (m, 2H).

(2) Preparation of 2-[5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydrox y-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentyl]-isoindole- 1 ,3-dione

Using the same procedure as described for the preparation of Example 55 (deprotection procedure of MOM group with TMSBr), the title compound was prepared from 2-[5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxy)-pentyl]-isoindole-1 ,3-dione (compound prepared in Example 125-(1)). The yield was 95%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 1.47-1.58 (m, 2H), 1.70-1.88 (m, 4H), 2.03 (q, 4H), 2.10 (s, 3H), 2.32 (s, 3H), 3.71 (t, 2H), 3.90 (t, 2H), 6.07 (d, 1 H), 6.64 (d, 1 H), 6.85-7.00 (m, 4H), 7.31-7.39 (m, 2H), 7.67-7.70 (m, 2H), 7.81-7.84 (m, 2H).

(3) Preparation of (E)-4-(4-{1-[4-(5-Amino-pentyloxy)-3~methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-1 ,1 ,1 -trifluoro-2-trifluoromethyl-but-3-en-2-ol

ΓF0H

Using the same procedure as described for the preparation of Example 118-(2), the title compound was prepared from 2-[5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-but-1-enyl)-phenyl]-pr opyl}-2-methyl- phenoxy)-pentyl]-isoindole-1 ,3-dione (compound prepared in Example 125-(2)). The yield was 32%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 1.47-1.58 (m, 4H), 1.73-1.81 (m, 2H), 2.04 (q, 4H), 2.13 (s, 3H), 2.31 (s, 3H), 3.71 (t, 2H), 3.90 (t, 2H), 6.08 (d, 1 H), 6.64 (d, 1 H), 6.86-7.02 (m, 4H), 7.31-7.38 (m, 2H); MS (ESI+) : 546 ([M+H]+).

Example 126 Preparation of 5(R)-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-pyrrolidin-2-one

OH

To a solution of 4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-phenyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 18) (300 mg, 0.78 mmol) in anhydrous CH3CN (7 ml) under nitrogen atmosphere were added K2CO3 (161 mg, 1.17 mmol) and (R)-toluene-4-sulfonic acid 5-oxo-pyrrolidin-2- ylmethyl ester (315 mg, 1.17 mmol) and the mixture was stirred at 100 degrees C overnight. The reaction mixture was cooled to room temperature, poured into sat. NH4CI aq. and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc- n-Hexane (1 :1 ) to give the title compound (200 mg, 53%). 1H NMR (CDCI3): 7.02 (d, 1 H), 6.93 (m, 4H), 6.63 (d, 1 H), 5.94 (s, NH), 4.08 (m, 1 H), 3.96 (dd, 1 H), 3.80 (dd, 1 H), 3.23 (dt, 1 H), 2.86 (m, 1 H), 2.55 (m, 1 H), 2.38 (m, 2H), 2.25 (s, 3H), 2.14 (s, 3H), 2.04 (q, 4H), 1.93 (m, 1 H), 1.79 (m, 1 H), 1.48 (m, 2H), 0.88 (s, 9H), 0.59 (t, 6H); MS (ESI+) : 502 ([M+Na]+).

Example 127 Preparation of 5(S)-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-pyrrolidin-2-one

OH Preparation of 5(S)-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-pyrrolidin-2-one

Using the same procedure as described for the preparation of Example 126, the title compound was prepared from 4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl- phenyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 18) and (S)-toluene-4-sulfonic acid 5-oxo-pyrrolidin-2-ylmethyl ester. The yield was 53%. 1H NMR (CDCI3): 7.02 (d, 1 H), 6.93 (m, 4H), 6.63 (d, 1 H), 5.94 (s, NH), 4.08 (m, 1 H)1 3.96 (dd, 1 H), 3.80 (dd, 1 H), 3.23 (dt, 1 H), 2.86 (m, 1 H), 2.55 (m, 1 H), 2.38 (m, 2H), 2.25 (s, 3H), 2.14 (s, 3H)1 2.04 (q, 4H), 1.93 (m, 1 H), 1.79 (m, 1 H), 1.48 (m, 2H), 0.88 (s, 9H), 0.59 (t, 6H); MS (ESI+) : 502 ([M+Na]+).

Example 128 Preparation of 4(R)-Amino-5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid

OH Preparation of 4(R)-Amino-5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid

OH OH

5(S)-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-m ethyl-phenyl]-propyl}-2- methyl-phenoxymethyl)-pyrrolidin-2-one (compound prepared in Example 126) (100 mg, 0.21 mmol) was dissolved in concentrated HCI (0.5 ml, 36wt% in water) and the mixture was stirred at reflux temperature overnight. The reaction mixture was concentrated under reduced pressure and the obtained residue was purified by ODS chromatography (CH3OH / H2O (0.1 %TFA) = 80 / 20) to give the title compound (25 mg, 24%). 1H NMR (CD3OD): 7.10-6.95 (m, 5H), 6.90 (d, 1 H), 4.28 (dd, 1 H), 4.14 (dd, 1 H), 3.76 (m, 1 H), 3.22 (dt, 1 H), 2.93 (m, 1 H)1 2.60 (m, 3H), 2.30 (s, 3H), 2.27 (s, 3H), 2.14 (m, 6H), 1.82 (m, 1 H), 1.55 (m, 1 H), 0.94 (s, 9H), 0.65 (t, 6H); MS (ESI+) : 498 ([M+H]+).

Example 129 Preparation of 4(S)-Amino-5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid

HO2C OH Preparation of 4(S)-Amino-5-(4-{1 -ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentanoic acid

HO2C. OH OH

Using the same procedure as described for the preparation of Example 128, the title compound was prepared from 5(S)-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl- pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-pyr rolidin-2-one (compound prepared in Example 127). The yield was 17%. 1H NMR (CD3OD): 7.10-6.95 (m, 5H), 6.90 (d, 1 H), 4.28 (dd, 1 H), 4.14 (dd, 1 H), 3.76 (m, 1 H), 3.22 (dt, 1 H), 2.93 (m, 1 H), 2.60 (m, 3H), 2.30 (s, 3H), 2.27 (s, 3H), 2.14 (m, 6H), 1.82 (m, 1 H), 1.55 (m, 1 H), 0.94 (s, 9H), 0.65 (t, 6H); MS (ESI+) : 498 ([M+H]+).

Example 130 Preparation of 1-(4-{1 -[4-((S )-2-Amino-3-hydroxy-propoxy)-3-methyl-phenyl]-1- ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol OH (1) Preparation of (S)-2,2-Dimethyl-4-(toluene-4-sulfonyloxymethyl)-oxazolidine - 3-carboxylic acid tert-butyl ester CO2Me ^-OH /"0Ts r~\ Γ \ Γ~\ O NBoc ► O NBoc ► O NBoc /\ ^\ /\ To a solution of (S)-2,2-Dimethyl-oxazolidine-3,4-dicarboxylic acid 3-tert-butyl ester 4-methyl ester (435 mg, 1.678 mmol) in THF (5 ml) under nitrogen atmosphere was added 1 N-LiAIH4 (5 ml, 5.033 mmol) at degrees C and the mixture was stirred at room temperature for 1 h. The mixture was quenched with water and 10% NaOH solution, filtered through celite. The filtrate was diluted with EtOAc and washed with brine, dried over MgSO4, filtered, and concentration in vacuo. The obtained residue was purified by flash chromatography eluting with 5:1 Hexane/Ethyl acetate to give the (R)-4-Hydroxymethyl-2,2-dimethyl- oxazolidine-3-carboxylic acid tert-butyl ester (383 mg, 99%) as a white solid. To a solution of (R)-4-Hydroxymethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (383 mg, 1.656 mmol) in anhydrous pyridine (4 ml) under nitrogen atmosphere was added tosyl chloride (631 mg, 3.312 mmol) at 0 degrees C and the mixture was stirred for 24 h. The reaction mixture was concentrated under reduced pressure and diluted with EtOAc, washed with brine, dried over MgSO4, filtered, and concentrated. Recrystallization from EtOAc-n-hexane to give the title compound (554 mg, 87%). 1H-NMR (300MHz, CDCI3): 1.40 (s, 9H), 1.54 (s, 3H), 2.45 (s, 3H), 3.78-4.20 (m, 5H), 7.40 (d, 2H), 7.81 (d, 2H); MS (ESI+) : 408 ([M+Na]+).

(2) Preparation of 4(R)-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-meth yl- pheny^-propylJ^-methyl-phenoxymethyl^^-dimethyl-oxazolidine- S-carboxylic acid tert-butyl ester HO A\oc To a solution of 4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyI- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 18) (110 mg, 0.288 mmol) in anhydrous DMF (3 ml) under nitrogen atmosphere were added Cs2CO3 (281 mg, 0.864 mmol) and (S)-2,2-Dimethyl-4-(toluene-4- sulfonyloxymethyl)-oxazolidine-3-carboxylic acid tert-butyl ester (compound prepared in Example 130-(1)) (167 mg, 0.432 mmol) and the mixture was stirred at 110 degrees C for 3 h. The reaction mixture was cooled to room temperature, poured into sat. NH4CI aq. and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :9) to give the title compound (169 mg, 77%) as a white solid. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 0.89 (s, 9H), 1.43-1.84 (m, 5H), 2.04 (q, 4H), 2.16 (s, 3H), 2.25 (s,3H), 2.50-2.61 (m, 1 H), 2.81-2.91 (m, 1 H), 3.27 (dd, 1 H), 3.78-3.93 (m, 1 H), 3.93-4.02 (m, 1 H), 6.82 (d, 1 H), 6.90-6.97 (m, 4H), 7.01 (d, 1 H).

(3) Preparation of 1-(4-{1-[4-((S)-2-Amino-3-hydroxy-propoxy)-3-methyl-phenyl]- 1-ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol

OH H2N

To a solution of 4(R)-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-meth yl- phenyl]-propyl}-2-methyl-phenoxymethyl)-2,2-dimethyl-oxazoli dine-3-carboxylic acid tert-butyl ester (compound prepared in Example 130-(2)) (148 mg, 0.248 mmol) in 1 ,4-dioxane (10 ml) was added cone. HCI (2 ml) at 0 degrees C and the mixture was stirred at room temperature for 4 h. The mixture was neutralized by sat. NaHCO3 solution, diluted with EtOAc, washed with brine, dried over MgSO-1, filtered, and concentration in vacuo. The obtained residue was chromatographed on amino functionalized silica gel with EtOAc to give the title compound (30 mg, 26.5%). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H)1 0.89 (s, 9H), 1.55 (m, 1 H), 1.75-1.84 (m, 1 H), 2.04 (q, 4H), 2.16 (s, 3H), 2.25 (s,3H), 2.55-2.57 (m, 1 H), 2.84-2.85 (m, 1 H), 3.23 (d, 1 H), 3.25-3.40 (m, 1 H), 3.60 (dd, 1 H), 3.75 (dd, 1 H), 3.91-3.98 (m, 2H), 6.70 (d, 1 H), 6.90-6.97 (m, 4H), 7.02 (d, 1 H) ; MS (ESI+) : 456 ([M+H]+).

Example 131 Preparation of 1 -(4-{1 -[4-((R)-2-Amino-3-hydroxy-propoxy)-3-methyl-phenyl]-1 - ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol

OH (1) Preparation of (R)-2,2-Dimethyl-4-(toluene-4-sulfonyloxymethyl)-oxazolidine - 3-carboxylic acid tert-butyl ester sC02Me ^-OTs ΓΛ O ΓΛ NBoc — O NBoc

Using the same procedure as described for the preparation of Example 130-(1 ), the title compound was prepared from (R)-2,2-Dimethyl-oxazolidine-3,4- dicarboxylic acid 3-tert-butyl ester 4-methyl ester. The yield was 49%. 1H-NMR (300MHz, CDCI3): 1.40 (m, 9H), 1.51 (s, 3H), 2.49 (s, 3H), 3.71-4.20 (m, 5H), 7.40 (d, 2H), 7.81 (d, 2H); MS (ESI+) : 408 ([M+H]+).

(2) Preparation of 4(S)-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-meth yl- phenyl]-propyl}-2-methyl-phenoxymethyl)-2,2-dimethyl-oxazoli dine-3-carboxylic acid tert-butyl ester

OH Using the same procedure as described for the preparation of Example 130-(2), the title compound was prepared from 4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl- pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 18). The yield was 78%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 0.89 (s, 9H), 1.43-1.84 (m, 5H), 2.04 (q, 4H), 2.16 (s, 3H), 2.25 (s,3H), 2.50-2.61 (m, 1 H), 2.81-2.91 (m, 1 H), 3.27 (dd, 1H), 3.78-3.93 (m, 1H), 3.93-4.02 (m, 1H), 6.82 (d, 1 H), 6.90-6.97 (m, 4H), 7.01 (d. 1 H).

(3) Preparation of 1-(4-{1-[4-((R)-2-Amino-3-hydroxy-propoxy)-3-methyl-phenyl]- 1-ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol

OH %,-§ OH

Using the same procedure as described for the preparation of Example 130-(3), the title compound was prepared from 4(S)-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxyme thyl)-2,2- dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (compound prepared in Example 131 -(2)). The yield was 59%. 1H-NMR (300MHz, CDCI3): 0.60 (t, 6H), 0.89 (s, 9H), 1.43-1.57 (m, 1H), 1.68- 1.84 (m, 4H), 2.04 (q, 4H), 2.16 (s, 3H), 2.25 (s,3H), 2.51-2.61 (m, 1H), 2.81- 2.91 (m, 1 H), 3.22 (dd, 1 H), 3.25-3.40 (m, 1 H), 3.61 (dd, 1 H), 3.75 (dd, 1 H), 3.91-3.98 (m, 2H), 6.68 (d, 1 H), 6.90-6.97 (m, 4H), 7.01 (d, 1 H); MS (ESI+) : 456 ([M+H]+).

Example 132 Preparation of 1 (R)-(4-{1 -[4-((R)-2-Amino-4-hydroxy-butoxy)-3-methyl-phenyl]-1 - ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol (1) Preparation of (R)-1-(tert-Butyl-dimethyl-silanyl)-4-hydroxymethyl-azetidin -2- one o

O A TBDMS * ςf Pk ^TBDMS To a solution of (R)-1-(tert-Butyl-dimethyl-silanyl)-4-oxo-azetidine-2-carbox ylic acid (800 mg, 3.49 mmol) in CH2CI2 (30 ml) were added BnOH (0.4 ml, 3.84 mmol), EDC (803 mg, 4.19 mmol), and DMAP (catalytic amount) and the mixture was stirred at room temperature overnight. The reaction mixture was poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc- n-Hexane (1 :40) to give (R)-1-(tert-Butyl-dimethyl-silanyl)-4-oxo-azetidine-2- carboxylic acid benzyl ester (954 mg, 86%). To a solution of CaCI2 (994 mg, 8.96 mmol) in EtOH (6 ml) and THF (12 ml) was added NaBH4 (567 mg, 14.9 mmol) at room temperature. To the mixture, (R)-1- (tert-Butyl-dimethyl-silanylH-oxo-azetidine^-carboxylic acid benzyl ester (954 mg, 2.97 mmol) was added and the mixture was stirred at 0 degrees C for 3 h. The reaction mixture was poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :5) to give the title compound (150 mg, 23%). 1H-NMR (300MHz, CDCI3): 0.23 (s, 3H), 0.26 (s, 3H), 0.94 (s, 9H), 1.74-1.84 (m, 1 H), 2.84 (dd, 1 H), 3.08 (dd, 1 H), 3.63-3.84 (m, 3H).

(2) Preparation of 1 -(tert-Butyl-dimethyl-silanyl)-4(R)-(4-{1 -ethyl-1 -[4-(3-hydroxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)-azetidin- 2-one ~JD"° ° VTBDMS To a solution of 4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 18) (140 mg, 0.65 mmol) were added triphenylphosphine (256 mg, 0.975 mmol), DEAD (0.15 ml, 0.975 mmol), and (R)-1-(tert-Butyl-dimethyl-silanyl)-4-hydroxymethyl- azetidin-2-one (compound prepared in Example 132-(1 )) (274mg, 0.715mmol) and the mixture was stirred at room temperature for 2days. The mixture was filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :7) to give the title compound (186 mg, 49%). 1H-NMR (300MHz, CDCI3): 0.23 (s, 3H), 0.26 (s, 3H), 0.59 (t, 6H), 0.89 (s, 9H), 0.94 (s, 9H), 1.39 (d, 1 H), 1.48-1.57 (m, 1 H), 1.74-1.84 (m, 1 H), 2.03 (q, 4H), 2.12 (s, 3H), 2.25 (s, 3H), 2.49-2.69 (m, 1 H), 2.98 (m, 1 H), 3.31-3.27 (m, 2H), 3.89-3.95 (m, 1H), 4.08-4.22 (m, 2H), 6.63 (d, 1H), 6.89-6.97 (m, 4H), 7.01 (d, 1 H); MS (ESI+) : 602 ([M+Na]+).

(3) Preparation of 2(R)-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-meth yl- phenyl]-propyl}-2-methyl-phenoxymethyl)-4-oxo-azetidine-1 -carboxylic acid tert- butyl ester

TBDMS 0 Boc

To a solution of 1-(tert-Butyl-dimethyl-silanyl)-4(R)-(4-{1-ethyl-1-[4-(3-hyd roxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)-azetidin- 2-one (compound prepared in Example 132-(2)) (184 mg, 0.317 mmol) in THF (3 ml) was added 1M TBAF in THF (0.48 ml, 0.48 mmol) and the mixture was stirred at room temperature for 2 h. The reaction mixture was poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was dissolved in CH2CI2 (3 ml). To the mixture, DMAP (catalytic amount), triethylamine (0.13 ml, 0.96 mmol), and (Boc)2O (95 mg, 0.42 mmol) were added and the mixture was stirred at room temperature overnight. The reaction mixture was poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :4) to give the title compound (127 mg, 71 %). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.47 (s, 9H), 1.48-1.57 (m, 1H), 1.74-1.84 (m, 1H), 2.03 (q, 4H), 2.14 (s, 3H), 2.25 (s, 3H), 2.50-2.60 (m, 1 H), 2.81-2.91 (m, 1 H), 3.12 (t, 2H), 3.24 (d, 1 H), 4.19-4.29 (m, 2H), 4.38 (dd, 1H), 6.68 (d, 1H), 6.89-6.97 (m, 4H), 7.01 (d, 1 H).

(4) Preparation of [1(R)-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyll-propylJ^-methyl-phenoxymethyO-S-hydroxy-propy ll-carbamic acid tert-butyl ester

O^ x\Boc 0H StHBoc ' ' OH To a solution of 2(R)-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-4-oxo-azetidine-1 -carboxylic acid tert- butyl ester (compound prepared in Example 132-(3)) (127 mg, 0.224 mmol) in THF (2 ml) was added 1 M LAH in THF (0.33 ml, 0.33 mmol) and the mixture was stirred at 0 degrees C for 30min. The reaction mixture was quenched with water and 10% NaOH, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc- n-Hexane (1 :3) to give the title compound (114 mg, 87%). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.45 (s, 9H), 1.48-1.57 (m, 1H), 1.73-1.89 (m, 3H), 2.03 (q, 4H), 2.16 (s, 3H), 2.25 (s, 3H), 2.50-2.60 (m, 1 H), 2.81-2.91 (m, 1 H), 3.21-3.26 (m, 1 H), 3.36 (m, 1 H), 3.71 (m, 2H), 3.91-3.95 (dd,1 H), 4.08-4.20 (m, 2H), 4.38 (dd, 1 H), 6.66 (d, 1 H), 6.88-6.98 (m, 4H), 7.01 (d, 1 H).

(5) Preparation of 1(R)-(4-{1-[4-((R)-2-Amino-4-hydroxy-butoxy)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan -3-ol

OH To a solution of [1 (R)-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methy l- phenyll-propyl^-methyl-phenoxymethyO-S-hydroxy-propyll-carba mic acid tert- butyl ester (compound prepared in Example 132-(4)) (111 mg, 0.195 mmol) in dioxane (2.5 ml) was added cone. HCI (1.1 ml) and the mixture was stirred at room temperature for 1 h. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with CH2CI2-MeOH (10:1 ) to give the title compound (50 mg, 54%). 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.43-1.57 (m, 1 H), 1.70- 1.89 (m, 3H), 2.03 (q, 4H), 2.17 (s, 3H), 2.25 (s, 3H), 2.50-2.60 (m, 1 H), 2.81- 2.91 (m, 1 H), 3.24 (d, 1 H), 3.31-3.40 (m, 1 H), 3.74 (m, 1 H), 3.85-3.91 (m,2H), 6.66 (d, 1H), 6.88-6.98 (m, 4H), 7.01 (d, 1H); MS (ESI+) : 470 ([M+H]+).

Example 133 Preparation of 1 (S)-(4-{1-[4-((S)-2-Amino-4-hydroxy-butoxy)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol

HO NH2 OH (1) Preparation of (S)-1-(tert-Butyl-dimethyl-silanyl)-4-hydroxymethyl-azetidin -2- one OH

θ' "TODMS Cf ~*SBDMS Using the same procedure as described for the preparation of Example 132-(1), the title compound was prepared from (S)-1-(tert-Butyl-dimethyl-silanyl)-4-oxo- azetidine-2-carboxylic acid. The yield was 88%. 1 H-NMR (300MHz, CDCI3): 0.23 (s, 3H), 0.26 (s, 3H), 0.94 (s, 9H), 1.74-1.84 (m, 1 H), 2.84 (dd, 1H), 3.08 (dd, 1H), 3.63-3.84 (m, 3H).

(2) Preparation of 1-(tert-Butyl-dimethyl-silanyl)-4(S)-(4-{1-ethyl-1-[4-(3-hyd roxy- 4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xymethyl)-azetidin- 2-one

' 0 r^ VB°DMS Using the same procedure as described for the preparation of Example 132-(2), the title compound was prepared from 4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl- pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 18) and (S)-1-(tert-Butyl-dimethyl-silanyl)-4-hydroxymethyl-azetidin -2- one (compound prepared in Example 133-(1 )). The yield was 19%. 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.39 (d, 1 H), 1.48-1.57 (m, 1 H), 1.57 (s, 15H), 1.74-1.84 (m, 1 H), 2.04 (q, 4H)1 2.15 (s, 3H), 2.25 (s, 3H), 2.50-2.60 (m, 1 H), 2.81-2.91 (m, 2H), 3.11-3.18 (dd, 1 H), 3.21-3.27 (dd, 1 H), 3.93-3.98 (dd, 1 H), 4.02-4.07 (m, 1 H), 4.11-4.16 (m, 1 H), 6.66 (d, 1 H), 6.89-6.97 (m, 4H), 7.01 (d, 1 H); MS (ESI+) : 602 ([M+Na]+).

(3) Preparation of 2(S)-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-meth yl- phenyll-propylJ^-methyl-phenoxymethylH-oxo-azetidine-i-carbo xylic acid tert- butyl ester -N o OH TBDMS O Boc Using the same procedure as described for the preparation of Example 132-(3), the title compound was prepared from 1-(tert-Butyl-dimethyl-silanyl)-4(S)-(4-{1- ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2-methyl- phenoxymethyl)-azetidin-2-one (compound prepared in Example 133-(2)). The yield was 67% 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.47 (s, 9H), 1.48-1.57 (m, 1H), 1.72-1.84 (m, 1 H), 2.02 (q, 4H), 2.14 (s, 3H), 2.25 (s, 3H), 2.50-2.60 (m, 1 H), 2.81-2.91 (m, 1 H), 3.12 (t, 2H), 3.22 (d, 1 H), 4.19-4.29 (m, 2H), 4.38 (dd, 1 H)1 6.68 (d, 1 H), 6.89-6.94 (m, 4H), 7.01 (d, 1 H).

(4) Preparation of [1 (S)-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-3-hydroxy-pro pyl]-carbamic acid tert-butyl ester

OH

Using the same procedure as described for the preparation of Example 132-(4), the title compound was prepared from 2(S)-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxyme thyl)-4-oxo- azetidine-1-carboxylic acid tert-butyl ester (compound prepared in Example 133- (3)). The yield was 84% 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H), 0.89 (s, 9H), 1.45 (s, 9H), 1.48-1.57 (m, 1 H), 1.73-1.89 (m, 3H), 2.03 (q, 4H), 2.16 (s, 3H), 2.25 (s, 3H), 2.50-2.60 (m, 1H), 2.81-2.91 (m, 1 H), 3.22 (d, 1H), 3.39 (m, 1H), 3.71 (m, 2H), 3.91-3.95 (dd,1 H), 4.08-4.20 (m, 2H), 4.38 (dd, 1 H)1 6.66 (d, 1 H), 6.88-6.98 (m, 4H), 7.01 (d, 1 H). (5) Preparation of 1 (S)-(4-{1-[4-((S)-2-Amino-4-hydroxy-butoxy)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan -3-ol

HO. OH NH2 ' ' OH Using the same procedure as described for the preparation of Example 132-(5), the title compound was prepared from [1(S)-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxyme thyl)-3-hydroxy- propyl]-carbamic acid tert-butyl ester (compound prepared in Example 133-(4)). The yield was 42% 1H-NMR (300MHz, CDCI3): 0.59 (t, 6H)1 0.89 (s, 9H), 1.45-1.54 (m, 1 H)1 1.73- 1.83 (m, 3H), 2.03 (q, 4H), 2.18 (s, 3H), 2.24 (s, 3H), 2.28-2.37 (m, 2H), 2.50- 2.60 (m, 1 H), 2.81-2.91 (m, 1 H), 3.24 (m, 1 H), 3.84-4.03 (m, 2H), 4.24-4.29 (m, 1H), 4.45-4.51 (m,1H), 6.69 (d, 1H), 6.88-6.95 (m, 4H), 7.01 (d, 1H); MS (ESI+) : 470 ([M+H∏.

Example 134 Preparation of 4-[2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenyl)-ethanesulfonyl]-butyric acid

OH (1) Preparation of Trifluoro-methanesulfonic acid 4-{1-[4-(4,4-dimethyl-3-oxo- pentyl)-3-methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl ester

TfO O 1 1 O To a solution of 1-{4-[1-Ethyl-1-(4-hydroxy-3-methyl-phenyl)-propyl]-2-methyl - phenyl}-4,4-dimethyl-pentan-3-one (compound prepared in Example 18-(3)) (6.4 g, 16.8 mmol) in CH2CI2 (100 ml) were added Tf2O (4.2 ml, 25.2 mmol) and pyridine (4.1 ml, 50.4 mmol) at 0 degrees C under N2 atmosphere and the mixture was stirred at room temperature for 5 h. The reaction mixture was poured into sat. NaHCO3 and the products were extracted with CH2CI2. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane: EtOAc (50:1) to give the title compound (7.25 g, 84%). 1H-NMR (300MHz, CDCI3): 0.60 (6H, t), 1.08 (9H, s), 2.05 (4H, q), 2.27 (3H, s), 2.31 (3H, s), 2.69-2.76 (2H, m), 2.80-2.88 (2H, m), 6.84-6.89 (2H, m), 6.96-7.10 (4H, m).

(2) Preparation of 1-{4-[1-(4-Allyl-3-methyl-phenyl)-1-ethyl-propyl]-2-methyl- phenyl}-4,4-dimethyl-pentan-3-one

TfO ' O I I o To a solution of Trifluoro-methanesulfonic acid 4-{1-[4-(4,4-dimethyl-3-oxo- pentyl)-3-methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl ester (compound prepared in Example 134-(1)) (7.25 g, 14.15 mmol) in DMF (70 ml) under argon atmosphere were added allyltributyltin (17.55 ml, 56.59 mmol), PdCI2(PPh3)2 (993 mg, 1.415 mmol), PPh3 (742 mg, 2.830 mmol) and LiCI (5.04 g, 119 mmol) and the mixture was stirred at 140 degrees C for 3 h. The mixture was quenched with sat. NH4CI aq. and filtered through celite. The filtrate was poured into water and the products were extracted with diethyleter. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n- Hexane:EtOAc (50:1 ) to give the title compound (4.79 g, 84%). 1H-NMR (300MHz, CDCI3): 0.59 (6H, t), 1.10 (9H, s), 2.06 (4H, q), 2.22 (3H, s), 2.26 (3H, s), 2.69-2.78 (2H, m), 2.80-2.87 (2H, m), 3.33 (2H, d), 4.95-5.05 (2H, m), 5.88-6.02 (1 H, m), 6.88-7.00 (6H, m).

(3) Preparation of 1-{4-[1-(4-Allyl-3-methyl-phenyl)-1-ethyl-propyl]-2-methyl- phenyl}-4,4-dimethyl-pentan-3-ol O ' ' OH To a solution of 1-{4-[1-(4-Allyl-3-methyl-phenyl)-1-ethyl-propyl]-2-methyl- phenyl}-4,4-dimethyl-pentan-3-one (compound prepared in Example 134-(2)) (4.79 g, 11.84 mmol) in EtOH (100 ml) was added NaBH4 (537 mg, 14.21 mmol) at 0 degrees C and the mixture was stirred at room tempareture for 3 h. The reaction mixture was quenched with water and poured into sat. NH4CI aq and the products were extracted with EtOAc. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane:EtOAc (20:1 ) to give the title compound (2.7 g, 56%). 1H-NMR (300MHz, CDCI3): 0.60 (6H, t), 0.90 (9H, s), 1.45-1.59 (1 H, m), 1.74- 1.85 (1H, m), 2.07 (4H, q), 2.23 (3H, s), 2.28 (3H, s), 2.51-2.60 (1H, m), 2.80- 2.90 (1 H, m), 3.22-3.29 (1 H, m), 3.32 (2H, d), 4.85-5.08 (2H, m), 5.90-6.02 (1 H, m), 6.89-7.03 (6H, m).

(4) Preparation of [1-(2-{4-[1-(4-Allyl-3-methyl-phenyl)-1-ethyl-propyl]-2-meth yl- phenyl}-ethyl)-2,2-dimethyl-propoxy]-triethyl-silane

OH ' ' 0TES To a stirred solution of 1-{4-[1-(4-Allyl-3-methyl-phenyl)-1-ethyl-propyl]-2- methyl-phenyl}-4,4-dimethyl-pentan-3-ol (compound prepared in Example 134- (3)) (1.40 g, 3.44 mmol) in anhydrous DMF (11.5 ml) were added Et3SiCI (0.69 ml, 4.12mmol) and imidazole (585 mg, 8.59 mmol) at 0 degrees C under N2 atmosphere and the mixture was stirred at room temperature for 16 h. The reaction mixture was poured into water and the products were extracted with EtOAc. The extracts were washed with 1 N HCI, sat. NaHCO3 and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane:EtOAc (30:1) to give the title compound (1.79 g, 100%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.05-6.85 (m, 6H), 6.00-5.90 (m, 1 H), 5.10-4.90 (m, 2H), 3.40-3.30 (m, 3H), 2.85-2.70 (m, 1H), 2.50-2.40 (m, 1H), 2.25 (s, 3H), 2.20 (s, 3H), 2.05 (q, 4H), 1.85-1.70 (m, 1 H), 1.55-1.40 (m, 1 H), 1.05-0.90 (m, 15H), 0.70-0.50 (m, 15H).

(5) Preparation of 2-(4-{1-[4-(4,4-Dimethyl-3-triethylsilanyloxy-pentyl)-3-meth yl- phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-ethanol

OTES ' ' OTES To a stirred solution of [1-(2-{4-[1-(4-Allyl-3-methyl-phenyl)-1-ethyl-propyl]-2- methyl-phenyl}-ethyl)-2,2-dimethyl-propoxy]-triethyl-silane (compound prepared in Example 134-(4)) (1.79 g, 3.44 mmol) in Acetone/tBuOH/Water (4/1/1 v/v, 96 ml) were added NMO (1.01 g, 8.62 mmol) and OsO4(2.5%w/w in tBuOH, 4.30 ml, 10 mol%) at room temp, under N2 atmosphere. After stirring for 12.0 h, the reaction mixture was quenched with sat. NaHCO3 aq. and stirred for additionally 20 min. The reaction mixture was extracted with EtOAc. Resulted organic layer was washed with brine and dried over anhydrous Na2SO4, filtered, and evaporated under reduced pressure. The obtained residue was dissolved in EtOH/Water (1/1 v/v, 82 ml). To the solution, NaIO4 (866 mg, 4.05 mmol) and NaBH4 (460 mg, 12.2 mmol) was added and the mixture was stirred at 0 degrees C for 30 min. The reaction mixture was poured into sat. NH4CI aq. and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane: EtOAc (10:1) to give the title compound (1.33 g, 74%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.05-6.85 (m, 6H), 3.90-3.80 (m, 2H), 3.40 (dd, 1 H), 2.90-2.70 (m, 3H), 2.50-2.40 (m, 1H), 2.30 (s, 3H), 2.25 (s, 3H), 2.05 (q, 4H), 1.85-1.70 (m, 1 H), 1.55-1.40 (m, 1 H), 1.00 (t, 9H), 0.90 (t, 9H), 0.60 (t, 6H).

(6) Preparation of {1-[2-(4-{1-[4-(2-Bromo-ethyl)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-ethyl]-2,2-dimethyl-propoxy}-trieth yl-silane OTES OTES To a stirred solution of 2-(4-{1-[4-(4,4-Dimethyl-3-triethylsilanyloxy-pentyl)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-θthanol (compound prepared in Example 134-(5)) (1.33 g, 2.54 mmol) in CH2CI2 (8.5 ml) were added CBr4 (1.05 g, 3.18 mmol) and PPh3 (999 mg, 3.80 mmol) at 0 degrees C under N2 atmosphere. After stirring for 30min., the reaction mixture was evaporated under reduced pressure and the obtained residue was purified by silica gel column chromatography (n-Hexane:Acetone=20:1) to give the title compound (829 mg, 54%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.05-6.85 (m, 6H), 3.50 (t, 3H), 3.40 (dd, 1 H), 3.15 (t, 2H), 2.85-2.70 (m, 1H), 2.50-2.35 (m, 1H), 2.25 (s, 3H), 2.20 (s, 3H), 2.05 (q, 4H), 1.85-1.70 (m, 1 H), 1.55-1.40 (m, 1 H), 1.00 (t, 9H), 0.90 (t, 9H), 0.60 (t, 6H).

(7) Preparation of 1-(4-{1-[4-(2-Bromo-ethyl)-3-methyl-phenyl]-1-ethyl-propyl}- 2- methyl-phenyl)-4,4-dimethyl-pentan-3-ol

OTES To a stirred solution of {1-[2-(4-{1-[4-(2-Bromo-ethyl)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-ethyl]-2,2-dimethyl-propoxy}-trieth yl-silane (compound prepared in Example 134-(6)) (1.00 g, 1.70 mmol) in CH3CN (17 ml) was added 1 N HCI (1.7 ml) at room temperature. After stirring for 3.0 h, the reaction mixture was poured into water and the products were extracted with EtOAc. The extracts were washed with sat. NaHCO3 aq., dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane: EtOAc (7:1) to give the title compound (735 mg, 91%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.05-6.85 (m, 6H), 3.50 (t, 3H), 3.25 (m, 1H), 3.15 (t, 2H), 2.90-2.80 (m, 1 H), 2.60-2.50 (m, 1 H), 2.25 (s, 6H), 2.05 (q, 4H), 1.85-1.70 (m, 1 H), 1.55-1.40 (m, 1 H), 0.90 (t, 9H), 0.60 (t, 6H). (8) Preparation of 4-Mercapto-butyric acid methyl ester o *► HSv^-^^CO2Me

To a stirred solution of Dihydro-thiophen-2-one (2.06 g, 20.2 mmol) in 70.0 ml_ of MeOH was added Et3N (4.67 ml, 33.5 mmol) and refluxed for 24 h. The reaction mixture was evaporated under reduced pressure to give the title compound (2.50 g, 92.3%). 1H-NMR (300MHz, CDCI3): 3.70 (s, 3H), 2.60 (m, 2H), 2.48 (t, 2H), 1.95 (m, 2H).

(9) Preparation of 4-[2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenyl)-ethylsulfanyl]-butyric acid ethyl ester

EtO. Υ ~ a ~ T T OH ° ' I OH To a stirred solution of 1-(4-{1-[4-(2-Bromo-ethyl)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol (compound prepared in Example 134-(7)) (360 mg, 0.76 mmol) and 4-Mercapto-butyric acid methyl ester (compound prepared in Example 134-(8)) (204 mg, 1.52 mmol) in 3.80 ml of anhydrous DMF was added J-Pr2EtN (0.20 ml, 1.15 mmol) under N2 atmosphere at room temperature. The reaction mixture was stirred for 18 h at room temperature. The reaction mixture was concentrated under reduced pressure and the obtained residue was purified by silica gel chromatography (n- Hexane:EtOAc = 10:1) to give the title compound (48.5 mg, 12%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.05-6.85 (m, 6H), 3.70 (s, 3H), 3.25 (d, 1 H), 2.90- 2.50 (m, 10H), 2.25 (s, 6H), 2.05 (q, 4H), 1.85-1.75 (m, 1H), 1.55-1.40 (m, 1H), 0.90 (s, 9H), 0.60 (t, 6H).

(10) Preparation of 4-[2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenyl)-ethanesulfonyl]-buty ric acid ethyl ester O I I OH O O ' I OH To a stirred solution of 4-[2-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenyl)-ethylsulfanyl]-butyr ic acid ethyl ester (compound prepared in Example 134-(9)) (100 mg, 0.19 mmol) in 2.00ml of CH2CI2 was added mCPBA (144 mg, 0.48 mmol) at 0 degrees C and gradually warmed up to room temperature. The reaction mixture was stirred for 3.0 h at room temperature. The reaction mixture was poured into Na2S2θ3 aq. and the products were extracted with CH2CI2. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane: EtOAc (4:1) to give the title compound (103 mg, 99%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.05-6.85 (m, 6H), 3.70 (s, 3H), 3.30-3.00 (m, 7H), 2.95-2.80 (m, 1 H), 2.65-2.50 (m, 3H), 2.30 (s, 3H), 2.25 (s, 3H), 2.20-2.05 (m, 6H), 1.85-1.75 (m, 1 H), 1.60-1.45 (m, 1 H), 0.90 (s, 9H), 0.60 (t, 6H).

(11 ) Preparation of 4-[2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenyl)-ethanesulfonyl]-buty ric acid

OH O O To a stirred solution of 4-[2-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenyl)-ethanesulfonyl]-buty ric acid ethyl ester (compound prepared in Example 134-(1O)) (103 mg, 0.18 mmol) in 2.50 ml of Dioxane/Water (4/1 v/v) was added NaOH (14.4 mg, 0.36 mmol) at room temperature. The reaction mixture was stirred for 2.5 h at room temperature. The reaction mixture was poured into 1 N HCI and extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4., filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane: EtOAc (1 :1) to give the title compound (44.1 mg, 45%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.05-6.85 (m, 6H), 3.30-3.00 (m, 7H), 2.90-2.75 (m, 1 H), 2.60-2.40 (m, 3H), 2.20 (s, 6H), 2.20-2.05 (m, 6H), 1.85-1.70 (m, 1 H), 1.55- 1.40 (m, 1 H), 0.90 (s, 9H), 0.60 (t, 6H); MS (ESI-) : 543 ([M-H]").

Example 135 Preparation of 3-[2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenyl)-ethanesulfonyl]-propionic acid

OH (1 ) Preparation of 3-[2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenyl)-ethylsulfanyl]-propionic acid methyl ester

MeO

Using the same procedure as described for the preparation of Example 134-(9), the title compound was prepared from 1-(4-{1-[4-(2-Bromo-ethyl)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan -3-ol (compound prepared in Example 134-(7)) and Methyl 3-mercaptopropionate. The yield was 36%. 1H-NMR (300MHz, CDCI3): 7.05-6.85 (m, 6H), 3.70 (s, 3H)1 3.25 (d, 1 H), 2.90- 2.50 (m, 10H)1 2.25 (s, 6H), 2.05 (q, 4H), 1.85-1.70 (m, 1 H), 1.55-1.40 (m, 1 H), 0.90 (t, 9H), 0.60 (t, 6H); MS (ESI+) : 535 ([M+Na]+).

(2) Preparation of 3-[2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenyl)-ethanesulfonyl]-propionic acid methyl ester

MeO' MeO OH Using the same procedure as described for the preparation of Example 134- (10), the title compound was prepared from 3-[2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4 ,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenyl)-e thylsulfanyl]- propionic acid methyl ester (compound prepared in Example 135-(1)). The yield was 91%. 1H-NMR (300MHz, CDCI3): 7.05-6.85 (m, 6H), 3.70 (s, 3H), 3.30-3.10 (m, 7H), 2.90-2.75 (m, ,3H), 2.65-2.50 (m, 1H), 2.30 (s, 3H), 2.25 (s, 3H), 2.05 (q, 4H), 1.85-1.70 (m, 1 H), 1.55-1.40 (m, 1 H), 0.90 (t, 9H), 0.60 (t, 6H); MS (ESI+) : 567 ([M+Na]+).

(3) Preparation of 3-[2-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-meth yl- phenyl]-propyl}-2-methyl-phenyl)-ethanesulfonyl]-propionic acid

MeO' OH OH Using the same procedure as described for the preparation of Example 134- (11), the title compound was prepared from 3-[2-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenyl)-e thanesulfonyl]- propionic acid methyl ester (compound prepared in Example 135-(2)). The yield was 19%. 1H-NMR (300MHz1 CDCI3); 7.05-6.85 (m, 6H), 3.30-3.15 (m, 6H), 3.10-3.00 (m, 2H), 2.90-2.75 (m, 3H), 2.65-2.50 (m, 1 H), 2.25 (s, 6H), 2.05 (m, 4H), 1.85-1.70 (m, 1 H), 1.55-1.40 (m, 1 H), 0.90 (t, 9H), 0.60 (t, 6H); MS (ESI-) : 529 ([M-H]").

Example 136 Preparation of N-tert-Butyl-2-(4-{1 -[4-((S)-2,3-dihydroxy-propoxy)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-acetamide

HO-'VO HO (1 ) Preparation of 4-{1-[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenol

^OH To a solution of 3,3-bis[4-hydroxy-3-methylphenyl]pentane (1 g, 3.52 mmol) in DMSO (9 ml) was added t-BuOK (379 mg, 3.38 mmol) at room temperature under N2 atmosphere. After 5min., (S)-(+)-2,2-dimethyl 1 ,3-dioxolan-4-yl-methyl- p-toluenesulfonate (796 mg, 2.78 mmol) was added and the reaction mixture was stirred at 60 degrees C for 12 h. Then the reaction mixture was poured into sat. NH4CI and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n- Hexane:Acetone (20:1) to give the title compound (472 mg, 42.6%) as a white amorphous. 1H-NMR (300MHz, CDCI3): 7.00-6.80 (m, 4H), 6.80-6.60 (m, 2H), 4.90 (s, 1H), 4.55-4.45 (m, 1H), 4.20-3.90 (m, 4H), 2.10, 2.20(S, 6H), 2.10-1.90 (m, 4H), 1.49 (s, 3H), 1.48 (s, 3H), 0.60 (t, 6H).

(2) Preparation of Trifluoro-methanesulfonic acid 4-{1 -[4-((R)-2,2-dimethyl- [1 ,3]dioxolan-4-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2- methyl-phenyl ester

To a stirred solution of 4-{1-[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenol (compound prepared in Example 136-(1)) (18.6 g, 46.7 mmol) in CH2CI2 (460 ml) were added Tf2O (11.8 ml, 70.1 mmol) and pyridine (7.6 ml, 93.4 mmol) and the mixture was stirred at 0degrees C under N2 atmosphere for 1 h. Then the reaction mixture was poured into sat. NaHCO3 and the products were extracted with CH2CI2. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n- Hexane:Acetone (10:1) to give the title compound (14.5 g, 85%) as yellow oil. 1H-NMR (300MHz, CDCI3): 7.00-7.15 (m, 3H), 6.80-7.00 (m, 2H), 6.70 (d, 1 H), 4.45-4.55 (m, 1 H), 4.15 (m, 1 H), 4.05 (m, 1 H), 3.90-4.00 (m, 1 H), 2.35 (s, 3H), 2.15 (s, 3H), 2.05 (q, 4H), 1.50 (s, 3H), 1.40 (s, 3H), 0.60 (t, 6H). (3) Preparation of (R)-4-{4-[1-(4-Allyl-3-methyl-phenyl)-1-ethyl-propyl]-2-meth yl- phenoxymethyl}-2,2-dimethyl-[1 ,3]dioxolane

OTf

To a stirred solution of Trifluoro-methanesulfonic acid 4-{1 -[4-((R)-2,2-dimethyl- [1 ,3]dioxolan-4-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2- methyl-phenyl ester (compound prepared in Example 136-(2)) (8.52 g, 16.1 mmol) in DMF (80 ml) were added Pd2CI2(PPh3)2 (1.13 g, 10 mol%), PPh3 (842 mg, 20 mol%) and LiCI (5.72 g, 135 mmol) at room temperature under N2 atmosphere. After stirred for 10min., allyltributyltin (19.9 ml, 64.2 mmol) was added to the reaction mixture and stirred at 130 degrees C for 6 h. The reaction mixture was cooled to room temperature, poured into 1 N HCI and the products were extracted with diethylether. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane:EtOAc (20:1) to give the title compound (6.08 g, 90%) as colorless oil. 1H-NMR (300MHz, CDCI3): 7.05-6.90 (m, 5H), 6.70 (d, 1 H), 6.05-5.85 (m, 1 H), 5.05-4.90 (m, 2H), 4.50 (m, 1 H), 4.15 (m, 1 H), 4.05 (m, 1 H), 4.00-3.85 (m, 2H), 3.35 (d, 2H), 2.20 (s, 3H), 2.15 (s, 3H), 2.05 (q, 4H), 1.50 (s, 3H), 1.40 (s, 3H), 0.60 (t, 6H).

(4) Preparation of 2-(4-{1-[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-ethanol

To a stirred solution of (R)-4-{4-[1 -(4-Allyl-3-methyl-phenyl)-1 -ethyl-propyl]-2- methyl-phenoxymethyl}-2,2-dimethyl-[1 ,3]dioxolane (compound prepared in Example 136-(3)) (5.14 g, 12.2 mmol) in 336ml of Acetone/t-BuOH/Water (4/1/1 v/v) were added NMO (3.57 g, 30.5 mmol) and OsO4 (2.5% w/w in t-BuOH, 15.2 ml, 10 mol%) at room temperature under N2 atmosphere and the mixture was stirred for 12 h. The mixture was poured into sat. NaHCO3 and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to give 6.18 g of crude diol compound. The obtained crude diol compound (6.18 g) was dissolved in 274 ml of EtOH/Water (1/1 v/v). Then NaIO4 (2.89 g, 13.5 mmol) was added to the reaction mixture at 0 degrees C and followed the addition of NaBH4 (1.54 g, 13.5 mmol) portion wise. The reaction mixture was stirred for 30min and poured into sat. NH4CI and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n- Hexane:EtOAc (5:1) to give the title compound (3.46 g, 67%) as yellowish oil. 1H-NMR (300MHz, CDCI3): 7.05-6.90 (m, 5H), 6.70 (d, 1H), 4.45 (m, 1H), 4.15 (m, 1 H), 4.05 (m, 1 H), 4.00-3.85 (m, 2H), 3.70 (t, 2H), 2.85 (t, 2H), 2.30 (s, 3H), 2.15 (s, 3H), 2.05 (q, 4H), 1.50 (s, 3H), 1.40 (s, 3H), 0.60 (t, 6H).

(5) Preparation of (4-{1-[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-acetic acid

,CO2H -Λ-o l l _A-o I I

To a stirred solution of 2-(4-{1-[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)- 3-methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-ethanol (compound prepared in Example 136-(4)) (1.34 g, 3.14 mmol) in CH3CN (15 ml) and NaH2PO4 buffer solution (0.67M, 11.4 ml) were added TEMPO (34.3 mg, 0.22 mmol), NaOCI2 (710 mg, 6.28 mmol) in water (3 ml) and NaOCI (0.00387 ml, 2 mol%). The reaction mixture was stirred for 4.0 h at 35 degrees C. The mixture was poured into sat. NaHCO3 and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane: EtOAc (5:1 ) to give the title compound (1.21 g, 95%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.05 (m, 1 H), 7.00-6.90 (m, 4H), 6.70 (d, 1 H), 4.45 (m, 1H), 4.15 (m, 1H), 4.05 (m, 1H), 4.00-3.90 (m, 2H), 3.60 (s, 2H), 2.25 (s, 3H), 2.15 (s, 3H), 2.05 (q, 4H), 1.45 (s, 3H), 1.40 (s, 3H), 0.60 (t, 6H).

(6) Preparation of N-tert-Butyl-2-(4-{1-[4-((R)-2,2-dimethyl-[1 ,3]dioxolan-4- ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl) -acetamide

CO2H

To a stirred solution of (4-{1-[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-acetic acid (compound prepared in Example 136-(5)) (530 mg, 1.20 mmol) in anhydrous DMF (9.3 ml) were added t-BuNH2 (263 mg, 3.60 mmol), EDC (345 mg, 1.80 mmol), HOBT (243 mg, 1.80 mmol) and J-Pr2EtN (0.31 ml, 3.60 mmol) at 0 degrees C and the mixture was stirred at room temperature overnight. The reaction mixture was poured into water and the products were extracted with EtOAc. The extracts were washed with 1 N HCI, sat. NaHCO3 aq. and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane:Acetone (4:1) to give the title compound (525 mg, 88%) as a white amorphous. 1H-NMR (300MHz, CDCI3): 7.05-6.90 (m, 4H), 6.85 (m, 1 H), 6.70 (d, 1 H), 5.05 (bs, 1 H), 4.50 (m, 1 H), 4.15 (m, 1 H), 4.05 (m, 1 H)1 4.00-3.90 (m, 2H), 3.50 (s, 2H), 2.25 (s, 3H), 2.15 (s, 3H), 2.05 (q, 4H), 1.45 (s, 3H), 1.40 (s, 3H), 1.25 (s, 9H), 0.60 (t, 6H); MS (ESI+) : 496 ([M+H]+).

(7) Preparation of N-tert-Butyl-2-(4-{1-[4-((S)-2,3-dihydroxy-propoxy)-3-methyl - phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-acetamide To a stirred solution of N-tert-Butyl-2-(4-{1-[4-((R)-2,2-dimethyl-[1 ,3]dioxolan-4- ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl) -acetamide (compound prepared in Example 136-(6)) (525 mg, 1.06 mmol) in THF/H2O (5/1 v/v, 4.9 ml) was added TFA (0.82 ml, 10.6 mmmol) at 0 degrees C under N2 atmosphere and the mixture was stirred at room temperature for 5 h. The mixture was poured into sat. NaHCO3 aq. and the products were extracted with CH2CI2. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane:EtOAc (1 :1) to give the title compound (233 mg, 48%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.05-6.90 (m, 4H), 6.85 (m, 1 H), 6.70 (d, 1 H), 5.05 (bs, 1 H), 4.15 (m, 1 H), 4.05 (m, 2H), 4.00-3.90 (m, 2H), 3.50 (s, 2H), 2.60 (d, 1 H), 2.25 (s, 3H), 2.15 (s, 3H), 2.05 (m, 5H), 1.25 (s, 9H), 0.60 (t, 6H); MS (ESI+) : 456 ([M+H]+).

Example 137 Preparation of (4-{1 -[4-((S)-2,3-Dihydroxy-propoxy)-3-methyl-phenyl]-1 -ethyl- propyl}-2-methyl-phenyl)-acetic acid tert-butyl ester

HOVO HO (1 ) Preparation of (4-{1-[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-acetic acid tert-butyl ester

CO2H

To a stirred solution of (4-{1-[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-acetic acid (compound prepared in Example 136-(5)) (408 mg, 0.93 mmol) in CH2CI2 (9,3 ml) were added t-BuOH (207 mg, 2.79 mmol), DCC (230 mg, 1.11 mmol) and DMAP (11.4 mg, 10 mol%) at 0 degrees C and the mixture was stirred at room temperature overnight. The reaction mixture was poured into water and the products were extracted with EtOAc. The extracts were washed with 1 N HCI, sat. NaHCO3aq. and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane:Acetone (5:1) to give the title compound (217 mg, 47%) as a white amorphous. 1H-NMR(300MHz, CDCI3): 7.05-6.85 (m, 6H), 6.65 (d, 1 H), 4.50 (m, 1H), 4.20 (m, 1 H), 4.05 (m, 1 H), 4.00-3.90 (m, 2H), 3.50 (s, 2H), 2.25 (s, 3H), 2.15 (s, 3H), 2.05 (q, 4H), 1.45 (s, 3H), 1.40 (s, 12H), 0.60 (t, 6H); MS (ESI+) : 514 ([M+NH4]+).

(2) Preparation of (4-{1-[4-((S)-2,3-Dihydroxy-propoxy)-3-methyl-phenyl]-1-ethy l- propyl}-2-methyl-phenyl)-acetic acid tert-butyl ester

o-V-o^f HoΥ^o HO

Using the same procedure as described for the preparation of Example 136-(7), the title compound was prepared from (4-{1-[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4- ylmethoxy)-3-methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-acetic acid tert- butyl ester (compound prepared in Example 137-(1)). The yield was 75%. 1H-NMR (300MHz, CDCI3): 7.05 (m, 1 H), 7.00-6.90 (m, 4H), 6.65 (d, 1 H), 4.50 (m, 1 H), 4.15 (m, 1 H), 4.05 (m, 1 H), 3.90-3.70 (m, 2H), 3.50 (s, 2H), 2.75 (d, 1 H), 2.25 (s, 3H), 2.15 (s, 3H), 2.05 (m, 5H), 1.40 (s, 9H), 0.60 (t, 6H); MS (ESI+) : 474 ([M+NH4]+).

Example 138 Preparation of 3-[4-(1-Ethyl-1 -{3-methyl-4-[2-(2-methyl-propane-2-sulfinyl)-ethyl]- phenyl}-propyl)-2-methyl-phenoxy]-propane-1 ,2(S)-diol HθΥ~<> HO (1) Preparation of (R)-4-(4-{1-[4-(2-Bromo-ethyl)-3-methyl-phenyl]-1-ethyl- propyl}-2-methyl-phenoxymethyl)-2,2-dimethyl-[1 ,3]dioxolane

To a stirred solution of 2-(4-{1 -[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)- 3-methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-ethanol (compound prepared in Example 136-(4)) (2.51 g, 5.88 mmol) in 20 ml of CH2CI2 were added CBr4 (2.44 g, 7.36 mmol) and PPh3 (2.31 g, 8.81 mmol) at 0 degrees C under N2 atmosphere. After stirred for 30min., the reaction mixture was evaporated under reduced pressure and the obtained residue was purified by silica gel chromatography (n-Hexane:Acetone=10:1 ) to give the title compound (2.76 g, 96%) as yellowish oil. 1H-NMR (300MHz, CDCI3): 7.05-6.90 (m, 5H), 6.70 (d, 1 H), 4.45 (m, 1 H), 4.15 (m, 1 H), 4.05 (m, 1 H), 4.00-3.85 (m, 2H), 3.50 (t, 2H), 3.10 (t, 2H), 2.25 (s, 3H), 2.15 (S, 3H), 2.05 (q, 4H), 1.48 (s, 3H), 1.40 (s, 3H), 0.60 (t, 6H).

(2) Preparation of (R)-4-(4-{1-[4-(2-tert-Butylsulfanyl-ethyl)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenoxymethyl)-2,2-dimethyl-[1 ,3]dioxolane

To a stirred solution of (R)-4-(4-{1 -[4-(2-Bromo-ethyl)-3-methyl-phenyl]-1 -ethyl- propyl}-2-methyl-phenoxymethyl)-2,2-dimethyl-[1 ,3]dioxolane (compound prepared in Example 138-(1 )) (1.33 g, 2.72 mmol) in 27.0 ml of acetone were added t-BuSH (0.46 ml, 4.08 mmol) and KOH (275 mg, 4.90 mmol) in 27.0ml of EtOH. The reaction mixture was refluxed for 5.0 h. The mixture was poured into water and the products were extracted with EtOAc. The extracts were washed with brine, dried over Na2SO-1, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane:EtOAc (10:1 ) to give the title compound (962 mg, 71%) as yellowish sticky oil. 1H-NMR (300MHz, CDCI3): 7.05 (m, 1 H), 7.00-6.85 (m, 4H), 6.70 (d, 1 H), 4.50 (m, 1 H), 4.15 (m, 1 H), 4.05 (m, 1 H), 4.00-3.90 (m, 2H), 2.90-2.65 (m, 4H), 2.25 (s, 3H), 2.15 (s, 3H), 2.05 (q, 4H), 1.45 (s, 3H), 1.40 (s, 3H), 1.35 (s, 9H), 0.60 (t, 6H).

(3) Preparation of 4(R)-[4-(1 -Ethyl-1 -{3-methyl-4-[2-(2-methyl-propane-2- sulfinyl)-ethyl]-phenyl}-propyl)-2-methyl-phenoxymethyl]-2,2 -dimethyl- [1 ,3]dioxolane

To a solution of (R)-4-(4-{1-[4-(2-tert-Butylsulfanyl-ethyl)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenoxymethyl)-2,2-dimethyl-[1 ,3]dioxolane (compound prepared in Example 138-(2)) (379 mg, 0.76 mmol) in EtOH/H2O (1/2 v/v, 0.76 ml) at 0 degrees C was added NaIO4 (163 mg, 0.76 mmol) and the mixture was stirred for 5 h. The mixture was poured into water and the products were extracted with CH2CI2. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with CH2CI2:MeOH (30:1 ) to give the title compound (366 mg, 94%) as a white amorphous. 1H-NMR (300MHz, CDCI3): 7.05 (m, 1 H), 7.00-6.85 (m, 4H), 6.70 (d, 1 H), 4.45 (m, 1 H), 4.15 (m, 1 H), 4.05 (m, 1 H), 4.00-3.90 (m, 2H), 3.20 (m, 1 H), 3.00 (m, 1 H), 2.70 (m, 2H), 2.30 (s, 3H), 2.15 (s, 3H), 2.05 (q, 4H), 1.45 (s, 3H), 1.40 (s, 3H), 1.25 (s, 9H), 0.60 (t, 6H) M.S.(ESI+): [M+H]+= 515

(4) Preparation of 3-[4-(1-Ethyl-1-{3-methyl-4-[2-(2-methyl-propane-2-sulfinyl) - ethyl]-phenyl}-propyl)-2-methyl-phenoxy]-propane-1 ,2(S)-diol HO

To a stirred solution of 4(R)-[4-(1-Ethyl-1-{3-methyl-4-[2-(2-methyl-propane-2- sulfinyl)-ethyl]-phenyl}-propyl)-2-methyl-phenoxymethyl]-2,2 -dimethyl- [1 ,3]dioxolane (compound prepared in Example 138-(3)) (366 mg, 0.71 mmol) in THF/H2O (5/1 v/v, 3.2 ml) was added TFA (0.55 ml_, 7.10 mmmol) at 0 degrees C under N2 atmosphere and the reaction mixture was stirred at room temperature for 5.0 h. The mixture was poured into sat. NaHCOs aq. and the products were extracted with CH2CI2. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane:EtOAc (1 :1) to give the title compound (109 mg, 32%) as colorless sticky oil. 1H-NMR (300MHz, CDCI3): 7.05(m, 1 H), 7.00-6.85 (m, 4H), 6.70 (d, 1 H), 4.15 (m, 1H), 4.05 (m, 2H), 3.90-3.70 (m, 2H), 3.20 (m, 1 H), 3.00 (m, 1 H), 2.65 (m, 2H), 2.30 (s, 3H), 2.20 (s, 3H), 2.05 (q, 4H), 1.25 (s, 9H), 0.60 (t, 6H); MS (ESI+) : 475 ([M+H∏.

Example 139 Preparation of 3-[4-(1-Ethyl- 1 -{3-methyl-4-[2-(2-methyl-propane-2-sulfonyl)- ethyl]-phenyl}-propyl)-2-methyl-phenoxy]-propane-1 ,2(S)-diol

HOΥO H0 (1) Preparation of (R)-4-[4-(1-Ethyl-1-{3-methyl-4-[2-(2-methyl-propane-2- sulfonyl)-ethyl]-phenyl}-propyl)-2-methyl-phenoxymethyl]-2,2 -dimethyl- [1 ,3]dioxolane To a stirred solution of (R)-4-(4-{1-[4-(2-tert-Butylsulfanyl-ethyl)-3-methyl- phenyll-i-ethyl^ropylJ^-methyl-phenoxymethyO^^-dimethyl-ti .SJclioxolane (compound prepared in Example 138-(2)) (503 mg, 1.00 mmol) in CH2CI2 (5 ml) was added mCPBA (757 mg, 2.5 mmol) at 0 degrees C and the reaction mixture was stirred for 12 h at room temperature. The mixture was poured into Na2S2O3 aq. and the products were extracted with CH2CI2. The extracts were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane: EtOAc (3:1) to give the title compound (320 mg, 60%) as a white amorphous. 1 H-NMR (300MHz, CDCI3): 7.05 (m, 1 H), 7.00-6.85 (m, 4H), 6.70 (d, 1 H), 4.45 (m, 1 H), 4.15 (m, 1 H), 4.05 (m, 1 H), 4.00-3.90 (m, 2H), 3.20- 3.00 (m, 4H), 2.30 (s, 3H), 2.15 (s, 3H), 2.05 (q, 4H)1 1.50 (s, 3H), 1.48 (s, 9H), 1.40 (s, 3H), 0.60 (t, 6H); MS (ESI+) : 548 ([M+NH4]+).

(2) Preparation of (S)-3-[4-(1 -Ethyl-1 -{3-methyl-4-[2-(2-methyl-propane-2- sulfonyl)-ethyl]-phenyl}-propyl)-2-methyl-phenoxy]-propane-1 ,2-diol

hκ/V"o HO

Using the same procedure as described for the preparation of Example 138-(4), the title compound was prepared from (R)-4-[4-(1-Ethyl-1-{3-methyl-4-[2-(2- methyl-propane-2-sulfonyl)-ethyl]-phenyl}-propyl)-2-methyl-p henoxymethyl]-2,2- dimethyl-[1 ,3]dioxolane (compound prepared in Example 139-(1)). The yield was 56%. 1H-NMR (300MHz, CDCI3): 7.05 (m, 1 H), 7.00-6.85 (m, 4H), 6.70 (d, 1 H), 4.15 (m, 1 H), 4.05 (m, 2H), 3.90-3.70 (m, 2H), 3.20-3.00 (m, 4H), 2.55 (d, 1 H), 2.30 (s, 3H), 2.20 (s, 3H), 2.05 (m, 5H), 1.50 (s, 9H), 0.60 (t, 6H); MS (ESI+) : 508 ([M+NH4]+). Example 140 Preparation of 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt

NaO2Cs OH ' ' OH (1) Preparation of 5(R)-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-meth yl- phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one

H )H O *' To a stirred solution of 4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 19-(2)) (702 mg, 1.83 mmol) in N,N-dirnethylacetamide (18 ml) were added K2CO3 (633 mg, 4.58 mmol) and toluene-4-sulfonic acid (R)-5-oxo-tetrahydro-furan-2-ylmethyl ester (743 mg, 2.75 mmol) and the mixture was stirred at 130 degrees C for 3 h. The reaction mixture was cooled to room temperature and poured into aqueous NH4CI. The products were extracted with ethyl acetate and hexane. The extracts were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (ethyl acetate/hexane = 20/80 to 35/65) to give the title compound (755 mg, 86 %). 1H-NMR: 0.59 (t, 6H), 0.89 (s, 9H), 1.38 (d, 1 H), 1.44-1.55 (m, 1 H), 1.74-1.84 (m, 1 H), 2.03 (q, 4H), 2.15 (s, 3H), 2.25 (s, 3H), 2.27-2.62 (m, 4H), 2.72-2.91 (m, 2H), 3.21-3.27 (m, 1 H), 4.04-4.19 (m, 2H), 4.84-4.91 (m, 1 H), 6.66 (d, 1 H), 6.89- 6.97 (m, 4H), 7.02 (d, 1 H).

(2) 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl} -2- methyl-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt NaO2C OH

To a solution of 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 140-(1 )) (547 mg, 1.14mmol) in methanol (4.5 ml) and tetrahydrofuran (4.5 ml) was added 1 N KOH solution (4.55 ml) and the mixture was stirred for 1 h at room temperature. The reaction mixture was concentrated in vacuo and poured into aqueous KHSO4and the products were extracted with AcOEt. The extracts were washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue (524 mg) was dissolved with MeOH (2 ml) and 1.0M solution of NaOMe in MeOH (1.027 ml, 1.051 mmol) was added. The mixture was stirred for 2 min. and concentrated in vacuo to give the title compound (545 mg, 92%). 1H-NMR (CD3OD): 0.58 (t, 6H), 0.86 (s, 9H), 1.43-1.54 (m, 1 H), 1.73-1.99 (m, 3H), 2.04 (q, 4H), 2.14 (s, 3H), 2.23 (s, 3H), 2.36 (dt, 2H), 2.48-2.58 (m, 1 H), 2.81-2.91 (m, 1H), 3.15 (dd, 1 H), 3.88-3.97 (m, 3H), 6.75 (d, 1 H), 6.83-7.02 (m, 5H); MS (ESI-) : 497 ([M-H]").

Example 141 Preparation of 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt

NaO2C, OH ' 1 OH (1 ) Preparation of 5(R)-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one To a stirred solution of 4-{1-Ethyl-1-[4-(3-hydroxy-4,40-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 20) (670 mg, 1.75 mmol) in N,N-dimethylacetamide (17 ml) were added K2CO3 (605 mg, 4.38 mmol) and toluene-4-sulfonic acid (R)-5-oxo-tetrahydro-furan-2-ylmethyl ester (710 mg, 2.63 mmol) and the mixture was stirred at 130 degrees C for 3 h. The reaction mixture was cooled to room temperature and poured into aqueous NH4CI. The products were extracted with ethyl acetate and hexane. The extracts were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (ethyl acetate/hexane = 20/80 to 35/65) to give the title compound (330 mg, 39%). 1H-NMR: 0.59 (t, 6H), 0.89 (s, 9H), 1.38 (d, 1H), 1.44-1.55 (m, 1H), 1.74-1.84 (m, 1 H), 2.03 (q, 4H), 2.15 (s, 3H), 2.25 (s, 3H), 2.27-2.62 (m, 4H), 2.72-2.91 (m, 2H), 3.21-3.27 (m, 1 H), 4.04-4.19 (m, 2H), 4.84-4.91 (m, 1 H), 6.66 (d, 1H), 6.89- 6.97 (m, 4H), 7.01 (d, 1 H).

(2) 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl} -2- methyl-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt

H NaO H

To a solution of 5-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 141 (1)) (306 mg, 0.636 mmol) in methanol (2.5 ml) and tetrahydrofuran (2.5ml) was added 1 N KOH solution (2.55 ml) and the mixture was stirred for 1 h at room temperature. The reaction mixture was concentrated in vacuo and poured into aqueous KHSO4 and the products were extracted with AcOEt. The extracts were washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue (316 mg) was dissolved with MeOH (2 ml) and 1.0M solution of NaOMe in MeOH (0.621 ml, 0.635 mmol) was added. The mixture was stirred for 2 min. and concentrated in vacuo to give the title compound (330 mg, 100%). 1H-NMR (CD3OD): 0.58 (t, 6H), 0.86 (s, 9H), 1.43-1.54 (m, 1 H), 1.73-1.99 (m, 3H), 2.04 (q, 4H), 2.14 (s, 3H), 2.23 (s, 3H), 2.36 (dt, 2H), 2.48-2.58 (m, 1 H), 2.81-2.91 (m, 1 H), 3.15 (dd, 1 H), 3.88-3.97 (m, 3H), 6.74 (d, 1 H), 6.83-7.02 (m, 5H); MS (ESI-): 497 ([M-HV).

Example 142 Preparation of 5-(2-Chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)- phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt

OH (1 ) Preparation of 5(R)-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl- pentyl)-phenyl]-1-ethyl-propyl}-phenoxymethyl)-dihydro-furan -2-one

Cl Cl OH O' uι uι OH To a stirred solution of 2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pent- 1-ynyl)-phenyl]-1-ethyl-propyl}-phenol (compound prepared in Example 16-(6)) (6 mg, 0.014 mmol) in N,N-dimethylacetamide (0.14 ml) were added K2CO3 (4.9 mg, 0.035 mmol) and toluene-4-sulfonic acid (R)-5-oxo-tetrahydro-furan-2- ylmethyl ester (7.6 mg, 0.028 mmol) and the mixture was stirred at 130 degrees C for 1.5 h. The reaction mixture was cooled to room temperature and poured into aqueous NH4CI. The products were extracted with ethyl acetate and hexane. The extracts were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was purified by preparative TLC (ethyl acetate/hexane = 2/3) to give the title compound (6.0 mg, 81%). 1H-NMR: 0.61 (t, 6H), 0.89 (s, 9H), 1.42-1.59 (m, 2H), 1.81-1.92 (m, 1 H), 2.02 (q, 4H), 2.35-2.75 (m, 4H), 2.90-3.02 (m, 2H), 3.21-3.31 (m, 1 H), 4.07-4.27 (m, 2H), 4.86-4.91 (m, 1 H), 6.79 (d, 1 H), 6.91 (dd, 1 H), 6.98 (dd, 1 H), 7.11-7.19 (m, 3H).

(2) Preparation of 5-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl) - phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt

OH

To a solution of (5R)-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pent yl)- phenyl]-1-ethyl-propyl}-phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 142-(1 )) (6.0 mg, 0.012 mmol) in methanol (0.5 ml) and tetrahydrofuran (0.5ml) was added 1 N KOH solution (0.5 ml) and the mixture was stirred for 1 h at room temperature. The reaction mixture was concentrated in vacuo and poured into aqueous KHSO4 and the products were extracted with AcOEt. The extracts were washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue (6.1 mg) was dissolved with MeOH (0.5 ml) and 1.0M solution of NaOMe in MeOH (0.0111 ml, 0.0114 mmol) was added. The mixture was stirred for 2 min. and concentrated in vacuo to give the title compound (6.2 mg, 96%). 1H-NMR (CD3OD): 0.62 (t, 6H), 0.86 (s, 9H), 1.28-1.98 (m, 4H), 2.06 (q, 4H), 2.37 (t, 2H), 2.64-2.74 (m, 1 H), 2.92-3.01 (m, 1 H), 3.12-3.15 (m, 1 H), 3.97 (s, 3H), 6.96-7.20 (m, 6H); MS (ESI-): 537 ([M-HV).

Example 143 Preparation of 5-(2-Chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)- phenyl]-1-ethyl-propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt OH (1) Preparation of 5(R)-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl- pentyl)-phenyl]-1-ethyl-propyl}-phenoxymethyl)-dihydro-furan -2-one

Cl OH O' uι uι OH To a stirred solution of 2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pent- 1-ynyl)-phenyl]-1-ethyl-propyl}-phenol (compound prepared in Example 17) (6 mg, 0.014 mmol) in N,N-dimethylacetamide (0.14 ml) were added K2CO3 (4.9 mg, 0.035 mmol) and toluene-4-sulfonic acid (R)-5-oxo-tetrahydro-furan-2- ylmethyl ester (7.6 mg, 0.028 mmol) and the mixture was stirred at 130 degrees C for 1.5 h. The reaction mixture was cooled to room temperature and poured into H2O. The products were extracted with ethyl acetate and hexane. The extracts were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was purified by preparative TLC (ethyl acetate/hexane = 2/3) to give the title compound (6.0 mg, 81 %). 1H-NMR: 0.61 (t, 6H), 0.89 (s, 9H), 1.42-1.59 (m, 2H), 1.82-1.91 (m, 1 H), 2.02 (q, 4H), 2.35-2.76 (m, 4H), 2.90-3.02 (m, 2H), 3.21-3.30 (m, 1 H), 4.07-4.27 (m, 2H), 4.86-4.91 (m, 1 H), 6.80 (d, 1 H), 6.91 (dd, 1 H), 6.98 (dd, 1 H), 7.11-7.17 (m, 3H).

(2) 5-(2-Chloro-4-{1 -[3-chloro-4-(3-hydroxy-4,4-dimethyl-pentyl)-phenyl]-1 -ethyl- propyl}-phenoxy)-4(R)-hydroxy-pentanoic acid sodium salt

NaO"11 — Y^O OH

To a solution of (5R)-(2-Chloro-4-{1-[3-chloro-4-(3-hydroxy-4,4-dimethyl-pent yl)- phenyl]-1-ethyl-propyl}-phenoxymethyl)-dihydro-furan-2-one(c ompound prepared in Example 143-(1 )) (6.0 mg, 0.012 mmol) in methanol (0.5 ml) and tetrahydrofuran (0.5ml) was added 1 N KOH solution (0.5 ml) and the mixture was stirred for 1 h at room temperature. The reaction mixture was concentrated in vacuo and poured into aqueous KHSO4 and the products were extracted with AcOEt. The extracts were washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue (6.3 mg) was dissolved with MeOH (0.5 ml) and 1.0M solution of NaOMe in MeOH (0.0114 ml, 0.0117mmol) was added. The mixture was stirred for 2 min. and concentrated in vacuo to give the title compound (6.6 mg, 96%). 1H-NMR (CD3OD): 0.62 (t, 6H), 0.86 (s, 9H), 1.28-2.01 (m, 4H), 2.06 (q, 4H), 2.37 (t, 2H), 2.63-2.74 (m, 1H), 2.92-3.01 (m, 1H), 3.13 (dd, 1H), 3.97 (s, 3H), 6.96-7.20 (m, 6H); MS (ESI-) : 537 ([M-H]").

Example 144 Preparation of (R)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-pyrrolidin-2- one

AY^-o

Preparation of (R)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-pyrrolidin-2- one

To a solution of 4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(5)) (300 mg, 0.788 mmol) in MeCN (5 ml), toluene-4-sulfonic acid (R)-5-oxo-pyrrolidin-2- ylmethyl ester (425 mg, 1.577 mmol) and K2CO3 (545 mg, 3.942 mmol) were added at room temperature and the mixture was stirred at 108 degrees C for 24 h. To the mixture, ethyl acetate was added and the mixture was washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:EtOAc= 100:0 to 0:100) to give the title compound (159.2 mg, 42.3%). 1H-NMR (CDCI3): 0.61 (t, 6H, J=I.2Hz), 0.92 (t, 6H, J=7.5Hz), 1.64-1.60 (q, 4H1 J=7.5Hz), 1.86-2.00 (m, 1 H), 2.05 (q, 4H, J=7.2Hz), 2.15 (s, 3H), 2.31 (s, 3H), 4.07-4.13 (m, 3H), 3.31 (dd, 2H, J=7.5, 9.3Hz), 3.97 (dd, 1 H, J=3.8, 9.3Hz), 4.07-4.13 (m, 1 H), 6.01 (d, 1 H, J=15.9Hz), 6.64 (d, 1 H, J=8.4Hz), 6.74 (d, 1 H, J=15.9Hz), 6.90-6.96 (m, 4H), 7.29 (d, 1 H, J=8.7Hz); MS (ESI+) : 478 ([M+H]+).

Example 145 Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-pyrrolidin-2- one

o

Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-pyrrolidin-2- one

To a solution of 4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(5)) (300 mg, 0.788 mmol) in MeCN (5 ml), toluene-4-sulfonic acid (S)-5-oxo-pyrrolidin-2- ylmethyl ester (425 mg, 1.577 mmol) and K2CO3 (545 mg, 3.942 mmol) were added at room temperature and the mixture was stirred at 108 degrees C for 24 h. To the mixture, ethyl acetate was added and the mixture was washed with brine, dried over magnesium sulfate, concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane: EtOAc= 100:0 to 0:100) to give the title compound (152.6 mg, 40.5%). 1H-NMR (chloroform-d): 0.61 (t, 6H, J=7.2Hz), 0.92 (t, 6H, J=7.5Hz), 1.64 (q, 4H, J=7.5Hz), 1.67 (s, 1 H), 1.88-1.99 (m, 1 H), 2.05 (q, 4H, J=7.2Hz), 2.15 (s, 3H), 2.31 (S1 3H), 2.27-2.52 (m, 2H), 3.81 (dd, 1H1 J=7.5, 9.3Hz), 3.97 (dd, 1 H, J=3.8, 9.3Hz), 4.06-4.13 (m, 1 H), 5.99 (brs, 1 H), 6.01 (d, 1 H, J=15.9Hz), 6.64 (d, 1 H, J=8.1 Hz), 6.74 (d, 1 H), 6.89-6.98 (m, 4H), 7.29 (d, 1 H); MS (ESI+) : 478 ([M+H]+).

Example 146 Preparation of 3-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-benzoic acid

COOH Preparation of 3-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-benzoic acid

COOH To a solution of compound prepared in Example 1-(5) (4-{1 -Ethyl-1 -[4-(3-ethyl- 3-hydroxy-(1 E)-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol ) (20 mg, 0.0526 mmol) in DMF (0.4 ml), K2CO3 (21.8 mg, 0.158 mmol ) and 3- bromomethyl-benzoic acid methyl ester (14.5 mg, 0.0632 mmol) were added at room temperature and the mixture was stirred at 120 degrees C for 16 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O and brine, dried over MgSO4, concentrated in vacuo. The obtained residue was dissolved in MeOH (0.5 ml), and 1N NaOH (0.2 ml) was added at room temperature and the mixture was stirred at 45 degrees C for 11 h. The mixture was evaporated in vacuo and the obtained residue was chromatographed on silica gel (n-hexane: EtOAc= 100:0 to 0:100) and re-purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (4.7 mg, 17%). 1H-NMR: 0.62 (t, 6H), 0.92 (t, 6H), 1.62 (q, 4H), 2.03 (q, 4H), 2.20 (s, 3H), 2.34 (S1 3H), 5.06 (S, 2H), 6.01 (d, 1 H), 6.68 (d, 1 H), 6.78 (s, 1 H), 7.50 (t, 1 H), 7.68 (d, 1 H), 8.02 (d, 1 H), 8.12 (s, 1 H); MS (ESI+) : 532 ([M+NH4]+).

Example 147 Preparation of 4-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-benzoic acid

HOOC (1 ) Preparation of 4-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-benzoic acid methyl ester

MeOOC^^ To a solution of compound prepared in Example 1-(5) (20 mg, 0.0526 mmol) (4- {1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-(1 E)-pent-1 -enyl)-3-methyl-phenyl]-propyl}-2- methyl-phenol ) in DMF (0.5 ml), K2CO3 (29 mg, 0.21 mmol ) and 4- bromomethyl-benzoic acid methyl ester (14.4 mg, 0.0631 mmol) were added at room temperature and the mixture was stirred for 16 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was purified by prerparative TLC (ethyl acetate/hexane = 1/1) to give the title compound (25.3 mg. 91 %). 1H-NMR: 0.61 (t, 6H), 0.92 (t, 6H)1 1.64 (q, 4H), 2.03 (q, 4H), 2.24 (s, 3H), 2.31 (s, 3H), 3.93 (s, 3H), 5.09 (s, 2H), 6.00 (d, 1 H), 6.71-6.77 (m, 2H), 6.92-6.95 (m, 4H), 7.50 (d, 2H), 8.04 (d, 2H); MS (ESI+) : 511 ([M-OH]+). (2) Preparation of 3-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-benzoic acid

MeOOC HOOC To a solution of 4-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-benzoic acid methyl ester (compound prepared in Example 147-(1 )) (25.3 mg, 0.0479 mmol) in EtOH (2 ml), 1 N NaOH (0.1 ml) was added at room temperature, and the mixture was stirred at 40 degrees C for 16h and concentrated in vacuo. The obtained residue was purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (19.0 mg, 77%). 1H-NMR: 0.61 (t, 6H), 0.92 (t, 6H), 1.66 (q, 4H), 2.05 (q, 4H), 2.05 (s, 3H), 2.31 (s, 3H), 5.12 (s, 2H), 6.00 (d, 1 H), 6.70-6.80 (m, 2H), 7.54 (d, 2H), 8.11 (d, 2H); MS (ESI+) : 497([M-OH]+).

Example 148 Preparation of (E)-3-Ethyl-1 -(4-{1 -ethyl-1 -[3-methyl-4-(pyridin-3-ylmethoxy)- phenyl]-propyl}-2-methyl-phenyl)-pent-1-en-3-ol

Preparation of (E)-3-Ethyl-1 -(4-{1 -ethyl-1 -[3-methyl-4-(pyridin-3-ylmethoxy)- phenyl]-propyl}-2-methyl-phenyl)-pent-1-en-3-ol To a solution of compound prepared in Example 1-(5) (4-{1 -Ethyl-1 -[4-(3-ethyl- 3-hydroxy-(1 E)-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol) (20 mg, 0.0526 mmol) in DMF (0.5 ml), K2CO3 (60 mg, 0.435 mmol) and 3-bromomethyl- pyridine hydrochloride (25.0 mg, 0.099 mmol) were added and the mixture was stirred at 110 degrees C for 80 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O and brine, dried over MgSO4, concentrated in vacuo. The obtained residue was purified by prerparative TLC (ethyl acetate:hexane = 1 :3) to give the title compound (11.7 mg, 47%). 1H-NMR: 0.61 (t, 6H), 0.92 (t, 6H), 1.63 (q, 4H), 2.04 (q, 4H), 2.22 (s, 3H), 2.32 (s, 3H), 5.06 (s, 2H), 6.01 (d, 1H), 6.72-6.88 (m, 2H), 7.24-7.37 (m, 3H), 7.80 (d, 1 H), 8.57 (d, 1 H), 8.60 (s, 1 H); MS (ESI+) : 454 ([M-OH]+).

Example 149 Preparation of (E)-3-Ethyl-1 -(4-{1 -ethyl-1 -[3-methyl-4-(pyridin-4-ylmethoxy)- phenyl]-propyl}-2-methyl-phenyl)-pent-1-en-3-ol

Preparation of (E)-3-Ethyl-1-(4-{1 -ethyl-1 -[3-methyl-4-(pyridin-4-ylmethoxy)- phenyl]-propyl}-2-methyl-phenyl)-pent-1-en-3-ol

To a solution of compound prepared in Example 1-(5) (4-{1 -Ethyl-1 -[4-(3-ethyl- 3-hydroxy-(1 E)-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol ) (20 mg, 0.0526 mmol) in DMF (0.5 ml), K2CO3 (29 mg, 0.210 mmol) and 4-chloromethyl- pyridine hydrochloride (10.3 mg, 0.063 mmol) were added and the mixture was stirred at room temperature for 16 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O and brine, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was purified by prerparative TLC (ethyl acetate: hexane = 1 :3) to give the title compound (17.8 mg, 72%). 1H-NMR: 0.61 (t, 6H), 0.92 (t, 6H)1 1.64 (q, 4H), 2.05 (q, 4H), 2.26 (s, 3H), 2.31 (s, 3H), 5.06 (s, 2H)1 6.01 (d, 1 H), 6.70-6.80 (m, 2H), 6.92-6.97 (m, 4H) , 7.25 (d, 1 H), 7.38 (d, 2H), 8.62 (d, 2H); MS (ESI+) : 454 ([M-OH]+).

Example 150 Preparation of 4-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-benzoic acid methyl ester

HOOC

(1) Preparation of 4-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]-propyl}-2- methyl-phenoxy)-benzoic acid methyl ester

To a solution of compound prepared in Example 1-(5) (4-{1 -Ethyl-1 -[4-(3-ethyl- 3-hydroxy-(1 E)-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol) (20 mg, 0.0526 mmol) in DMF (0.5 ml), K2CO3 (21.8 mg, 0.158 mmol ) and 4-fluoro- benzoic acid methyl ester (13.3 mg, 0.0789 mmol) were added and the mixture was stirred at 110 degrees C for 16 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O and brine, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was purified by prerparative TLC (ethyl acetate:hexane = 1 :3) to give the title compound (19.0 mg, 70%). 1H-NMR: 0.64 (t, 6H), 0.92 (t, 6H), 1.62 (q, 4H), 2.05-2.11 (m, 7H), 2.33 (s, 3H), 3.88 (s, 3H), 6.02 (d, 1H), 6.73-7.34 (m, 9H), 7.96 (d, 2H); MS (ESI+) : 515 ([M+H]+). (2) Preparation of 4-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-benzoic acid

MeOOC HOOC

To a solution of 4-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-met hyl- phenyl]-propyl}-2-methyl-phenoxy)-benzoic acid methyl ester (compound prepared in Example 150-(1)) (17 mg, 0.0331 mmol) in EtOH (2 ml), 1 N NaOH (0.1 ml) was added, and the mixture was stirred at 50 degrees C for 16h and concentrated in vacuo. The obtained residue was purified by preparative TLC (CHCl3:MeOH=8:3 saturated with H2O and ethyl acetate:hexane = 1 :1 saturated with H2O) to give the title compound (3.2 mg, 19 %). 1H-NMR: 0.65 (t, 6H), 0.93 (t, 6H), 1.66 (q, 4H), 2.05-2.34 (m, 7H), 2.34 (s, 3H), 6.03 (d, 1 H), 6.73-7.35 (m, 9H), 8.02 (d, 2H); MS (ESI+) : 518 ([M+NH4]+).

Example 151 Preparation of (E)-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-acetic acid

HOoC^O

(1 ) Preparation of (E)-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3-methy l- phenyl]-propyl}-2-methyl-phenoxy)-acetic acid methyl ester

MeO9C^O

To a stirred solution of 4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(5)) (700 mg, 1.84 mmol) in acetone (18 ml) were added K2CO3 (763 mg, 5.52 mmol) and bromoaceticacid methyl ester (563 mg, 3.68 mmol) at room temperature and the mixture was refluxed for 4 h. The reaction mixture was concentrated and poured into H2O and the products were extracted with ethyl acetate. The extracts were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (ethyl acetate/hexane = 0/100 to 5/95) to give the title compound (892 mg, quant). 1H-NMR: 0.61 (t, 6H), 0.92 (t, 6H), 1.64 (q, 4H), 2.05 (q, 4H), 2.23 (s, 3H), 2.31(s, 3H), 3.80 (s, 3H)1 4.62 (s, 2H), 6.02 (d, 1 H), 6.57 (d, 1 H), 6.75 (d, 1 H), 6.92-6.94 (m, 4H) 7.30 (d, 1H).

(2) Preparation of (E)-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3-methy l- phenyl]-propyl}-2-methyl-phenoxy)-acetic acid

MeO9C^O' 1^OH HO2C v I Γ*QH

To a solution of (4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-acetic acid methyl ester (compound prepared in Example 151-(1)) (892 mg, 1.97 mmol) in methanol (3 ml) and tetrahydrofuran (2 ml) was added 1 N KOH solution (3 ml) and the mixture was stirred for 2 h at room temperature. The reaction mixture was poured into aqueous KHSO4, and the products were extracted with AcOEt. The extracts were washed with brine, dried over MgSO4, filtered and concentrated in vacuo to give the title compound (807 mg, 100 %). 1H-NMR: 0.60 (t, 6H), 0.92 (t, 6H), 1.64 (q, 4H), 2.05 (q, 4H), 2.23 (s, 3H), 2.31 (s, 3H), 4.65 (s, 2H), 6.01 (d, 1H), 6.62 (d, 1 H), 6.75 (d, 1 H), 6.92-6.97 (m, 4H) 7.29 (d, 1 H).

Example 152 Preparation of (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4-diol OH

Preparation of (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-methoxymethoxy- 3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-pheno xy)-pentane-1 ,4-diol

To a solution of (R)-5-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 46-(1 )) (39 mg, 0.065 mmol) in Et2O (1 ml), LAH (7 mg, 0.195 mmol) was added and the mixture was stirred at room temperature for 18 h. To the mixture, ethyl acetate and brine were added and the organic layer was filtered through celite, and the filtrate was concentrated in vacuo. To the solution of the residue (7.3 mg) in i- PrOH (0.1 ml), CBr4 (0.33 mg 0.001 mmol) was added and the mixture was stirred at 85 degrees C for 3.5 h. The mixture was purified by silica gel chromatography (n-hexane/ethyl acetate =1/1 ) to give the title compound (7.2 mg, 91.7%). 1H-NMR (chloroform-d): 0.59 (t, 6H, J=7.2Hz), 1.67-1.83 (m, 4H), 2.04 (q, 4H, J=7.2Hz), 2.14 (s, 3H), 2.37 (s, 3H), 2.83 (brs, 1 H), 3.66-3.77 (m, 2H), 3.81 (dd, 1 H, J=7.4, 9.2Hz), 3.92 (dd, 1 H, J=3.5, 9.2Hz), 3.86-4.09 (m, 1 H), 4.72 (brs, 1 H), 6.65 (d, 1 H, J=8.6Hz), 6.83-7.04 (m, 5H), 7.33 (d, 1 H, J=-8.0Hz); MS(ESI+) : 583([M+Na]+).

Example 153 Preparation of (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1 -ynyl)-phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol Preparation of (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4-cliol

CF?H To a solution of (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-propyl} -2-nnethyl- phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 2-(3)) (38 mg, 0.063 mmol) in Et2O (1 ml), LAH (7.2mg 0.19mmol) was added and the mixture was stirred at room temperature for 18 h. To the mixture, ethyl acetate and brine were added and the organic layer was filtered through celite, and the filtrate was concentrated in vacuo. To the solution of the residue (7.3 mg) in i- PrOH (0.1 ml), CBr4 (0.33 mg 0.001 mmol) was added and the mixture was stirred at 85 degrees C for 3.5 h. The mixture was purified by silica gel chromatography (n-hexane/ethyl acetate =1/1) to give the title compound (5 mg, 74.4%). 1H-NMR (chloroform-d): 0.59 (t, 6H, J=7.3Hz), 1.53-1.80 (m, 4H), 2.05 (q, 4H, J=7.3Hz), 2.15 (s, 3H), 2.37 (s, 3H), 2.80 (brs, 1 H), 3.73 (dd, 2H, J=5.0, 10.7Hz), 3.82 (dd, 1 H, J=7.4, 9.3Hz), 3.93 (dd, 1H, J=3.6, 9.3Hz), 4.01-4.10 (m, 1H), 4.31 (brs, 1H), 6.66 (d, 1H, J=8.5Hz), 6.83-7.04 (m, 4H), 7.34 (d, 1H, J=8.1Hz); MS (ESI+): 583 ([M+Na]+).

Example 154 Preparation of (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4-diol 07747

368

OH

Example 155 Preparation of (E)-4-[4-(1 -Ethyl- 1 -{3-methyl-4-[(R)-1 -(tetrahydro-furan-2- yl)methoxy]-phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but- 3-en-2-ol

Preparation of (R)-5-(4-{1 -Ethyl-1-[S-methyl^-CCEH^^-trifluoro-S-hydroxy-S- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4-diol and (E)-4-[4-(1 -Ethyl-1-{3-methyl-4-[(R)-1-(tetrahydro-furan-2-yl)methoxy]- phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1-trifluoro-2-trifluoromethyl-but-3-en-2-ol

Example 155 To a solution of (R)-5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 48-(1 )) (39.9 mg, 0.066 mmol) in Et2O (1 ml), LAH (7.5 mg, 0.199 mmol) was added and the mixture was stirred at room temperature for 18 h. To the mixture, ethyl acetate and brine were added and the organic layer was filtered through celite, and the filtrate was concentrated in vacuo. To the residue (25.6 mg), conc.HCI in MeOH (1 ml) was added and the mixture was stirred at 85 degrees C for 3.5 h. The mixture was chromatographed on silica gel (n-hexane/ethyl acetate =1/1 ) to give the title compounds (example 154 (15 mg, 63.2%) and example 155 (3.5 mg, 15.2%)). Example 154 1H-NMR (chloroform-d): 0.61 (t, 6H, J=7.2Hz), 1.58-1.83 (m, 4H), 2.06 (q, 4H, J=7.2Hz), 2.17 (s, 3H), 2.33 (s, 3H), 2.61 (brs, 1 H), 3.72 (dd, 2H, J=SA 1 10.5Hz), 3.84 (dd, 1H, J=7.2, 9.3Hz), 3.95 (dd, 1 H, J=3.5, 9.3Hz), 3.93 (brs, 1H), 4.01- 4.11 (m, 1 H), 6.08 (d, 1 H, J=15.9Hz), 6.68 (d, 1 H, J=8.4Hz), 6.87-7.06 (m, 4H), 7.33 (d, 1H, J=5.7Hz), 7.37 (d, 1H, J=13.2Hz); MS (ESI+) : 585 ([M+Na∏. Example 155 1H-NMR (chloroform-d): 0.60 (t, 6H, J=7.2Hz), 1.80-2.12 (m, 4H), 2.05 (q, 4H, J=7.2Hz), 2.17 (s, 3H), 2.33 (s, 3H), 3.19 (brs, 1 H), 3.79-4.00 (m, 4H), 4.24-4.33 (m, 1 H), 6.08 (d, 1 H, J=16.2Hz), 6.68 (d, 1 H, J=8.7Hz), 6.87-7.02 (m, 4H), 7.33 (d, 1 H, J=5.1Hz), 7.37 (d, 1 H, J=12.9Hz); MS (ESI+) : 562 ([M+NH4∏.

Example 156 Preparation of (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4-diol

OH Example 157 Preparation of (E)-4-[4-(1 -Ethyl-1-{3-methyl-4-[(S)-1-(tetrahydro-furan-2- yl)methoxy]-phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1 -trifluoro-2-trifluoromethyl-but- 3-en-2-ol Preparation of (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-pentane-1 ,4-diol and (E)-4-[4-(1-Ethyl- 1 -{3-methyl-4-[(S)-1 -(tetrahydro-furan-2-yl)methoxy]- phenyl}-propyl)-2-methyl-phenyl]-1 ,1 ,1 -trifluoro-2-trifluoromethyl-but-3-en-2-ol

O'

Example 157 To a solution of (S)-5-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluorom8thyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 30-(2)) (40.1 mg, 0.067 mmol) in Et2O (1 ml), LAH (7.6 mg, 0.200 mmol) was added and stirred at room temperature for 18 h. To the mixture, ethyl acetate and brine were added and the organic layer was filtered through celite, and the filtrate was concentrated in vacuo. To the residue (20.7 mg), conc.HCI in MeOH (1 ml) was added and the mixture was stirred at 85 degrees C for 3.5 h. To the same residue (13.4 mg) in iPrOH (0.2 ml), CBr4 (0.7 mg, 0.002 mmol) was added and the mixture was stirred at 85 degrees C for 3.5 h. The mixture was chromatographed on silica gel (n-hexane/ethyl acetate =1/1 ) to give the title compounds (example 156 (21.8 mg, 68.9%) and example 157 (1 mg, 5.4%)). Example 156 1H-NMR (chloroform-d): 0.61 (t, 6H, J=7.3Hz), 1.61-1.83 (m, 4H), 2.06 (q, 4H, J=7.3Hz), 2.17 (s, 3H), 2.33 (s, 3H), 2.54 (brs, 1 H), 2.89 (brs, 1 H), 3.77-3.67 (m, 2H), 3.84 (dd, 1 H, J=7.4, 9.3Hz), 0.00 (dd, 1 H, J=3.6, 9.3Hz), 4.01-4.09 (m, 1 H), 4.25 (brs, 1 H), 6.08 (d, 1 H, J=15.8Hz), 6.68 (d, 1 H, J=8.5Hz), 6.89-7.01 (m, 4H)1 7.37 (d, 1 H, J=15.8Hz), 7.34 (d, 1H, J=7.9Hz); MS (ESI+) : 585([M+Na]+). Example 157 1H-NMR (chloroform-d): 0.61 (t, 6H), 1.83-2.16 (m, 4H), 2.05 (q, 4H, J=7.3Hz), 2.17 (s, 3H), 2.33 (s, 3H), 3.20 (brs, 1H), 3.79-4.01 (m, 4H), 4.25-4.33 (m, 1H), 6.08 (d, 1 H1 J=15.3Hz), 6.68 (d, 1 H, J=8.7Hz), 6.87-6.97 (m, 2H), 6.99-7.03 (m, 2H), 7.33 (d, 1H, J=7.8Hz), 7.36 (d, 1H, J=15.3Hz); MS (ESI+): 567([M+Na]+).

Example 158 Preparation of (R)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol

OH Preparation of (R)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol

fY^o

To a solution of (R)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one (compound prepared in Example 44) (55.7 mg, 0.116 mmol) in Et2O (3 ml), LAH (13 mg, 0.349 mmol) was added and the mixture was stirred at room temperature for 18 h. To the mixture, ethyl acetate and brine were added and the organic layer was filtered through celite, and the filtrate was concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane/ethyl acetate =1/3 to ethyl acetate) to give the title compound (18.7 mg, 33.3%). 1H-NMR (chloroform-d): 0.61 (t, 6H, J=7.4Hz), 0.92 (t, 6H, J=7.8Hz), 0.00 (q, 4H, J=7.8Hz), 1.70-1.81 (m, 4H), 2.05 (q, 4H, J=7.4Hz), 2.18 (s, 3H), 2.31 (s, 3H), 2.81 (brs, 1 H), 3.65 (brs, 1 H), 3.68-3.78 (m, 2H), 3.83 (dd, 1 H, J=7.4, 9.3Hz), 3.95 (dd, 1H, J=3.6, 9.3Hz), 4.02-4.11 (m, 1H), 6.01 (d, 1 H, J=15.9Hz), 6.68 (d, 1 H1 J=8.4Hz), 6.74 (d, 1 H1 J=15.9Hz), 6.91-6.97 (m, 4H), 7.30 (d, 1 H, J=8.7Hz); MS (ESI+) : 500 ([M+NH4]+).

Example 159 Preparation of (E)-3-Ethyl-1 -[4-(1 -ethyl-1 -{3-methyl-4-[(R)-1 -(tetrahydro-furan-2- yl)methoxy]-phenyl}-propyl)-2-methyl-phenyl]-pent-1-en-3-ol

Preparation of (E)-3-Ethyl-1 -[4-(1 -ethyl-1 -{3-methyl-4-[(R)-1 -(tetrahydro-furan-2- yl)methoxy]-phenyl}-propyl)-2-methyl-phenyl]-pent-1-en-3-ol

OH To a solution of (R)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol (compound prepared in Example 158) (30 rng, 0.062 mmol) in THF (0.5 ml), PPh3 (48.91 mg, 0.186 mmol), phthalimide (27.43 mg, 0.186 mmol), DEAD (32.47 mg, 0.186 mmol) were added and the mixture was stirred at room temperature for 4 h. The mixture was concentrated in vacuo, and the obtained residue was purified by preparative TLC (n-hexane/ethyl acetate =3/1 and 1/1) to give the title compound (22.1 mg, 76.5%). 1H-NMR (chloroform-d): 0.58 (t, 6H, J=7.5Hz), 0.92 (t, 6H, J=7.2Hz), 1.64 (q, 4H, J=7.2Hz), 1.80-2.15 (m, 4H), 2.05 (q, 4H, J=7.5Hz), 2.18 (s, 3H), 2.31 (s, 3H), 3.79-4.02 (m, 4H), 4.24-4.34 (m, 1 H), 6.01 (d, 1 H1 J=15.9Hz), 6.68 (d, 1 H, J=8.7Hz), 6.75 (d, 1 H, J=16.2Hz), 6.87-6.98 (m, 4H), 7.29 (d, 1 H, J=8.7Hz); MS (ESI+) : 482 ([M+NH4∏. Example 160 Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol

OH Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol

To a solution of (S)-5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3 - methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one (compound prepared in Example 1-(6)) (59.2 mg, 0.124 mmol) in Et2θ (3 ml), LAH (14 mg, 0.371 mmol) was added and the mixture was stirred at room temperature for 18 h. To the mixture, ethyl acetate and brine were added and the organic layer was filtered through celite, and the filtrate was concentrated in vacuo The obtained residue was purified by preparative TLC (n-hexane/ethyl acetate =1/1 and 1/3) to give the title compound (28.8 mg, 48.2%). 1H-NMR (chloroform-d): 0.61 (t, 6H, J=7.3Hz), 0.92 (t, 6H, J=7.6Hz), 1.47 (brs, 1H), 1.64 (q, 4H, J=7.6Hz), 1.72-1.82 (m, 4H), 2.05 (q, 4H, J=7.3Hz), 2.18 (s, 3H), 2.31 (s, 3H), 2.81 (brs, 1 H)1 3.70-3.75 (m, 2H), 3.85 (dd, 1 H, J=7.5, 9.2Hz), 3.95 (dd, 1 H, J=3.5, 9.2Hz), 4.02-4.09 (m, 1 H), 6.01 (d, 1 H, J=16.0Hz), 6.68 (d, 1 H, J=8.3Hz), 6.74 (d, 1 H, J=16.0Hz), 6.90-6.97 (m, 4H), 7.30 (d, 1 H, J=8.8Hz); MS (ESI+) : 500 ([M+NH4f).

Example 161 Preparation of 4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,5,5,5-pentafluoro-3-hydroxy-3- pentafluoroethyl-pent-1-enyl)-phenyl]-propyl}-2-methyl-pheno l (1 ) Preparation of (E)-3-{4-[1 -Ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenylj-acrylic acid methyl ester

OTf COOMe

To a solution of compound prepared in Example 1-(1 ) (trifluoro-methanesulfonic acid 4-[1 -ethyl-1-(4-hydroxy-3-methyl-phenyl)-propyl]-2-methyl-phenyl ester), (200 mg, 0.481 mmol) in DMF (2 ml), NaHCO3 (162 mg, 1.926 mmol), LiBr (29.3 mg, 0.337 mmol), dppp (20 mg, 0.048 mmol), PdCI2(PPh3)2 (33.7 mg, 0.048 mmol) and acrylic acid methyl ester (0.347 ml, 3.85 mmol) were added at room temperature and the mixture was stirred at 140 degrees C for 16h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=100:0 to 50:50) to give the title compound (15 mg, 9%). 1H-NMR: 0.61 (t, 6H), 2.03 (q, 4H), 2.20 (s, 3H), 2.39 (s, 3H), 3.80 (s, 3H)1 4.67 (s, 1 H), 6.32 (d, 1 H), 6.66 (d, 1 H), 7.42 (d ,1 H), 7.96 (d, 1 H).

(2) Preparation of 4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,5,5,5-pentafluoro-3-hydroxy- 3-pentafluoroethyl-pent-1-enyl)-phenyl]-propyl}-2-methyl-phe nol

COOMe X2F5 Hn'

To a solution of C2F5I (0.426 mmol) in diethyl ether (0.5 ml) at -78 degrees C, 1.5M MeLi in diethyl ether (0.284 ml, 0.426 mmol) was added, and then (E)-3-{4- [1 -Ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2-methyl-phenyl}-acryli c acid methyl ester (compound prepared in Example 161-(1)) (15 mg, 0.0426 mmol) in diethyl ether (0.5 ml) were added. The mixture was stirred at -78 degrees C for 10min. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=100:0 to 50:50) to give the title compound (5 mg, 21 %). 1H-NMR: 0.61 (t, 6H), 2.03 (q, 4H), 2.20 (s, 3H), 2.30 (s, 3H), 3.35 (s, 1 H), 5.98 (d, 1 H), 6.66 (d, 1 H), 6.82-6.90 (m, 2H), 6.95-7.00 (m, 2H), 7.35 (d, 1 H); MS (ESI+) : 561 ([M+H]+).

Example 162 Preparation of (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,5,5,5-pentafluoro-3- hydroxy-3-pentafluoroethyl-pent-1-enyl)-phenyl]-propyl}-2-me thyl- phenoxymethyl)-dihydro-furan-2-one

Preparation of (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,5,5,5-pentafluoro-3- hydroxy-3-pentafluoroethyl-pent-1-enyl)-phenyl]-propyl}-2-me thyl- phenoxymethyl)-dihydro-furan-2-one

To a solution of compound prepared in Example 161-(2) (4-{1 -ethyl-1 -[3-methyl- 4-((E)-4,4,5,5,5-pentafluoro-3-hydroxy-3-pentafluoroethyl-pe nt-1-enyl)-phenyl]- propyl}-2-methyl-phenol) (34 mg, 0.0607 mmol) in DMF (0.5 ml), K2CO3 (25.3 mg, 0.183 mmol) and (S)-(+)-dihydro-5-(p-tolenesulfonylmethyl)-2(3H)-furanone (18 mg, 0.0668 mmol) were added at room temperature and stirred at 100 degrees C for 16h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=2:1) to give the title compound (13.7 mg, 34%). 1H-NMR: 0.61 (t, 6H), 2.05 (q, 4H), 2.20 (s, 3H), 2.34 (s, 3H), 2.55-2.63 (m, 2H), 3.90-3.98 (m, 1 H), 4.17-4.22 (m, 1 H), 4.63-4.73 (m ,1 H), 5.89 (d, 1 H), 6.65 (d, 1 H), 6.82-6.90 (m, 2H), 6.97-7.02 (m, 2H), 7.35 (d, 1 H); MS (ESI+): 676 ([M+NH4]+).

Example 163 Preparation of (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,5,5,5-pentafluoro-3- hydroxy-3-pentafluoroethyl-pent-1-enyl)-phenyl]-propyl}-2-me thyl-phenoxy)-4- hydroxy-pentanoic acid

HOOC X2F5 c£H Preparation of (S)-5-(4-{1 -Ethyl-1-[3-methyl-4-((E)-4,4,5,5,5-pentafluoro-3- hydroxy-3-pentafluoroethyl-pent-1-enyl)-phenyl]-propyl}-2-me thyl-phenoxy)-4- hydroxy-pentanoic acid

To a solution of compound prepared in Example 162 ((S)-5-(4-{1-Ethyl-1-[3- methyl-4-((E)-4,4,5,5,5-pentafluoro-3-hydroxy-3-pentafluoroe thyl-pent-1-enyl)- phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one) (8.1 mg, 0.0123 mmol) in MeOH (1 ml), 1 N NaOH (0.1 ml) were added and the mixture was stirred at room temperature for 1 h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (4.4 mg, 54%). 1H-NMR: 0.61 (t, 6H), 2.04 (q, 4H), 2.20 (s, 3H), 2.30 (s, 3H), 2.59 (t, 2H), 3.83- 3.98 (m, 3H), 5.92 (d,1H), 6.66 (d, 1H), 6.83-6.89 (m, 2H), 6.97-7.02 (m, 2H); MS (ESI+): 694 ([M+NH4]+).

Example 164 Preparation of 4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-phenol

(1 ) Preparation of 3-(4-Bromo-3-methyl-phenyl)-pentan-3-ol

COOMe

To a solution of 4-bromo-3-methyl-benzoic acid methyl ester (3.0 g, 13.1 mmol) in THF (300 ml), 0.89M EtMgBr in THF (39.2 ml, 34.9 mmol) were added at 0 degrees C for 5min and stirred at room temperature for 16h. To the mixture, saturated NH4CI solution and ethyl acetate was added and the organic layer was washed with saturated NH4CI solution, dried over MgSO4, concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane only to ethyl acetate/n-hexane = 1/4) to give the title compound (2.71 g, 81 %). 1H-NMR: 0.75 (t, 6H), 1.74-1.82 (m, 4H), 2.40 (s, 3H), 7.00 (dd, 1 H), 7.45 (d, 1 H); MS (ESI+) : 239 ([M-OH]+).

(2) Preparation of 4-[1-(4-Bromo-3-methyl-phenyl)-1-ethyl-propyl]-phenol To a mixture of 3-(4-bromo-3-methyl-phenyl)-pentan-3-ol (150 mg, 0.586 mmol) and phenol (82 mg, 0.88 mmol), trifluoromethanesulfonic acid (0.1 ml) were added at room temperature and the mixture was stirred at room temperature for 16h. The mixture applied onto silica and chromatographed (n-hexane to ethyl acetate/n- hexane = 1/1 ) to give the title compound as mixture of phenol. 1H-NMR: 0.60 (t, 6H)1 2.03 (q, 4H), 2.32 (s, 3H), 6.72 (s, 1H), 6.83-7.38 (m, 6H); MS (ESI+) : 333 ([M+H]+).

(3) Preparation of (E)-1-{4-[1-Ethyl-1-(4-hydroxy-phenyl)-propyl]-2-methyl- phenyl}-pent-1 -en-3-

one To a solution of 4-[1-(4-Bromo-3-methyl-phenyl)-1-ethyl-propyl]-phenol prepared in Example 164-(2) in DMF (3 ml), NaHCO3 (454 mg, 5.4 mmol), LiBr (40 mg, 0.46 mmol), dppp (58 mg, 0.14 mmol), PdCI2(PPh3)2 (98 mg, 0.14 mmol) and pent-1-en-3-one (1.08 ml, 1.08 mmol) were added at room temperature and the mixture was stirred at 130 degrees C for 16h. To the mixture, ethyl acetate was added and the organic layer was washed with H2O, dried over MgSO4, concentrated in vacuo. The obtained residue was purified by preparative TLC (n- hexane:ethyl acetate=1 :3) to give the title compound (353 mg). 1H-NMR: 0.61 (t, 6H), 1.17 (t, 3H), 2.04 (q, 4H), 2.37 (s, 3H), 2.69 (q, 2H), 6.63 (d, 1 H), 6.75 (d, 1 H), 6.98-7.05 (m, 2H), 7.45 (d, 1 H), 7.82 (d, 1 H); MS (ESI+) : 337 ([M+H]+).

(4) Preparation of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl - phenyl]-propyl}-phenol To a solution of (E)-1-{4-[1-ethyl-1-(4-hydroxy-phenyl)-propyl]-2-methyl-phen yl}- pent-1-en-3-one (350 mg, 1.04 mmol) in THF (2 ml), 0.5 M EtLi in THF (10.4 ml, 5.21 mmol) was added at 0 degree and the mixture was stirred at room temperature for 1 h. To the mixture, saturated NH4CI was added, flirted through celite and concentrated in vacuo. The residue was purified by preparative TLC (ethyl acetate/n-hexane = 1/2) to give the title compound (145 mg, 38%). 1H-NMR: 0.60 (t, 6H), 0.92 (t, 6H), 1.61 (q, 4H), 2.03 (q, 4H), 2.30 (s, 3H), 5.99 (d, 1 H), 6.70-7.28 (m, 8H); MS (ESI+): 349 ([M-OH]+).

Example 165 Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-phenoxy)-4-hydroxy-pentanoic acid

HOOC HO (1 ) Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-phenoxymethyl)-dihydro-furan-2-one

To a solution of 4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-phenol (compound prepared in Example 164-(4)) (135 mg, 0.369 mmol) in DMF (2 ml), K2CO3 (153 mg, 1.11 mmol) and (S)-(+)-dihydro-5-(p- tolenesulfonylmethyl)-2(3H)-furanone (150 mg, 0.554 mmol) were added at room temperature and the mixture was stirred at 100 degrees C for 16h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane to n-hexane:ethyl acetate=1 :1) to give the title compound (117 mg, 68%). 1H-NMR: 0.62 (t, 6H), 0.91 (t, 6H), 1.62-1.65 (q, 4H), 2.30 (s, 3H), 4.05-4.17 (m, 2H)1 4.82-4.89 (m, 1H), 6.01 (d, 1 H), 6.70-6.82 (m, 3H), 7.08 (d, 1H), 7.29(d, 1 H); MS (ESI+) : 465 ([M+H]+).

(2) Preparation of (S)-5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3 - methyl-phenyl]-propyl}-phenoxy)-4-hydroxy-pentanoic acid

o

To a solution of (S)-5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3 - methyl-phenyl]-propyl}-phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 165-(1)) (117 mg, 0.252 mmol) in MeOH (3 ml), 1 N NaOH (0.6 ml) were added at room temperature and the mixture was stirred at room temperature for 1h. The mixture was concentrated in vacuo, and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (59 mg, 49%). 1H-NMR: 0.61 (t, 6H), 0.91 (t, 6H), 1.63 (q, 4H), 2.02 (q, 4H), 2.17 (s, 3H), 2.66 (t, 2H), 3.79-3.89 (m, 1 H), 3.93-4.08 (m, 2H), 6.00 (d, 1 H), 6.72-7.31 (m, 8H); MS (ESI+) : 500 ([M+NH4]+).

Example 166 Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2,6-dimethyl-phenoxymethyl)-dihydro-f uran-2-one

(1 ) Preparation of 4-[1-(4-Bromo-3-methyl-phenyl)-1-ethyl-propyl]-2,6-dimethyl- phenol To a solution of 3-(4-Bromo-3-methyl-phenyl)-pentan-3-ol (compound prepared in Example 164-(1)) (200 mg, 0.780 mmol) and 2,6-dimethyl-phenol (285 mg, 2.34 mmol) in toluene (0.2 ml), AICI3 (52 mg, 0.390 mmol) was added and the mixture was stirred at room temperature for 60 h. The mixture applied onto silica and chromatographed (n-hexane:CH2Cl2=30:70 to 0:100) to give the title compound as mixture of 2,6-dimethyl-phenol (356 mg). 1H-NMR: 0.59 (t, 6H1 -CH2-CH3), 2.03 (q, 4H, -CH2-CH3); MS (ESI+) : 361 ([M+H]+).

(2) Preparation of (E)-1-{4-[1-Ethyl-1-(4-hydroxy-3,5-dimethyl-phenyl)-propyl]- 2- methyl-phenyl}-pent-1 -en-3-

one To a solution of 4-[1-(4-bromo-3-methyl-phenyl)-1-ethyl-propyl]-2,6-dimethyl- phenol prepared in Example 166-(1) (110 mg) in DMF (1 ml), NaHCO3 (81 mg, 0.96 mmol), LiBr (14.7 mg, 0.17 mmol), dppp (10 mg, 0.024 mmol), PdCI2(PPh3)2 (16.9 mg, 0.024 mmol) and pent-1-en-3-one (0.20 ml, 0.20 mmol) were added at room temperature and the mixture was stirred at 140 degrees C for 16h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (CH2CI2:MeOH=100:0 to 10:1 ) to give the title compound (85 mg). 1H-NMR: 0.60 (t, 6H)1 1.17 (t, 3H), 2.04 (q, 4H), 2.19 (s, 6H), 2.67 (q, 2H), 4.56 (s, 1H), 6.65 (d, 1 H), 6.73 (s, 1H), 6.98-7.03 (m, 2H), 7.46 (d, 1H), 7.80 (d, 1 H); MS (ESI+) : 365 ([M+H]+). (3) Preparation of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl - phenyl]-propyl}-2,6-dimethyl-phenol

To a solution of (E)-1-{4-[1-Ethyl-1-(4-hydroxy-3,5-dimethyl-phenyl)-propyl]- 2- methyl-phenyl}-pent-1-en-3-one (compound prepared in Example 166-(2)) (85 mg, 0.233 mmol) in THF (2 ml), 0.89 M EtMgBr in THF (1.63 ml, 1.35 mmol) was added at 0 degrees C and the mixture was stirred at room temperature for 1h. To the mixture, saturated NH4CI was added, the mixture was flirted through celite and concentrated in vacuo. The obtained residue was purified by preparative TLC (ethyl acetate/n-hexane = 1/4) to give the title compound (17 mg, 19%). 1H-NMR: 0.60 (t, 6H), 0.92 (t, 6H), 1.61 (q, 4H), 2.02 (q, 4H), 2.19 (s, 6H), 2.38 (s, 3H), 4.47 (s, 1H), 6.00 (d, 1H), 6.73-7.30 (m, 6H); MS (ESI+) : 395 ([M+H∏.

(4) Preparation of (S)-5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3 - methyl-phenyl]-propyl}-2,6-dimethyl-phenoxymethyl)-dihydro-f uran-2-

one To a solution of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl - phenyl]-propyl}-2,6-dimethyl-phenol (compound prepared in Example 166-(3)) (16 mg, 0.0406 mmol) in DMF (0.3 ml), K2CO3 (16.9 mg, 0.122 mmol) and (S)- (+)-dihydro-5-(p-tolenesulfonylmethyl)-2(3H)-furanone (21.9 mg, 0.0812 mmol) were added at room temperature and the mixture was stirred at 100 degrees C for 16h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=2:1) to give the title compound (16 mg, 80%). 1H-NMR: 0.60 (t, 6H), 0.92 (t, 6H), 1.65 (q, 4H), 2.05 (q, 4H)1 2.21 (s, 6H), 3.90- 4.01 (m, 2H), 4.78-4.82 (m, 1H), 6.02 (d, 1H), 6.75-7.30 (m, 5H); MS (ESI+): 510 ([M+NH4]+).

Example 167 Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2,6-dimethyl-phenoxy)-4-hydroxy-penta noic acid

HOOC HO Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2,6-dimethyl-phenoxy)-4-hydroxy-penta noic acid

To a solution of (S)-5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3 - methyl-phenyl]-propyl}-2,6-dimethyl-phenoxymethyl)-dihydro-f uran-2-one (compound prepared in Example 166-(4)) (11 mg, 0.022 mmol) in MeOH (0.3 ml), 1 N NaOH (0.1 ml) was added and the mixture was stirred at room temperature for 1 h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (4.7 mg, 41%). 1H-NMR: 0.60 (t, 6H), 0.92 (t, 6H), 1.64 (q, 4H), 2.02 (q, 4H), 2.21 (s, 6H), 2.34 (s, 3H), 2.61 (t, 2H), 3.66-3.79 (m, 2H), 4.01-4.10 (m, 1 H), 6.02 (d, 1 H), 6.72- 7.34(m, 6H); MS (ESI+): 528 ([M+NH4]+).

Example 168 Preparation of 4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-propyl- phenyl]-propyl}-2-methyl-phenol

(1 ) Preparation of 1-(4-Hydroxy-3-propyl-phenyl)-propan-1-one o

To a mixture of 2-propyl-phenol (2.0 g, 14.7 mmol) and propionyl chloride (1.36 g, 14.7 mmol), AICI3 (2.15 g, 16.2 mmol) was added and the mixture was stirred at room temperature for 1 h. The mixture was applied onto silica and chromatographed (ethyl acetate:n-hexane = 0:100 to 50:50) to give the title compound (0.30 g, 11%). 1H-NMR: 0.97 (t, 3H), 1.22 (t, 3H), 1.64 (q, 2H), 2.63 (t, 2H), 2.96 (q, 2H), 6.85 (d, 1 H), 7.72-7.79 (m, 2H); MS (ESI+): 193 ([M+H]+).

(2) Preparation of 4-(1-Ethyl-1-hydroxy-propyl)-2-propyl-phenol o

To a solution of 4-(1-ethyl-1-hydroxy-propyl)-2-propyl-phenol (compound prepared in Example 168-(1)) (0.30 g, 1.56 mmol) in THF (5 ml), 3M EtMgBr in diethyl ether (2.6 ml, 7.80 mmol) was added at 0 degrees C and the mixture was stirred at room temperature for 16h. To the mixture, H2O and ethyl acetate were added and the organic layer was washed with H2O, dried over MgSO4, concentrated in vacuo. The obtained residue was chromatographed on silica gel (ethyl acetate: n-hexane = 0:100 to 50:50) to give the title compound (0.32 g, O ). 1H-NMR: 0.76 (t, 6H), 0.96 (t, 3H), 1.77-1.83 (m, 4H), 2.58 (t, 2H), 4.68-4.71 (m, 1 H), 6.70 (d, 1 H), 7.02-7.07 (m, 2H).

(3) Preparation of Trifluoro-methanesulfonic acid 4-(1-ethyl-1-hydroxy-propyl)-2- propyl-phenyl ester

TfO

To a solution of 4-(1-ethyl-1-hydroxy-propyl)-2-propyl-phenol (compound prepared in Example 168-(2)) (315 mg, 1.42 mmol) in CH2CI2 (5 ml), pyridine (0.172 ml, 2.13 mmol) and trifluoromethanesulfonic anhydride (0.239 ml, 1.42 mmol) were added at 0 degrees C and the mixture was stirred at 0 degrees C for 2h. The mixture was applied onto silica and chromatographed (ethyl acetate:n- hexane = 0:100 to 50:50) to give the title compound (0.21 g, 42%). 1H-NMR: 0.67 (t, 6H), 0.97 (t, 3H), 1.78-1.83 (m, 4H), 2.65 (t, 2H), 7.16-7.32 (m, 3H).

(4) Preparation of Trifluoro-methanesulfonic acid 4-[1 -ethyl- 1-(4-hydroxy-3- methyl-phenyl)-propyl]-2-propyl-phenyl ester

πo OTf

To a mixture of 2-methyl-phenol (84 mg, 0.78 mmol) and trifluoro- methanesulfonic acid 4-(1-ethyl-1-hydroxy-propyl)-2-propyl-phenyl ester (compound prepared in Example 168-(3)) (138 mg, 0.39 mmol) in tolunene (0.3 ml), trifluoromethanesulfonic acid (0.040 ml) was added and the mixture was stirred at room temperature for 16h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=100:0 to 50:50) to give the mixture of the title compound containing 2-methyl-phenol (192 mg). 1H-NMR: 0.60 (t, 6H, -CH2CH3), 0.90 (t, 3H, -CH2CH2CH3), 1.65 (q, 2H, - CH2CH2CH3), 2.02 (q, 4H, -CH2CH3), 2.12 (s, 3H, Ph-CH3), 2.61 (t, 2H, - CH2CH2CH3); MS (ESI+) : 445 ([M+H]+).

(5) Preparation of (E)-1-{4-[1 -Ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2- propyl-phenyl}-pent-1-en-3-one

OTf

To a solution of compound prepared in Example 168-(4) (trifluoro- methanesulfonic acid 4-[1 -ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2-propyl- phenyl ester) (compound prepared in Example 168-(4)) (192 mg) in DMF (3 ml), NaHCO3 (131 mg, 1.56 mmol), LiBr (23.4 mg, 0.273 mmol), dppp (16.1 mg, 0.039 mmol), PdCI2(PPh3J2 (27.4 mg, 0.039 mmol) and pent-1 -en-3-one (0.381 ml, 3.12 mmol) were added at room temperature and the mixture was stirred at 130 degrees C for 64 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was purified by preparative TLC (n-hexane:ethyl acetate=3:1 ) to give the title compound (74 mg). 1H-NMR: 0.64 (t, 6H), 0.90 (t, 3H), 1.17 (t, 3H), 1.52 (q, 2H), 2.04 (q, 4H), 2.18 (s, 3H), 2.69 (q, 2H), 4.93 (s, 1 H), 6.62-6.66 (m, 2H), 6.82-6.86 (m, 1 H), 7.45 (d, 1 H), 7.85 (s, 1 H) MS (ESI+): 379 ([M+H]+).

(6) Preparation of 4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-propyl- phenyl]-propyl}-2-methyl-phenol To a solution of (E)-1-{4-[1 -Ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2- propyl-phenyl}-pent-1-en-3-one (compound prepared in Example 168-(5)) (70 mg, 0.185 mmol) in THF (2 ml), 0.5 M EtLi in THF (1.85 ml, 0.93 mmol) was added at 0 degree and the mixture was stirred at room temperature for 16h. To the mixture, saturated NH4CI was added, the products were extracted with ethyl acetate and the extracts were washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was purified by preparative TLC (n-hexane:ethyl acetate=5:1) to give the title compound (34 mg, 45%). 1H-NMR: 0.61 (t, 6H), 0.92 (t, 6H), 1.62 (q, 4H), 2.04 (q, 4H), 2.20 (s, 3H), 2.61 (t, 2H), 4.78 (s, 1 H), 6.00 (d, 1 H), 6.62 (d, 1 H), 6.73-6.95 (m, 1 H), 7.28 (d, 1 H); MS (ESI+) : 391 ([M-OH]+).

Example 169 Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- propyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

o

Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- propyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one To a solution of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-propyl - phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 168-(5)) (27 mg, 0.066 mmol) in DMF (0.5 ml), K2CO3 (27.3 mg, 0.198 mmol) and (SH+)- dihydro-5-(p-toluenesulfonylmethyl)-2(3H)-furanone (26.8 mg, 0.0991 mmol) were added at room temperature and the mixture was stirred at 100 degrees C for 16 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=2:1 ) to give the title compound (20 mg, 60%). 1H-NMR: 0.61 (t, 6H), 0.91 (t, 6H), 1.59 (q, 4H), 2.05 (q, 4H), 2.15 (s, 3H), 2.55- 2.63 (m, 2H), 4.02-4.20 (m, 2H), 4.83-4.93 (m ,1H), 6.00 (d, 1H), 6.63 (d, 1H), 6.78 (d, 1 H)1 7.25 (d, 1H); MS (ESI+): 524 ([M+NH4]+).

Example 170 Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- propyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

HOOC HO

Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- propyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

HOOC

To a solution of (S)-5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3 - propyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one (compound prepared in Example169) (16.8 mg, 0.033 mmol) in THF (1 ml) and MeOH (0.1 ml), 1 N NaOH (0.1 ml) was added and the mixture was stirred at room temperature for 1 h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3:Me0H=8:3 saturated with H2O) to give the title compound (12.4 mg, 72%). 1H-NMR: 0.61 (t, 6H), 0.91 (t, 6H), 1.60 (q, 4H), 2.02 (q, 4H), 2.15 (s, 3H), 3.80- 4.15 (m, 3H), 5.98 (d,1H), 6.66 (d, 1 H), 6.78 (d, 1 H), 6.87-6.93 (m, 2H); MS (ESI+) : 507 ([M-OH]+).

Example 171 Preparation of (S)-5-{4-[1 -(4-tert-Butylsulfanylmethyl-3-methyl-phenyl)-1 -ethyl- propyl]-2-methyl-phenoxymethyl}-dihydro-furan-2-one

o

(1 ) Preparation of 4-[1-Ethyl-1-(4-hydroxy-3-methyl-phenyl)-propyl]-2-methyl- benzoic acid methyl ester

OMe OTf

To a solution of trifluoro-methanesulfonic acid 4-[1-ethyl~1-(4-hydroxy-3-methyl- phenyl)-propyl]-2-methyl-phenyl ester (compound prepared in Example 1-(1)) (1480 mg, 3.554 mmol) in DMF (25 ml) and MeOH (25 ml), Pd(OAc)2 (240 mg, 1.069 mmol), dppp (440 mg, 1.067 mmol), and Et3N (1.3 ml, 9.321 mmol) were added at room temperature and the mixture was stirred at 100 degrees C for 16 h under CO gas. To the mixture, ethyl acetate was added and the mixture was washed with saturated ammonium chloride solution and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane/ethyl acetate =10/1 to 3/1 ) to give the title compound (363 mg, 31.3%). 1H-NMR (chloroform-d): 0.61 (t, 6H, J=7.2Hz), 2.07 (q, 4H, J=7.2Hz), 2.19 (s, 3H), 2.56 (s, 3H), 3.87 (s, 3H)1 4.88 (brs, 1 H), 6.66 (d, 1 H, J=8.1 Hz), 6.82-6.86 (m, 2H), 7.03-7.06 (m, 2H), 7.80 (d, 1 H, J=9.0Hz); MS (ESI+) : 349 ([M+Na]+). (2) Preparation of 4-{1-Ethyl-1-[3-methyl-4-(tetrahydro-pyran-2-yloxy)-phenyl]- propyl}-2-methyl-benzoic acid methyl ester

OMe OMe THPO

To a solution of 4-[1 -Ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2-methyl- benzoic acid methyl ester (compound prepared in Example 171-(1)) (220 mg, 0.674 mmol) in dichloromethane (1 ml), DHP (0.075 ml, 0.809 mmol) and PPTs (17 mg, 0.068 mmol) were added and the mixture was stirred at room temperature for 25.3 h. To the mixture, ethyl acetate was added and themixture was washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n- hexane/ethyl acetate =10/1 to 3/1 ) to give the title compound (243 mg, 87.8%) 1H-NMR (chloroform-d): 0.63 (t, 6H, J=7.3Hz), 1.55-1.76 (m, 3H), 1.85-1.88 (m, 2H), 1.95-2.13 (m, 1 H), 2.09 (q, 4H, J=7.3Hz), 2.21 (s, 3H), 2.58 (s, 3H), 3.59- 3.63 (m, 1 H), 3.87 (s, 3H), 3.91-3.98 (m, 1 H), 5.39 (t, 1 H, J=3.2Hz), 6.88-7.13 (m, 5H), 7.82 (d, 1 H, J=8.8Hz); MS (ESI+) : 433 ([M+Na∏.

(3) Preparation of (4-{1-Ethyl-1-[3-methyl-4-(tetrahydro-pyran-2-yloxy)-phenyl] - propyl}-2-methyl-phenyl)-methanol

OMe THPO THPO

To a solution of 4-{1-Ethyl-1-[3-methyl-4-(tetrahydro-pyran-2-yloxy)-phenyl]- propyl}-2-methyl-benzoic acid methyl ester (compound prepared in Example 171 -(2)) (177 mg, 0.431 mmol) in THF (2 ml), LAH (20 mg, 0.527 mmol) was added and the mixture was stirred at room temperature for 18 h. To the mixture, ethyl acetate and brine were added and the organic layer was filtered through celite, concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane/ethyl acetate =1/1) to give the title compound (165 mg, quant). 1 H-NMR (chloroform-d): 0.61 (t, 6H, J=7.3Hz), 1.58-1.74 (m, 4H), 1.84-1.89 (m, 2H), 2.06 (q, 4H, J=7.3Hz), 2.20 (s, 3H), 2.30 (s, 3H), 3.58-3.64 (m, 1 H), 3.90- 3.98 (m, 1 H), 4.66 (s, 2H), 5.37 (t, 1 H, J=3.3Hz), 6.89-7.03 (m, 5H), 7.20 (d, 1 H, J=7.9Hz).

(4) Preparation of 2-{4-[1-(4-Chloromethyl-3-methyl-phenyl)-1-ethyl-propyl]-2- methyl-phenoxy}-tetrahydro-pyran

THPO ^r T ^ THPO

To a solution of (4-{1-Ethyl-1-[3-methyl-4-(tetrahydro-pyran-2-yloxy)-phenyl] - propyl}-2-methyl-phenyl)-methanol (compound prepared in Example 171 -(3)) (178.3 mg, 0.466 mmol) in CH2CI2 (3 ml), MsCI (0.1 ml, 1.292 mmol), Et3N (325 ml, 2.33 mmol) and DMAP (6 mg, 0.049 mmol) were added at 0 degrees C and the mixture was stirred at 0 degrees C for 17 h. To the mixture, ethyl acetate was added and the mixture was washed with saturated sodium hydrogen carbonate solution and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. To the solution of the residue in DMF (1 ml), LiCI (20 mg, 0.472 mmol) was added and the mixture was stirred at room temperature for 2.5 h. To the mixture, ethyl acetate was added and the mixturer was washed with saturated ammonium chloride solution and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane/ethyl acetate =5/1 ) to give the title compound (137.9 mg, 73.8%). 1H-NMR (chloroform-d): 0.61 (t, 6H, J=7.3Hz), 1.57-1.75 (m, 4H), 1.85-1.90 (m, 2H), 0.00 (q, 4H, J=7.3Hz), 2.21 (s, 3H), 2.37 (s, 3H), 3.58-3.65 (m, 1 H), 3.90- 3.98 (m, 1 H), 4.60 (s, 2H), 5.38 (t, 1 H, J=3.3Hz), 6.89-7.00 (m, 5H), 7.18 (d, 1 H, J=8.8Hz); MS (ESI+) : 418 ([M+NH4]+). (5) Preparation of 2-{4-[1-(4-tert-Butylsulfanylmethyl-3-methyl-phenyl)-1-θthy l- propyl]-2-methyl-phenoxy}-tetrahydro-pyran

THPO THPO

To a solution of 2-{4-[1-(4-Chloromethyl-3-methyl-phenyl)-1-ethyl-propyl]-2- methyl-phenoxy}-tetrahydro-pyran (compound prepared in Example 171 -(4)) (96.2 mg, 0.24 mmol) in Acetone (3 ml), t-BuSH (334 mg, 3.71 mmol), KOH (212 mg, 3.79 mmol) in EtOH (6 ml) was added at room temperature and the mixture was stirred at 71 degrees C for 1 h. To the mixture, ethyl acetate was added and the mixture was washed with saturated sodium hydrogen carbonate solution and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane/ethyl acetate =7/1 to 3/1) to give the title compound (106.2 mg, 97.4%). 1H-NMR (chloroform-d): 0.60 (t, 6H, J=7.3Hz), 1.40 (s, 9H), 1.55-1.75 (m, 4H), 1.84-1.90 (m, 2H), 2.03 (q, 4H, J=7.3Hz), 2.20 (s, 3H), 2.36 (s, 3H), 3.55-3.65 (m, 1 H), 3.73 (s, 2H), 3.91-3.98 (m, 1 H), 5.37 (t, 1 H, J=3.2Hz), 6.89-6.99 (m, 5H), 7.13 (d, 2H1 J=8.5Hz); MS (ESI+) : 472([M+NH4]+).

(6) Preparation of (S)-5-{4-[1-(4-tert-Butylsulfanylmethyl-3-methyl-phenyl)-1- ethyl-propyl]-2-methyl-phenoxymethyl}-dihydro-furan-2-one

O THPO O y° To a solution of 2-{4-[1-(4-tert-Butylsulfanylmethyl-3-methyl-phenyl)-1-ethyl - propyl]-2-methyl-phenoxy}-tetrahydro-pyran (compound prepared in Example 171 -(5)) (106.2 mg, 0.234 mmol) in MeOH (3ml), Montmorillinite K-10 (60mg) was added and the mixture was stirred at room temperature for 17.5 h. To the mixture, ethyl acetate and brine were added and the organic layer was filtered through celite, concentrated in vacuo. To the solution of the residue in DMF (3 ml), toluene-4-sulfonic acid (S)-5-oxo-tetrahydro-furan-2-ylmethyl ester (140 mg, 0.515 mmol), K2CO3 (75 mg, 0.538 mmol) were added at room temperature and the mixture was stirred at 83 degrees C for 8 h. To the mixture, ethyl acetate was added and the mixture was washed with brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane/ethyl acetate =3/1 ) to give the title compound (71.2 mg, 64.9%) as colorless oil. 1H-NMR (chloroform-d): 0.58 (t, 6H, J=7.3Hz), 1.39 (s, 9H), 2.02 (q, 4H, J=7.3Hz), 2.15 (s, 3H), 2.35 (s, 3H), 2.27-2.62 (m, 3H), 2.77 (ddd, 1 H, J=7.3, 10.2, 17.6Hz), 3.72 (s, 2H), 4.06 (dd, 1 H, J=3.5, 10.4Hz), 4.16 (dd, 1H, J=3.5, 10.4Hz), 4.84-4.91 (m, 1 H), 6.65 (d, 1 H, J=8.2Hz), 6.90-6.95 (m, 4H), 7.12 (d, 1 H, J=8.5Hz); MS (ESI+) : 486 ([M+NH4∏.

Example 172 Preparation of (S)-5-{4-[1 -(4-tert-Butylsulfanylmethyl-3-methyl-phenyl)-1 -ethyl- propyl]-2-methyl-phenoxy}-4-hydroxy-pentanoic acid

o

Preparation of (S)-5-{4-[1 -(4-tert-Butylsulfanylmethyl-3-methyl-phenyl)-1 -ethyl- propyl]-2-methyl-phenoxy}-4-hydroxy-pentanoic acid

Γ

To a solution of (S)-5-{4-[1-(4-tert-Butylsulfanylmethyl-3-methyl-phenyl)-1-e thyl- propyl]-2-methyl-phenoxymethyl}-dihydro-furan-2-one (compound prepared in Example 171) (10 mg, 0.021 mmol) in MeOH (1 ml), 1 N KOH aqueous solution (0.12 ml, 0.12 mmol) was added and stirred at room temperature for 12 h. The mixture was concentrated in vacuo and purified by preparative TLC (chroloform/methanol =8/3, saturated by water) to give the title compound (5.5 mg, 53%). 1H-NMR (chloroform-d): 0.60 (t, 3H, J=7.5Hz), 1.39 (s, 9H), 1.88-2.12 (m, 2H), 2.04 (q, 4H, J=7.5Hz), 2.18 (s, 3H), 2.36 (s, 3H), 2.63 (brt, 2H, J=7.2Hz), 3.73 (s, 2H), 3.86 (dd, 1 H, J=6.8, 9.2Hz), 3.99 (dd, 1 H, J=3.5, 9.2Hz), 4.05-4.13 (m, 1 H), 6.68 (d, 1H1 J=8.3Hz), 6.92-6.96 (m, 4H), 7.14 (d, 1 H, J=8.5Hz); MS (ESI+) : 504 ([M+NH4]+).

Example 173 Preparation of 5(S)-(4-{1 -Ethyl-1 -[3-methyl-4-(2-methyl-propane-2- sulfinylmethyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihy dro-furan-2-one

Preparation of 5(S)-(4-{1 -Ethyl-1 -[3-methyl-4-(2-methyl-propane-2- sulfinylmethyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihy dro-furan-2-one

o

To a solution of (S)-5-{4-[1-(4-tert-Butylsulfanylmethyl-3-methyl-phenyl)-1-e thyl- propyl]-2-methyl-phenoxymethyl}-dihydro-furan-2-one (compound prepared in Example 171) (20 mg, 0.043 mmol) in CH2CI2 (6 ml), mCPBA (>65%) (10.75 mg, 0.041 mmol) in CH2CI2 (2 ml) was added slowly at -78 degrees C and the mixture was stirred at -78 degrees C for 7 min. The mixture was concentrated in vacuo and purified by preparative TLC (n-hexane/ethyl acetate =1/99) to give the title compound (18.7 mg, 90.4%). 1H-NMR (chloroform-d): 0.59 (t, 6H, J=7.3Hz), 1.34 (s, 9H), 2.04 (q, 4H, J=7.3Hz), 2.16 (s, 3H), 2.30 (s, 3H), 2.26-2.62 (m, 3H), 2.77 (ddd, 1 H, J=7.1 , 10.3, 17.2Hz), 3.59 (d, 1 H, J=12.9Hz), 3.88 (d, 1 H, J=12.7Hz), 4.04-4.19 (m, 2H), 4.85-4.91 (m, 1 H), 6.66 (d, 1 H, J=8.3Hz), 6.91-7.00 (m, 4H), 7.15 (d, 1 H, J=7.9Hz); MS (ESI+) : 485 ([M+H∏.

Example 174 Preparation of 5-(4-{1 -Ethyl-1 -[3-methyl-4-(2-methyl-propane-2-sulfinylmethyl)- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

O

Preparation of 5-(4-{1 -Ethyl-1 -[3-methyl-4-(2-methyl-propane-2-sulfinylmethyl)- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid I ^^ IJL s / O HCT^- OH -JY

To a solution of 5(S)-(4-{1-Ethyl-1-[3-methyl-4-(2-methyl-propane-2- sulfinylmethyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihy dro-furan-2-one (compound prepared in Example 173) (10 mg, 0.021 mmol) in MeOH (1 ml), 1 N KOH aqueous solution (0.12 ml, 0.124 mmol) was added and the mixture was stirred at room temperature for 12 h. The mixture was concentrated in vacuo and purified by preparative TLC (chroloform/methanol =8/3, saturated by water) to give the title compound (2.3 mg, 22.2%). 1H-NMR (chloroform-d): 0.60 (t, 6H, J=7.3Hz), 1.34 (s, 9H), 1.85-1.98 (m, 2H), 2.05 (q, 4H, J=7.3Hz), 2.18 (s, 3H), 2.31 (s, 3H), 2.59 (t, 2H, J=7.2Hz), 3.60 (d, 1 H, J=13.0Hz), 3.89 (d, 1 H, J=13.2Hz), 3.83-4.00 (m, 2H), 4.03-4.09 (m, 1 H), 6.68 (d, 1 H, J=8.8Hz), 6.91-6.98 (m, 4H), 7.15 (d, 1 H, J=8.3Hz); MS (ESI+) : 503 ([M+H]+). Example 175 Preparation of (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(2-methyl-propane-2- sulfonylmethyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-clih ydro-furan-2-one

O

Preparation of (S)-5-(4-{1 -Ethyl-1-[3-methyl-4-(2-methyl-propane-2- sulfonylmethyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihy dro-furan-2-one

r- Ό o d To a solution of (S)-5-{4-[1-(4-tert-Butylsulfanylmethyl-3-methyl-phenyl)-1-e thyl- propyl]-2-methyl-phenoxymethyl}-dihydro-furan-2-one (compound prepared in Example 171 ) (20 mg, 0.043 mmol) in CH2CI2 (6 ml), mCPBA (>65%) (20 mg, 0.085 mmol) in CH2CI2 (2 ml) was added slowly at 0 degrees C and the mixture was stirred at 0 degrees C for 0.5 h. The mixture was concentrated in vacuo and purified by preparative TLC (n-hexane/ethyl acetate =3/1 ) to give the title compound (20.3 mg, 95%). 1H-NMR (chloroform-d): 0.59 (t, 6H, J=7.4Hz), 1.49 (s, 9H), 2.04 (q, 4H1 J=7.4Hz), 2.16 (s, 3H), 2.37 (s, 3H), 2.26-2.62 (m, 3H), 2.77 (ddd, 1 H1 J=7.0, 10.2, 17.2Hz), 4.04-4.20 (m, 2H), 4.20 (s, 2H), 4.85-4.91 (m, 1H), 6.66 (d, 1H, J=8.2Hz), 6.92-7.01 (m, 4H), 7.23 (d, 1 H, J=8.5Hz); MS (ESI+) : 518 ([M+NH4f).

Example 176 Preparation of (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(2-methyl-propane-2- sulfonylmethyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy- pentanoic acid O

Preparation of (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(2-methyl-propane-2- sulfonylmethyl)-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy- pentanoic acid

O w I l * O VS O

To a solution of (S)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(2-methyl-propane-2- sulfonylmethyl)-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihy dro-furan-2-one (compound prepared in Example 175) (10 mg, 0.02 mmol) in MeOH (1 ml), 1 N KOH aqueous solution (0.12 ml, 0.12 mmol was added and the mixture was stirred at room temperature for 12 h. The mixture was concentrated in vacuo and purified by preparative TLC (chroloform/methanol=8/3, saturated by water) to give the title compound (4.3 mg, 41.5%). 1H-NMR (chloroform-d): 0.60 (t, 6H, J=7.3Hz), 1.49 (s, 9H), 1.83-2.14 (m, 2H), 0.00 (q, 4H, J=7.3Hz), 2.17 (s, 3H), 2.37 (s, 3H), 2.62 (t, 2H, J=7.5Hz), 3.85 (dd, 1 H, J=6.8, 9.3Hz), 3.97 (dd, 1 H, J=3.6, 9.3Hz), 4.04-4.11 (m, 1 H), 4.20 (s, 2H), 6.68 (d, 1 H, J=8.3Hz), 6.91-7.02 (m, 4H), 7.23 (d, 1 H, J=8.5Hz); MS (ESI+) : 536 ([M+NH4]+).

Example 177 Preparation of 5(S)-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-dec-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one (1) Preparation of (E)-1-{4-[1 -Ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenyl}-pent-1 -en-3-one

OTf

To a solution of compound prepared in Example 1-(1) (trifluoro-methanesulfonic acid 4-[1 -ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2-methyl-phenyl ester) (100 mg, 0.24 mmol) in DMF (1 ml), NaHCO3 (80.6 mg, 0.96 mmol), LiBr (14.6 mg, 0.17 mmol), dppp (9.9 mg, 0.024 mmol), PdCI2(PPh3)2 (16.8 mg, 0.024 mmol) and acrylic acid methyl ester (0.20 ml, 2.0 mmol) were added at room temperature and the mixture was stirred at 150 degrees C for 5h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=100:0 to 70:30) to give the title compound (33 mg, 39%). 1H-NMR: 0.61 (t, 6H), 1.13 (t, 3H), 2.02 (q, 4H), 2.15 (s, 3H), 2.37 (s, 3H), 3.75 (s, 1H), 6.58 (m ,2H), 6.78-6.83 (m, 2H), 6.97-7.02 (m, 2H), 7.45 (d, 1H), 7.81 (d, 1H); MS (ESI+) : 351 ([M+H]+).

(2) Preparation of 4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-dec-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

To a solution of (E)-1-{4-[1 -ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2-methyl- phenyl}-pent-1-en-3-one (compound prepared in Example 177-(1 )) (70 mg, 0.200 mmol) in THF (2 ml), 1 M heptyl magnesium bromide in THF (0.80 ml, 0.80 mmol) was added at 0 degrees C and the mixture was stirred at 0 degrees C for 30min and at room temperature for 2h. To the mixture, saturated NH4CI solutionwas added and the mixture was filtrated through celite, concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=100:0 to 50:50) to give the title compound (17 mg, 19%). 1H-NMR: 0.61 (t, 6H)1 0.83-0.94 (m, 6H), 2.02 (q, 4H), 2.19 (s, 3H), 2.29 (s, 3H), 4.73 (s, 1H), 6.02 (d, 1H), 6.62-7.31 (m, 7H); MS (ESI+) : 433 ([M-OH]+).

(3) Preparation of 5(S)-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-dec-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

To a solution of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-dec-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 177-(2)) (17 mg, 0.0378 mmol) in DMF (0.3 ml), K2CO3 (15.7 mg, 0.113 mmol) and (S)-(+)- dihydro-5-(p-toluenesulfonylmethyl)-2(3H)-furanone (20.4 mg, 0.0756 mmol) were added at room temperature and the mixture was stirred at 110 degrees C for 16h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO-1, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=100:0 to 5:1 ) to give the title compound (10.5 mg, 51%). 1H-NMR: 0.60 (t, 6H), 0.82-0.92 (m, 6H), 2.02 (q, 4H), 2.17 (s, 3H), 2.32 (s, 3H), 4.02-4.18 (m, 2H), 4.84-4.91 (m, 1 H), 6.01 (d, 1 H), 6.63-6.75 (m ,2H), 6.91-6.98 (m, 4H), 7.29 (d, 1 H); MS (ESI+) : 566 ([M+NH4]+).

Example 178 Preparation of 5(S)-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-undec-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one (1) Preparation of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-undec-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol

To a solution of (E)-1-{4-[1-ethyl-1-(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenyl}-pent-1-en-3-one (compound prepared in Example 177-(1)) (70 mg, 0.200 mmol) in THF (2 ml), 2M octyl magnesium bromide in THF (0.40 ml, 0.80 mmol) were added at 0 degrees C and the mixture was stirred at 0 degrees C for 30min and at room temperature for 2h. To the mixture, saturated NH4CI solutionwas added and the mixture was filtrated through celite and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n- hexane:ethyl acetate=100:0 to 50:50) to give the title compound (22 mg, 24%). 1H-NMR: 0.60 (t, 6H), 0.80-0.90 (m, 6H), 2.02 (q, 4H), 2.19 (s, 3H), 2.29 (s, 3H), 6.02 (d, 1H), 6.61-7.30 (m, 7H); MS (ESI+) : 447 ([M-OH]+).

(2) Preparation of 5(S)-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-undec-1-enyl)-3 - methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

To a solution of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-undec-1-enyl)-3-methy l- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 178-(1)) (22 mg, 0.0474 mmol) in DMF (0.3 ml), K2CO3 (19.7 mg, 0.144 mmol) and (S)-(+)- dihydro-5-(p-toluenesulfonylmethyl)-2(3H)-furanone (25.6 mg, 0.0948 mmol) were added at room temperature and the mixture was stirred at 110 degrees C for 16h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=100:0 to 5:1) to give the title compound (9.9 mg, 37%). 1H-NMR: 0.61 (t, 6H), 0.84-0.93 (m, 6H), 2.04 (q, 4H), 2.15 (s, 3H), 2.32 (s, 3H)1 4.02-4.18 (m, 2H), 4.84-4.91 (m, 1 H), 6.01 (d, 1 H), 6.63-6.75 (m ,2H), 6.91-6.98 (m, 4H), 7.29 (d, 1H); MS (ESI+) : 580 ([M+NH4]+).

Example 179 Preparation of 5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-hex-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

HOOC OH (1 ) Preparation of 4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-hex-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

To a solution of (E)-1-{4-[1-Ethyl-1-(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenyl}-pent-1-en-3-one (compound prepared in Example 177-(1)) (70 mg, 0.200 mmol) in THF (2 ml), 0.93M n-propyl magnesium bromide in THF (1.08 ml, 1.00 mmol) were added at 0 degrees C and the mixture was stirred at 0 degrees C for 30min and at room temperature for 2h. To the mixture, saturated NH4CI solution was added and the mixture was filtrated through celite, concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=100:0 to 50:50) to give the title compound (37 mg, 47%). 1H-NMR: 0.57 (t, 6H), 0.83-0.92 (m, 6H), 2.00 (q, 4H), 4.98 (s, 1 H), 6.01 (d, 1 H), 6.61-7.30 (m, 7H). (2) Preparation of 5(S)-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-hex-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-prienoxymethyl)-dihydro-fura n-2-one

To a solution of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-undec-1-enyl)-3-methy l- phenyl]-propyl}-2-methyl-phenol compound prepared in Example 179-(1)) (18 mg, 0.0457 mmol) in DMF (0.4 ml), K2CO3 (16.6 mg, 0.120 mmol) and (S)-(+)- dihydro-5-(p-toluenesulfonylmethyl)-2(3H)-furanone (24.3 mg, 0.090 mmol) were added at room temperature and the mixture was stirred at 100 degrees C for 60 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethylacetate=100:0 to 5:1) to give the title compound (13 mg, 58%). 1H-NMR: 0.60 (t, 6H), 0.89-0.95 (m, 6H), 2.04 (q, 4H), 2.16 (s, 3H), 2.30 (s, 3H), 4.01-4.18 (m, 2H), 4.83-4.90 (m, 1H), 6.00 (d, 1 H), 6.63-6.75 (m ,2H), 6.89-6.97 (m, 4H), 7.29 (d, 1 H); MS (ESI+) : 475 ([M-OH]+).

(3) Preparation of 5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-hex-1-enyl)-3-meth yl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

HOOC OH

To a solution of 5(S)-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-hex-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one (compound prepared in Example 179-(2)) (13 mg, 0.026 mmol) in MeOH (1 ml), 1 N NaOH (0.1 ml) was added at room temperature and the mixture was stirred at room temperature for 1h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (2.0 mg, 15%). 1H-NMR: 0.60 (t, 6H), 0.87-0.92 (m, 6H), 2.01 (q, 4H), 2.18 (s, 3H), 2.30 (s, 3H), 2.59 (t, 2H), 3.80-4.07 (m, 3H), 6.01 (d,1H), 6.64-6.75 (m, 2H), 6.88-6.97 (m, 4H), 7.25 (d, 1 H); MS (ESI+) : 528 ([M+NH4]+).

Example 180 Preparation of 5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-hept-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

HOOC OH (1) Preparation of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-hept-1-enyl)-3-methyl - phenyl]-propyl}-2-methyl-phenol

To a solution of (E)-1-{4-[1 -Ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenyl}-pent-1-en-3-one (compound prepared in Example 177-(1)) (70 mg, 0.200 mmol) in THF (2 ml), 1.58M n-butyl lithium in n-hexane (0.632 ml, 1.00 mmol) were added at 0 degrees C and the mixture was stirred at 0 degrees C for 30min and at room temperature for 2h. To the mixture, saturated NH4CI solution was added and the mixture was filtrated through celite, concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=100:0 to 50:50) to give the title compound (51 mg, 62%). 1H-NMR: 0.61 (t, 6H)1 0.82-0.92 (m, 6H), 2.01 (q, 4H)1 2.18 (s, 3H), 2.30 (s, 3H), 4.95 (s, 1 H), 6.00 (d, 1 H), 6.62-7.30 (m, 7H); MS (ESI+) : 409 ([M+H]+). (2) Preparation of 5(S)-(4-{1-Ethyl-i-[4-((E)-3-ethyl-3-hydroxy-hept-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2- one

To a solution of 4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-hept-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 180-(1 )) (18 mg, 0.0441 mmol) in DMF (0.4 ml), K2CO3 (16.6 mg, 0.120 mmol) and (S)-(+)- dihydro-5-(p-toluenesulfonylmethyl)-2(3H)-furanone (24.3 mg, 0.090 mmol) were added at room temperature and the mixture was stirred at 100 degrees C for 60 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethylacetate=100:0 to 5:1 ) to give the title compound (20 mg, 90%). 1H-NMR: 0.60 (t, 6H), 0.89-0.92 (m, 6H), 2.02 (q, 4H), 2.17 (s, 3H), 2.28 (s, 3H), 4.02-4.18 (m, 2H), 4.82-4.90 (m, 1 H), 6.01 (d, 1 H), 6.64-6.75 (m ,2H), 6.89-6.95 (m, 4H), 7.25 (d, 1 H); MS (ESI+) : 489 ([M-OH]+).

(3) Preparation of 5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-hept-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentan oic acid

HOOC OH

To a solution of 5(S)-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-hept-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one (compound prepared in Example 180-(2)) (20 mg, 0.040 mmol) in MeOH (1 ml), 1 N NaOH (0.1 ml) was added and the mixture was stirred at room temperature for 1 h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (7.1 mg, 34%). 1H-NMR: 0.61 (t, 6H), 0.87-0.92 (m, 6H), 2.01 (q, 4H), 2.17 (s, 3H), 2.30 (s, 3H), 2.61 (t, 2H)1 3.80-4.10 (m, 3H), 6.01 (d,1H), 6.63-6.75 (m, 2H), 6.83-6.96 (m, 4H), 7.26 (d, 1 H); MS (ESI+) : 542 ([M+NH4]+).

Example 181 Preparation of 5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-oct-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

HOOC

(1) Preparation of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-oct-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

To a solution of (E)-1-{4-[1 -Ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenyl}-pent-1-en-3-one (compound prepared in Example 177-(1)) (70 mg, 0.200 mmol) in THF (2 ml), 2M pentyl magnesium bromide in THF (0.500ml, 1.OOmmol) was added at 0 degrees C and the mixture was stirred at 0 degrees C for 30min and at room temperature for 2h. To the mixture, saturated NH4CI solution was added and the mixture was filtrated through celite, concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=100:0 to 50:50) to give the title compound (23 mg, 27%). 1H-NMR: 0.60 (t, 6H), 0.80-0.90 (m, 6H), 2.00 (q, 4H), 2.17 (s, 3H), 2.28 (s, 3H), 4.88 (s, 1 H), 6.00 (d, 1 H), 6.60-7.28 (m, 7H); MS (ESI+) : 423 ([M+H]+).

(2) Preparation of 5(S)-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-oct-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2- one

To a solution of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-oct-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound preprared in Example 181-(1 )) (18 mg, 0.0427 mmol) in DMF (0.4 ml), K2CO3 (16.6 mg, 0.120 mmol) and (S)-(+)- dihydro-5-(p-toluenesulfonylmethyl)-2(3H)-furanone (24.3 mg, 0.090 mmol) were added at room temperature and the mixture was stirred at 100 degrees C for 60 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethylacetate=100:0 to 5:1 ) to give the title compound (22 mg, 99%). 1H-NMR: 0.61 (t, 6H), 0.83-0.92 (m, 6H), 2.03 (q, 4H), 2.12 (s, 3H), 2.30 (s, 3H), 4.01-4.18 (m, 2H), 4.83-4.90 (m, 1 H), 5.98 (d, 1 H), 6.60-6.72 (m ,2H), 6.82-6.95 (m, 4H), 7.25 (d, 1 H); MS (ESI+) : 503 ([M-OH]+).

(3) Preparation of 5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-oct-1-enyl)-3-meth yl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

HOOC OH

To a solution of (S)-5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-oct-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one (compound prepared in Example 181 -(2)) (22 mg, 0.042 mmol) in MeOH (1 ml), 1 N NaOH (0.1 ml) was added and the mixture was stirred at room temperature for 1 h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (1.8 mg, 8%). 1H-NMR: 0.60 (t, 6H), 0.82-0.90 (m, 6H), 2.03 (q, 4H), 2.18 (s, 3H), 2.30 (s, 3H), 2.59 (t, 2H), 3.80-4.13 (m, 3H), 6.00 (d,1H), 6.65-6.75 (m, 2H), 6.90-7.00 (m, 4H), 7.26 (d, 1H); MS (ESI+) : 556 ([M+NH4]+).

Example 182 Preparation of 5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-non-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

HOOCk ^\/^~o' OH (1) Preparation of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-non-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl- phenol

To a solution of (E)-1-{4-[1 -Ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenyl}-pent-1-en-3-one (compound prepared in Example 177-(1)) (70 mg, 0.200 mmol) in THF (2 ml), 2M hexyl magnesium bromide in THF (0.500 ml, 1.00 mmol) were added at 0 degrees C and the mixture was stirred at 0 degrees C for 30 min and at room temperature for 2 h. To the mixture, saturated NH4CI solution was added and the mixture was filtrated through celite, concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=100:0 to 50:50) to give the title compound (15 mg, 17%). 1H-NMR: 0.62 (t, 6H), 0.82-0.90 (m, 6H), 2.00 (q, 4H), 2.17 (s, 3H), 2.28 (s, 3H), 4.70 (s, 1 H), 6.00 (d, 1H), 6.60-7.28 (m, 7H); MS (ESI+) : 437 ([M+H]+).

(2) Preparation of 5(S)-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-non-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2- one

To a solution of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-non-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 182-(1)) (18 mg, 0.0413 mmol) in DMF (0.4 ml), K2CO3 (16.6 mg, 0.120 mmol) and (S)-(+)- dihydro-5-(p-toluenesulfonylmethyl)-2(3H)-furanone (24.3 mg, 0.090 mmol) were added at room temperature and the mixture was stirred at 100 degrees C for 60 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethylacetate=100:0 to 5:1 ) to give the title compound (17 mg, 77%). 1H-NMR: 0.62 (t, 6H), 0.82-0.92 (m, 6H), 2.05 (q, 4H), 2.15 (s, 3H), 2.30 (s, 3H), 4.01-4.18 (m, 2H), 4.82-4.90 (m, 1 H), 6.00 (d, 1 H), 6.61-6.72 (m ,2H), 6.88-6.95 (m, 4H), 7.26 (d, 1 H); MS (ESI+) : 517 ([M-OH]+).

(3) Preparation of 5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-non-1-enyl)-3-meth yl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

To a solution of 5(S)-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-non-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one (compound prepared in Example 182-(2)) (17 mg, 0.032 mmol) in MeOH (1 ml), 1 N NaOH (0.1 ml) was added and the mixture was stirred at room temperature for 1 h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (6.1 mg, 35%). 1H-NMR: 0.62 (t, 6H), 0.84-0.94 (m, 6H), 2.03 (q, 4H), 2.18 (s, 3H), 2.30 (s, 3H), 2.61 (t, 2H), 3.80-4.10 (m, 3H), 6.01 (d,1 H), 6.65-6.77 (m, 2H), 6.90-6.97 (m, 4H), 7.26 (d, 1 H); MS (ESI+) : 570 ([M+NH4]+).

Example 183 Preparation of 5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-dec-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

HOOC OH Preparation of 5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-dec-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

To a solution of compound prepared in Example 177-(3) ((S)-5-(4-{1 -Ethyl-1 -[4- ((E)-3-ethyl-3-hydroxy-dec-1-enyl)-3-methyl-phenyl]-propyl}- 2-methyl- phenoxymethyl)-dihydro-furan-2-one) (6.3 mg, 0.011 mmol) in MeOH (1 ml), 1 N NaOH (0.1 ml) was added and the mixture was stirred at room temperature for 1 h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (4.9 mg, 79%). 1H-NMR: 0.60 (t, 6H), 0.86-0.92 (m, 6H), 2.01 (q, 4H), 2.12 (s, 3H), 2.30 (s, 3H), 2.57 (t, 2H), 3.80-4.08 (m, 3H), 6.00 (d,1 H), 6.63-6.78 (m, 2H), 6.88-6.93 (m, 4H); MS (ESI+): 584 ([M+NH4]+).

Example 184 Preparation of 5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-undec-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid HOOC OH Preparation of 5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-undec-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentanoic acid

OH To a solution of 5(S)-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-undec-1-enyl)-3 - methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid (compound prepared in Example 178-(2)) (7.0 mg, 0.012 mmol) in MeOH (1 ml), 1 N NaOH (0.1 ml) was added and the mixture was stirred at room temperature for 1 h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (3.7 mg, 55%). 1H-NMR: 0.60 (t, 6H), 0.84-0.92 (m, 6H), 2.01 (q, 4H), 2.15 (s, 3H)1 2.30 (s, 3H), 2.58 (t, 2H), 3.80-4.07 (m, 3H), 6.00 (d,1 H), 6.62-6.72 (m, 2H), 6.85-6.93 (m, 4H); MS (ESI+) : 598 ([M+NH4]+).

Example 185 Preparation of 5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-oct-1 -en-4-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentan oic acid

HOOC OH (1) Preparation of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-oct-1-en-4-ynyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol To a solution of 1-pentyne (0.0986 ml, 1.00 mmol) in THF (1 ml), 1.56M n-butyl lithium in n-hexane (0.646 ml, 1.02 mmol) was added at 0 degrees C and the mixture was stirred at room temperature for 30min. To the mixture, a solution of 4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-oct-1 -en-4-ynyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenol (compound prepared in Example 177-(1)) (70 mg, 0.20 mmol) in THF (1 ml) was added at room temperature and the mixture was stirred at room temperature for 1 h. To the mixture, saturated NH4CI solution was added and the mixture was filtrated through celite, concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=100:0 to 50:50) to give the title compound (70 mg, 84%). 1H-NMR: 0.59 (t, 6H), 2.00 (q, 4H), 2.19 (s, 3H), 2.24 (t, 2H), 2.30 (s, 3H), 4.67 (s, 1 H), 6.05 (d, 1 H), 6.63 (d, 1 H), 6.82-6.95 (m, 4H), 7.08 (d, 1 H)1 7.36 (d, 1 H); MS (ESI+) : 419 ([M+H]+).

(2) Preparation of 5(S)-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-oct-1-en-4- ynyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2- one

To a solution of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-oct-1-en-4-ynyl)-3-me thyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 185-(1)) (15 mg, 0.0359 mmol) in DMF (0.4 ml), K2CO3 (16.6 mg, 0.120 mmol) and (S)-(+)- dihydro-5-(p-toluenesulfonylmethyl)-2(3H)-furanone (24.3 mg, 0.090 mmol) were added at room temperature and the mixture was stirred at 100 degrees C for 60 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (n-hexane:ethyl acetate=100:0 to 5:1) to give the title compound (18 mg, 97%). 1H-NMR: 0.59 (t, 6H), 0.97-1.04 (m, 6H), 2.03 (q, 4H), 2.16 (s, 3H), 2.27 (t, 2H), 2.32 (s, 3H), 4.01-4.18 (m, 2H), 4.82-4.90 (m, 1H), 6.03 (d, 1H), 6.62 (d, 1H), 6.90-6.97 (m, 4H), 7.03 (d, 1H), 7.37 (d, 1H) MS (ESI+): 499 ([M-OH]+)

(3) Preparation of 5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-oct-1-en-4-ynyl)-3 - methyl-phenyl]-propyl}-2-methyl-phenoxy)-4(S)-hydroxy-pentan oic acid

■σ HOOC OH To a solution of 5(S)-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-oct-1-en-4-ynyl )-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one (compound prepared in Example 185-(2)) (18 mg, 0.035 mmol) in MeOH (1 ml), 1N NaOH (0.1 ml) was added and the mixture was stirred at room temperature for 1 h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (5.2 mg, 29%). 1H-NMR: 0.60 (t, 6H)1 0.97-1.03 (m, 6H), 1.52-1.60 (m, 4H), 2.02 (q, 4H), 2.17 (s, 3H), 2.28 (t, 2H), 2.30 (s, 3H)1 2.62 (t, 2H)1 3.82-4.08 (m, 3H)1 6.08 (d, 1 H), 6.68 (d, 1 H)1 6.88-6.92 (m, 4H), 7.08 (d, 1 H)1 7.32 (d, 1 H); MS (ESI+) : 552 ([M+NH4]+).

Example 186 Preparation of 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5(S)-hydroxy-hexanoic acid

o (1 ) Preparation of 4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pen tyl]- 3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenol

OH i i OTBS To a solution of 4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 20) (5.04 g, 13.2 mmol) in CH2CI2 (40 ml) and lutidine (4.76 ml, 40.9 mmol), Trifluoromethanesulfonic acid tert-butyldimethylsilyl ester (0.51 ml, 3.09 mmol) was added at 0 degrees C and the mixture was stirred for 0.5 h at 0 degrees C. The reaction mixture was poured into H2O and the products were extracted with ethyl acetate and hexane. The extracts were washed with saturated aqueous NH4CI, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (ethyl acetate/hexane=0/100 to 10/90) to give the disilylated compound (7.32 g). This disilylated compound was dissolved with THF (113 ml) and 1 M TBAF in THF solution (12.6 ml, 12.6 mmol) was added at 0 degrees C and the mixture was stirred for 5 min at 0 degrees C. The reaction mixture was poured into brine and the products were extracted with ethyl acetate and hexane. The extracts were washed with brine twice, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (ethyl acetate/hexane=10/90 to 20/80) to give the title compound (5.66 g, 86%). 1H-NMR: 0.07 (s, 3H), 0.10 (s, 3H), 0.60 (t, 6H), 0.88 (s, 9H), 0.93 (s, 9H), 1.51- 1.63 (m, 1 H), 1.73-1.84 (m, 1 H), 2.03 (q, 4H), 2.20 (s, 3H), 2.23 (s, 3H), 2.36- 2.46 (m, 1H), 2.71-2.81 (m, 1H), 3.34 (dd, 1 H), 4.50 (s, 1H), 6.64 (d, 1 H), 6.85- 6.99 (m, 5H).

(2) Preparation of 6(S)-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimeth yl- pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxymet hyl]-tetrahydro- pyran-2-one To a solution of 4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pen tyl]-3- methyl-phenyl}-1-ethyl-propy|)-2-methyl-phenol (compound prepared in Example 186-(1)) (55.7 mg, 0.112 mmol), PPh3 (88.2 mg, 0.336 mmol), (S)-6- Hydroxymethyl-tetrahydro-pyran-2-one (J. Chem. Soc, Perkin Trans. 1, 2000, 20, 3519.) (43.7 mg, 0.336 mmol) in THF (0.2 ml), DEAD (58.6 mg, 0.336 mmol) was added slowly and the mixture was stirred at room temperature for 15 h. The mixture was concentrated in vacuo and purified by preparative TLC (n- hexane/ethyl acetate =1/1 and 3/1) to give the title compound (5.9 mg, 8.6%). 1H-NMR (chloroform-d): 0.07 (s, 3H), 0.11 (s, 3H), 0.60 (t, 6H, J=7.3Hz), 0.88 (s, 9H), 0.94 (s, 9H), 1.72-2.13 (m, 6H), 2.04 (q, 4H, J=7.3Hz), 2.16 (s, 3H), 2.24 (s, 3H), 2.36-2.81 (m, 4H), 3.34 (dd, 1 H, J=3.2Hz), 4.04 (dd, 1 H, J=5.6, 9.8Hz), 4.13 (dd, 1 H, J=4.3, 9.8Hz), 4.64-4.71 (m, 1 H), 6.67 (d, 1 H, J=8.3Hz), 6.89-7.00 (m, 5H).

(3) Preparation of 6-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5(S)-hydroxy-hexanoic acid

o To a solution of 6(S)-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimeth yl- pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxymet hyl]-tetrahydro- pyran-2-one (compound prepared in Example 186-(2)) (5.9 mg, 0.01 mmol) in THF (0.1 ml), 1.0M TBAF (0.24 ml, 0.24 mmol) was added and the mixture was stirred at 70 degrees C for 7 h. To the mixture, ethyl acetate was added and the mixture was washed with diluted potassium hydrogen sulfate aq., saturated sodium hydrogen carbonate solution, and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (dichrolomethane/methanol =15/1 ) to give the title compound (2.6 mg, 52.3%). 1H-NMR (methanol-d4): 0.58 (t, 6H, J=7.3Hz), 0.82 (s, 9H), 1.45-1.84 (m, 6H), 0.00 (q, 4H, J=7.3Hz), 2.14 (s, 3H), 2.23 (s, 3H), 2.34 (t, 2H, J=7.2Hz), 2.48-2.58 (m, 1 H), 2.81-2.91 (m, 1 H), 3.15 (dd, 1H, J=1.5, 10.5Hz), 3.87-3.92 (m, 3H), 6.74 (d, 1 H, J=8.5Hz), 6.84-6.96 (m, 4H), 7.00 (d, 1 H, J=7.9Hz); MS (ESI+) : 535 ([MH-Na]+).

Example 187 Preparation of 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5(S)-hydroxy-hexanoic acid

O OH ' ' OH (1 ) Preparation of 4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pen tyl]- 3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenol

OH ' i OTBS Using the same procedure as described for the preparation of Example 186- (1 ), the title compound was prepared from 4-{1-Ethyl-1-[4-(3-hydroxy-4 ,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 19). 1H-NMR: 0.07 (s, 3H), 0.10 (s, 3H), 0.60 (t, 6H), 0.88 (s, 9H), 0.93 (s, 9H), 1.51- 1.63 (m, 1 H), 1.73-1.84 (m, 1 H), 2.03 (q, 4H), 2.20 (s, 3H), 2.23 (s, 3H), 2.36- 2.46 (m, 1H), 2.71-2.81 (m, 1 H), 3.34 (dd, 1H), 4.50 (s, 1H), 6.64 (d, 1H), 6.85- 6.99 (m, 5H).

(2) Preparation of 6(S)-[4-(1 -{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxymet hyl]-tetrahydro- pyran-2-one

OTBS To a solution of 4-(1-{4-[(S)-3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl - pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenol (compound prepared in Example 187-(1)) (45.1 mg, 0.091 mmol), PPh3 (71.4 mg, 0.272 mmol) and (S)- 6-Hydroxymethyl-tetrahydro-pyran-2-one (J. Chem. Soc, Perkin Trans. 1, 2000, 20, 3519.) (35.4 mg, 0.272 mmol) in THF (0.15 ml), DEAD (47.4 mg, 0.272 mmol) was added slowly and the mixture was stirred at room temperature for 15 h. The mixture was concentrated in vacuo and purified by preparative TLC (n- hexane/ethyl acetate =3/1 ) to give the title compound (10 mg, 18.1%). 1H-NMR (chloroform-d): 0.07 (s, 3H), 0.11 (s, 3H), 0.60 (t, 6H, J=7.3Hz), 0.88 (s, 9H), 0.94 (s, 9H), 1.73-2.13 (m, 6H), 0.00 (q, 4H, J=7.3Hz), 2.36-2.81 (m, 4H)1 3.35 (dd, 1 H, J=3.3, 7.1Hz), 4.04 (dd, 1H, J=5.6, 9.8Hz), 4.13 (dd, 1H, J=4.3, 9.8Hz), 4.66-4.71 (m, 1 H), 6.67 (d, 1 H, J=8.2Hz), 6.89-6.93 (m, 4H), 6.98 (d, 1 H, J=8.5Hz).

(3) Preparation of 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5(S)-hydroxy-hexanoic acid

OTBS O OH ' ' OH O To a solution of 6(S)-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimeth yl- pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxymet hyl]-tetrahydro- pyran-2-one (compound prepared in Example 187-(2)) (10 mg, 0.016 mmol) in THF (0.2 ml), 1.0M TBAF in THF (0.4 ml, 0.4 mmol) was added and the mixture was stirred at 70 degrees C for 4 h. To the mixture, ethyl acetate was added and the mixture was washed with diluted potassium hydrogen sulfate aq., saturated sodium hydrogen carbonate solution and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The obtained residue was purified by preparative TLC (dichrolomethane/methanol =15/1) to give the title compound (3.3 mg, 39.2%). 1H-NMR (methanol^): 0.58 (t, 6H, J=7.3Hz), 0.86 (s, 9H), 1.41-1.84 (m, 6H), 2.05 (q, 4H1 J=7.3Hz), 2.14 (s, 3H), 2.28 (s, 3H), 2.35 (t, 2H, J=7.0Hz), 2.48-2.58 (m, 1 H), 2.81-2.91 (m, 1 H)1 3.15 (dd, 1 H, J=1.6, 10.6Hz), 3.87-3.93 (m, 3H), 6.74 (d, 1 H, J=8.5Hz), 6.84-6.96 (m, 4H), 7.00 (d, 1 H, J=8.0Hz); MS (ESI+) : 535 ([M+Na∏.

Example 188 Preparation of 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5(R)-hydroxy-hexanoic acid

OH (1) Preparation of 6(R)-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimeth yl- pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxymet hyl]-tetrahydro- pyran-2-one

OTBS

To a solution of 4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pen tyl]-3- methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenol (compound prepared in Example 187-(1 )) (40 mg, 0.081 mmol), PPh3 (63.3 mg, 0.242 mmol) and (R)-6- Hydroxymethyl-tetrahydro-pyran-2-one (J. Chem. Soc, Perkin Trans. 1, 2000, 20, 3519.) (31.4 mg, 0.242 mmol) in THF (0.1 ml), DEAD (42.1 mg, 0.242 mmol) was added and the mixture was stirred at room temperature for 37 h. The mixture was concentrated in vacuo and purified by preparative TLC (n- hexane/ethyl acetate =3/1 and 2/1) to give the title compound (13.5 mg, 27.4%). 1H-NMR (chloroform-d): 0.07 (s, 3H), 0.11 (s, 3H), 0.60 (t, 6H), 0.89 (s, 9H), 0.94 (s, 9H), 1.73-2.21 (m, 6H), 2.04 (q, 4H, J=7.5Hz), 2.16 (s, 3H), 2.24 (s, 3H), 2.36-2.81 (m, 4H), 3.35 (dd, 1 H, J=3.2, 7.1 Hz), 4.04 (dd, 1 H, J=5.4, 9.9Hz), 4.13 (dd, 1 H, J=4.4, 9.8Hz), 4.64-4.72 (m, 1 H), 6.67 (d, 1 H, J=8.1 Hz), 6.89-6.94 (m, 4H), 6.98 (d, 1 H, J=8.7Hz). (2) Preparation of 6-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5(R)-hydroxy-hexanoic acid

OH

To a solution of 6(R)-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimeth yl- pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxymθ thyl]-tθtrahydro- pyran-2-one (compound prepared in Example 188-(1 )) (16.5 mg, 0.033 mmol) in THF (0.2 ml) and MeOH (0.2 ml), 1 N KOH aq (0.2 ml, 0.2 mmol) was added and the mixture was stirred at 65 degrees C for 1.5 h. To the mixture, ethyl acetate was added and the mixture was washed with diluted potassium hydrogen sulfate aq., water, saturated sodium hydrogen carbonate solution and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The obtained residue was purified by preparative TLC (dichrolomethane/methanol =10/1 ) to give the title compound (8.4 mg, 49.1 %). 1H-NMR (methanol-d4): 0.57 (t, 6H, J=7.3Hz), 0.86 (s, 9H), 1.40-1.90 (m, 6H), 2.04 (q, 4H, J=7.3Hz), 2.13 (s, 3H), 2.23 (s, 3H), 2.36 (brt, 2H), 2.47-2.58 (m, 1 H), 2.81-2.91 (m, 1 H), 3.15 (dd, 1 H, J=1.5, 10.4Hz), 3.86-3.98 (m, 3H), 6.73 (d, 1 H, J=8.4Hz), 6.84-6.96 (m, 4H), 7.00 (d, 1 H, J=8.1 Hz); MS (ESI+) : 530 ([M+NH4]+).

Example 189 Preparation of 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5(R)-hydroxy-hexanoic acid

o OH i ' OH (1) Preparation of 6(R)-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimeth yl- pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxymet hyl]-tetrahydro- pyran-2-one OTBS

To a solution of 4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pen tyl]-3- methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenol (compound prepared in Example 186-(1)) (40 mg, 0.081 mmol) PPh3 (63 mg, 0.242 mmol), (R)-6-Hydroxymethyl- tetrahydro-pyran-2-one (J. Chem. Soc, Perkin Trans. 1, 2000, 20, 3519.) (31 mg, 0.242 mmol) in THF (0.1 ml), DEAD (42 mg, 0.242 mmol) was added and the mixture was stirred at room temperature for 37 h. The mixture was concentrated in vacuo and purified by preparative TLC (n-hexane/ethyl acetate =3/1 and 2/1 ) to give the title compound (13.5 mg, 27.5%). 1H-NMR (chloroform-d): 0.07 (s, 3H), 0.10 (s, 3H), 0.60 (t, 6H), 0.88 (s, 9H), 0.94 (s, 9H), 1.73-2.16 (m, 6H), 2.04 (q, 4H, J=7.5Hz), 2.16 (s, 3H), 2.24 (s, 3H), 2.36-2.81 (m, 4H), 3.35 (dd, 1 H, J=3.3, 7.1 Hz), 4.04 (dd, 1 H1 J=5.6, 9.8Hz), 4.13 (dd, 1 H, J=4.3, 9.9Hz), 4.64-4.72 (m, 1H), 6.67 (d, 1H, J=8.2Hz), 6.89-6.94 (m, 4H), 6.98 (d, 1 H, J=8.5Hz).

(2) Preparation of 6-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5(R)-hydroxy-hexanoic acid

To a solution of 6(R)-[4-(1-{4-[(R)-3-(tert-Butyl-dimethyl-silanyloxy)-4,4-di methyl- pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxymet hyl]-tetrahydro- pyran-2-one (compound prepared in Example 189-(1 )) (16.5 mg, 0.027 mmol) in THF (0.2 ml) and MeOH (0.2 ml), 1 N KOH aq (0.2 ml, 0.2 mmol) was added at room temperature and the mixture was stirred at 65 degrees C for 1.5 h. To the mixture, ethyl acetate was added and the mixture was washed with diluted potassium hydrogen sulfate aq., water, saturated sodium hydrogen carbonate solution and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The obtained residue was purified by preparative TLC (dichrolomethane/methanol =10/1 , twice) to give the title compound (6.9 mg, 49.7%). 1H-NMR (methanol-d4): 0.58 (t, 6H, J=7.3Hz), 0.86 (s, 9H), 1.38-1.84 (m, 6H), 2.05 (q, 4H, J=7.3Hz), 2.14 (s, 3H), 2.23 (s, 3H), 2.34 (t, 2H, J=7.0Hz), 2.47-2.58 (m, 1 H), 2.81-2.91 (m, 1 H), 3.15 (dd, 1 H, J=1.5, 10.5Hz), 3.87-3.98 (m, 3H), 6.73 (d, 1 H, J=8.6Hz), 6.84-6.96 (m, 4H), 7.00 (d, 1 H, J=7.9Hz); MS (ESI+) : 513 ([M+H]+).

Example 190 Preparation of 6(R)-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-o ne

Preparation of 6(R)-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-tetrahydro-pyran-2-o ne

To a solution of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl - phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(5)) (30 mg, 0.079 mmol), PPh3 (62.0 mg, 0.236 mmol), (R)-6-Hydroxymethyl-tetrahydro- pyran-2-one (J. Chem. Soc, Perkin Trans. 1, 2000, 20, 3519.) (30.8 mg, 0.236 mmol) in THF (0.1 ml), DEAD (41.2 mg, 0.236 mmol) was added slowly and the mixture was stirred at room temperature for 37 h. The mixture was concentrated in vacuo and purified by preparative TLC (n-hexane/ethyl acetate =1/3, 3/1 , 3 times, 1/1 , dichloromethane/methanol=15/1) to give the title compound (8.5 mg, 21.9%). 1H-NMR (chloroform-d): 0.61 (t, 6H, J=7.3Hz), 0.92 (t, 6H, J=7.5Hz), 1.64 (q, 4H, J=7.6Hz), 1.82-1.95 (m, 4H), 2.05 (q, 4H, J=7.3Hz), 2.16 (s, 3H), 2.31 (s, 3H), 2.46-2.71 (m, 2H), 4.04 (dd, 1 H, J=5.5, 9.9Hz), 4.13 (dd, 1 H, J=4.3, 9.9Hz), 4.65-4.72 (m, 1 H), 6.01 (d, 1 H, J=16.1 Hz), 6.67 (d, 1 H1 J=8.5Hz), 6.74 (d, 1 H1 J=16.0Hz), 6.92-6.97 (m, 4H), 7.29 (d, 1 H, J=8.6Hz); MS (ESI+) : 510 ([M+NH4]+).

Example 191 Preparation of 6-(4-{1 -Ethyl- 1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5(R)-hydroxy-hexanoic acid

o OH Preparation of 6-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-5(R)-hydroxy-hexanoic acid

To a solution of 6(R)-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-tetrahydro-py ran-2-one (compound prepared in Example 190) (5.9 mg, 0.012 mmol) in THF (0.1 ml) and , MeOH (0.1 ml), 1 N KOH aq (0.1 ml, 0.1 mmol) was added at room temperature and the mixture was stirred at 70 degrees C for 4 h. To the mixture, ethyl acetate was added and the mixture was washed with diluted potassium hydrogen sulfate aq. and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The obtained residue was purified by preparative TLC (dichrolomethane /methanol =15/1 , twice) to give the title compound (4.9mg, 80.1%). 1H-NMR (methanol-d4): 0.59 (t, 6H, J=8.1 Hz), 0.91 (t, 6H, J=8.3Hz), 1.62 (q, 4H, J=8.3Hz), 1.52-1.82 (m, 4H), 2.06 (q, 4H, J=8.1Hz), 2.14 (s, 3H), 2.21 (t, 2H, J=8.0Hz), 2.27 (s, 3H), 3.82-3.98 (m, 3H), 5.98 (d, 1 H, J=17.8Hz), 6.75 (d, 1 H, J=17.9Hz), 6.75 (d, 1 H, J=9.3Hz), 6.91-6.96 (m, 3H), 7.27 (d, 1 H, J=9.2Hz); MS (ESI+) : 493 ([M-OH]+).

Example 192 Preparation of 6-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-i-ynyO-phenyll-propylJ^-methyl-phenyO-he x-δ-ynoic acid

HOOC

(1 ) Preparation of Trifluoro-methanesulfonic acid 4-{1 -ethyl-1 -[3-methyl-4-(4,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenyl ester

TfO

o— To a solution of 4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-methoxymethoxy-3- trifluoromethyl-but-1 -ynyl)-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 2-(2)) (200 mg, 0.398 mmol) in CH2CI2 (2 ml), pyridine (63.8 mg, 0.796 mmol) and trifluoromethanesulfonic anhydride (0.0737 ml, 0.438 mmol) were added and the mixture was stirred at room temperature for 16h. The mixture was chromatographed on silica gel (ethyl acetate/n- hexane = 0/100 to 1/5) to give the title compound (197 mg, 78%). 1H-NMR: 0.60 (t, 6H), 2.06 (q, 4H), 2.32 (s, 3H), 2.41 (s, 3H), 3.48 (s, 3H), 5.15 (s, 2H), 6.94-7.05 (m, 4H), 7.12 (d, 1 H), 7.30 (d, 1 H).

(2) Preparation of Hex-5-ynoic acid methyl ester To a solution of hex-5-ynoic acid (2.0 g, 17.9 mmol) in MeOH (4 ml), cone. H2SO4 (4 drops) was added at room temperature and the mixture was stirred at 60 degrees C for 60 h. To the mixture, ethyl acetate was added and the mixture was washed with saturated NaHCO3, dried over MgSO4 filtered and concentrated in vacuo to give the title compound (2.0 g, 89%). 1H-NMR: 1.80-1.90 (m ,2H), 1.97-1.99 (m, 1 H), 2.23-2.30 (m, 2H), 2.48 (t, 2H), 3.68 (s, 3H)

(3) Preparation of 6-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-methoxymethoxy- S-trifluoromethyl-but-i-ynyO-phenylJ-propylJ^-methyl-phenyO- hex-δ-ynoic acid methyl ester

TfO

To a solution of trifluoro-methanesulfonic acid 4-{1-ethyl-1-[3-methyl-4-(4,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1 -ynyl)-phenyl]-propyl}-2- methyl-phenyl ester (compound prepared in Example 192-(1 )) (23 mg, 0.0363 mmol) in DMF (0.5 ml), Et3N (0.0253 ml, 0.182 mmol), CuI (3.4 mg, 0.0181 mmol), PdCI2(PPh3)2 (12.7 mg, 0.0181 mmol) and hex-5-ynoic acid methyl ester (compound prepared in Example 192-(2)) (13.7 mg, 0.109 mmol) were added at room temperature and the mixture was stirred at 160 degrees C for 30min. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was purified by preparative TLC (n-hexane:ethyl acetate=5:1 ) to give the title compound (8.5 mg, 38%). 1H-NMR: 0.59 (t, 6H), 1.91 (t, 2H), 2.08 (q, 4H), 2.34 (s, 3H), 2.39 (s, 3H), 2.53 (t, 2H), 3.48 (s, 2H), 3.68 (s, 3H), 5.15 (s, 2H), 6.87-7.38 (m, 6H). (4) Preparation of 6-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-i-ynyO-phenylJ-propylJ^-methyl-phenyO-he x-δ-ynoic acid methyl ester

MeOOC

6-(4-{1-ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-methoxymet hoxy-3-trifluoromethyl- but-1-ynyl)-phenyl]-propyl}-2-methyl-phenyl)-hex-5-ynoic acid methyl ester (compound prepared in Example 192-(3)) (8.5 mg, 0.0139 mmol) was dissolved in 4N HCI/dioxane (0.5 ml) at room temperature, and the mixture was stirred at room temperature for 16 h. The mixture was concentrated in vacuo and purified by preparative TLC (n-hexane:ethyl acetate=5:1) to give the title compound (6.3 mg, 80%). 1H-NMR: 0.60 (t, 6H), 1.92 (t, 2H), 2.04 (q, 4H), 2.35 (s, 3H), 2.37 (s, 3H), 2.52 (t, 2H), 3.70 (s, 3H), 6.83-7.39 (m, 6H); MS (ESI+) : 584 ([M+NH4∏.

(5) Preparation of 6-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenyl) -hex-5-ynoic acid

MeOOC HOOC

To a solution of 6-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenyl) -hex-5-ynoic acid methyl ester (compound prepared in Example 192-(4)) (6.3 mg, 0.0111 mmol) in MeOH (0.5 ml), 1N NaOH (0.1 ml) was added and the mixture was stirred at room temperature for 1h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (2.4mg, 39%). 1H-NMR: 0.61 (t, 6H)1 1.90-1.99 (m, 2H), 2.06 (q, 4H), 2.35 (s, 3H)1 2.37 (s, 3H), 2.52-2.60 (m, 2H), 6.85-7.02 (m, 4H), 7.35 (d, 1 H); MS (ESI+) : 570 ([M+NH4]+).

Example 193 Preparation of 7-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenyl) -hept-6-ynoic acid

HOOC

(1) Preparation of Hept-6-ynoic acid methyl ester

#^^^COOH ^^^^^COOMe To a solution of hept-6-ynoic acid (2.0 g, 15.9 mmol) in MeOH (4 ml), cone. H2SO4 (4 drops) was added at room temperature and stirred at 60 degrees C for 60 h. To the mixture, ethyl acetate was added and the mixture was washed with saturated NaHCO3, dried over MgSO4 and concentrated in vacuo to give the title compound (2.0 g, 90%). 1H-NMR: 1.52-1.61 (m, 2H), 1.68-1.80 (m, 2H), 1.95-1.97 (m, 1 H), 2.18-2.23 (m, 2H), 2.35 (t, 2H), 3.68 (s, 3H).

(2) Preparation of 7-(4-{1-Ethyl-1-[3-methyl-4-(4 ,4,4-trifluoro-3-methoxymethoxy- 3-trifluoromethyl-but-1 -ynyl)-phenyl]- propyl}-2-methyl-phenyl)-hept-6-ynoic acid methyl ester

TfO 0^x MeOOC CF3 o- To a solution of trifluoro-methanesulfonic acid 4-{1 -ethyl-1 -[3-methyl-4-(4 ,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-propyl}-2- methyl-phenyl ester (compound prepared in Example 192-(1)) (23 mg, 0.0363 mmol) in DMF (0.5 ml), Et3N (0.0253 ml, 0.182 mmol), CuI (3.4 mg, 0.0181 mmol), PdCI2(PPh3)2 (12.7 mg, 0.0181 mmol) and hept-6-ynoic acid methyl ester (15.3 mg, 0.109 mmol) were added at room temperature and the mixture was stirred at 160 degrees C for 30min. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, concentrated in vacuo and purified by preparative TLC (n-hexane:ethyl acetate=5:1) to give the title compound (4.0 mg, 18%). 1H-NMR: 0.59 (t, 6H), 2.08 (q, 4H), 2.35 (s, 3H), 2.38 (s, 3H), 2.47 (t, 2H), 3.47 (s, 2H)1 3.67 (s, 3H), 5.15 (s, 2H), 6.87-7.38 (m, 6H).

(3) Preparation of 7-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenyl) -hept-6-ynoic acid methyl ester

MeOOC

MeOOC

7-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-bu t-1 - ynyl)-phenyl]-propyl}-2-methyl-phenyl)-hept-6-ynoic acid methyl ester (compound prepared in Example 193-(2)) (4.0 mg, 0.0064 mmol) was dissolved in 4N HCI/dioxane (0.5 ml) at room temperature, the mixture was stirred at room temperature for 16 h. The mixture was concentrated in vacuo and purified by preparative TLC (n-hexane:ethyl acetate=5:1) to give the title compound (2.6 mg, 70%). 1H-NMR: 0.60 (t, 6H), 1.85-1.91 (m, 2H), 2.05 (q, 4H), 2.35 (s, 3H), 2.37 (s, 3H), 2.47 (t, 2H), 3.67 (s, 3H), 6.83-7.37 (m, 6H); MS (ESI+) : 598 ([M+NH4]+).

(4) Preparation of 7-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1 -ynyl)-phenyl]-propyl}-2-methyl-phenyl)-hept-6-ynoic acid MeOOC

To a solution of 7-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-i-ynyO-phenyll-propylJ^-methyl-phenyO-he pt-δ-ynoic acid methyl ester (2.6 mg, 0.0045 mmol) in MeOH (0.5 ml), 1 N NaOH (0.1 ml) was added and the mixture was stirred at room temperature for 1h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCl3:MeOH=8:3 saturated with H2O) to give the title compound (1.0 mg, 40%). 1H-NMR: 0.59 (t, 6H), 1.79-1.89 (m, 2H), 2.06 (q, 4H), 2.35 (s, 3H), 2.37 (s, 3H), 2.42-2.50 (m, 2H), 6.85-7.35 (m, 6H); MS (ESI+) : 584 ([M+NH4∏.

Example 194 Preparation of 5-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2- methyl-phenoxymethyl)- furan-2-carboxylic acid

HOOC-/ J O OH (1) Preparation of 5-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pentyl]-3-methyl-phenyl} -1-ethyl-propyl)-2-methyl-phenoxymethyl]-furan-2- carboxylic acid ethyl ester

EtOOC OTBS OTBS To a solution of 4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pen tyl]-3- methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenol (compound prepared in Example 187-(1 )) (60 mg, 0.12 mmol) in DMF (0.6 ml), ethyl 5-(chloromethyl)-2-furan carboxylatθ (27 mg, 0.14 mmol), and K2CO3 (20 mg, 0.14 mmol) were added at room temperature and stirred at 80 degrees C for 8 h. To the mixture, ethyl acetate was added and the mixture was washed with saturated NH4CI solution and water, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (ethyl acetate/hexane =1/4) to give the title compound (60 mg, 93%) as colorless oil. 1H-NMR (CDCI3): 0.06 (s, 3H),0.1 (s, 3H),0.6 (t, 6H , J=7.3Hz),0.88 (s, 9H),0.93 (s, 9H),1.38 (t, 3H , J=7.2Hz),1.52-1.64 (m, 1H),1.71-1.82 (m, 1H),2.04 (q, 4H , J=7.3Hz),2.17 (s, 3H),2.23 (s, 3H),2.41 (dt, 1H , J=4.7, 13.2Hz),2.76 (dt, 1 H , J=5.4, 12.8Hz),3.34 (dd, 1 H , J=3.3, 7.3Hz),4.37 (q, 2H , J=7.2Hz),6.49 (d, 1 H , J=3.5Hz),6.73 (d, 1H , J=9.1Hz),6.9-7.0 (m, 5H),7.15 (d, 1H , J=3.5Hz).

(2) Preparation of 5-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl -phenoxymethyl)-furan-2-carboxylic acid

B00C" \J) i i ότBs VJ i i OH To a solution of 5-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pentyl]- S-methyl-phenylJ-i-ethyl-propyO^-methyl-phenoxymethyll-furan ^-carboxylic acid ethyl ester (compound prepared in Example 194-(1)) (60 mg, 0.11 mmol) in THF (1 ml), TBAF (1.0 M in THF) (1 ml, 1 mmol) was added at room temperature and refluxed for 5 h. To the mixture, ethyl acetate was added and the mixture was washed with 30% NaHaPO4 aq. and brine, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (MeOH/CH2CI2 =1/10) to give the title compound (25 mg, 45%) as colorless oil. 1H-NMR (CDCI3): 0.59 (t, 6H , J=7.3Hz),0.89 (s, 9H),1.43-1.58 (m, 1H),1.74-1.82 (m, 1H),2.03 (q, 4H, J=7.3Hz),2.16 (s, 3H),2.25 (s, 3H),2.5-2.61 (m, 1H),2.81- 2.92 (m, 1H),3.25 (dd, 1H, J=1.6, 10.4Hz),4.06 (brs, 1H),5.04 (s, 2H),6.5-6.49 (d, 1H1 J=3.5Hz),6.73-6.70 (d, 1 H, J=5.5Hz),6.89-6.95 (m, 4H),7.02 (d, 1 H, J=8.6Hz),7.25 (d, 1 H, J=4.3Hz); MS (ESI+) : 529 ([M+Na∏. Example 195 Preparation of Preparation of (E)-N-(2-Amino-ethyl)-2-(4-{1-ethyl-1-[4-(3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheno xy)-acetamide

H H2N'^S^N^>SO O (1) Preparation of (E)-{2-[2-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3 - methyl-phenyl]-propyl}-2-methyl-phenoxy)-acetylamino]-ethyl} -carbamic acid 9H- fluoren-9-ylmethyl ester

HO2C FmocHN ^^N

To a solution of (4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-acetic acid (compound prepared in Example 151 -(2)) (74.4 mg, 0.17 mmol) in CH2CI2 (1.7 ml) and diisopropylethylamine (0.118ml, 0.68 mmol) was added (2-Amino-ethyl)-carbamic acid 9H-fluoren-9- ylmethyl ester (108 mg, 0.34 mmol), WSCI hydrochloride (65 mg, 0.34 mmol) and HOBt monohydrate (26 mg, 0.17 mmol), and the mixture was stirred for 18 h at room temperature. The reaction mixture was poured into H2O and extracted with CH2CI2. The organic phase was concentrated in vacuo. The resulting residue was chromatographed on silica gel (ethyl acetate/hexane = 60/40 to 100/0) to give the title compound (92.2 mg, 77%). 1H-NMR: 0.59 (t, 6H), 0.91 (t, 6H), 1.63 (dq, 4H), 2.03 (q, 4H), 2.21 (s, 3H), 2.30 (s, 3H), 3.30-3.55 (m, 4H), 4.19 (t, 1 H), 4.38 (d, 2H), 4.47 (s, 2H), 5.16 (br, 1 H), 6.00 (d, 1 H), 6.62 (d, 1 H), 6.73 (d, 1 H), 6.90-7.75 (m, 14H).

(2) Preparation of (E)-N-(2-Amino-ethyl)-2-(4-{1 -ethyl-1 -[4-(3-ethyl-3-hydroxy- pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-acet amide -\^N FmocHN -► O To a solution of {2-[2-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3-met hyl- phenyl]-propyl}-2-methyl-phenoxy)-acetylannino]-ethyl}-carba nnic acid 9H-fluoren- 9-ylmethyl ester (92 mg, 0.13 mmol) in DMF (1.3 ml), diethylamine (0.134 ml, 1.3 mmol) was added and the mixture was stirred for 3 h at room temperature. The reaction mixture was poured into water and the products were extracted with AcOEt. The extracts were washed with H2O twice, dried over MgSO4, filtered and concentrated in vacuo. The obtained residue was chromatographed on silica gel (ethyl acetate/EtOH = 10/1) to give the title compound (41.1 mg, 65%). 1H-NMR: 0.61 (t, 6H), 0.92 (t, 6H), 1.64 (dq, 4H), 2.05 (q, 4H), 2.23 (s, 3H), 2.31 (s, 3H), 2.87 (t, 2H), 3.40 (q, 2H), 4.49 (s, 2H), 6.01 (d, 1 H), 6.66 (d, 1 H), 6.74 (d, 1 H), 6.90-7.75 (m, 6H).

Example 196 Preparation of Preparation of (E)-2-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1- enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-N-(2-hydrox y-ethyl)-acetamide

H

H O Preparation of (E)-2-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-N-(2-hydroxy-ethyl)-acetam ide

H HO2C HO^N^O H O To a solution of (4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-acetic acid (compound prepared in Example 151 -(2)) (78 mg, 0.178 mmol) in CH2CI2 (1.8 ml) and triethylamine (0.074 ml, 0.534 mmol) was added ethanolamine (0.032 ml, 0.534 mmol), WSCI hydrochloride (102 mg, 0.534 mmol) and HOBt monohydrate (27 mg, 0.178 mmol), and the mixture was stirred for 2 h at room temperature. To the reaction mixture, H2O was added and separated. The organic phase was concentrated in vacuo. The resulting residue was chromatographed on silica gel (ethyl acetate/hexane = 60/40 to 100/0) to give the title compound (21.5 mg, 25%). 1H-NMR: 0.61 (t, 6H)1 0.92 (t, 6H), 1.64 (dq, 4H), 2.05 (q, 4H), 2.22 (s, 3H), 2.31 (s, 3H), 3.54 (q, 2H) , 3.76-3.79 (m, 2H), 4.50 (s, 2H), 6.01 (d, 1 H), 6.65-7.31 (m, 8H); MS (ESI+) : 464 ([M-OH]+).

Example 197 Preparation of [2-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl-phenyl]-propyl}- 2-methyl-phenoxy)-acetylamino]-acetic acid

HO2C^ HN^QA Il Q i i ΓOH

Preparation of [2-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-acetylamino]-acetic acid

H HO2C>

To a solution of (4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-acetic acid (compound prepared in Example 151 -(2)) ( (172 mg, 0.39 mmol) in CH2CI2 (3.9 ml) and triethylamine (0.231 ml, 1.66 mmol) was added H-GIy-OMe hydrochloride (98 mg, 0.78 mmol), WSCI hydrochloride (150 mg, 0.78 mmol) and HOBt monohydrate (60 mg, 0.39 mmol), stirred for 18 h at room temperature. The reaction mixture was concentrated in vacuo, separated with ethyl acetate and aqueous KHSO4, the organic phase was washed with aqueous NaHCO3 and brine, dried over MgSO4, concentrated in vacuo to obtain the residue (174 mg). Then, 96.8 mg of the residue was dissolved with THF (1 ml) and MeOH (1 ml), 1 N aqueous KOH (1 ml) was added and the mixture was stirred for 1 h at room temperature. The reaction mixture was concentrated in vacuo, separated with ethyl acetate and aqueous KHSO4, the organic phase was washed with brine, dried over MgSO4, concentrated in vacuo, and chromatographed on silica gel (MeOH/CHCU = 0/100 to 27/73) to give the title compound (87 mg, 81 %). 1H-NMR (CD3OD): 0.59 (t, 6H), 0.91 (t, 6H), 1.62 (q, 4H), 2.06 (q, 4H), 2.22 (s, 3H), 2.26 (s, 3H), 3.84 (s, 2H), 4.49 (s, 2H), 5.98 (d, 1 H), 6.71-6.99 (m, 6H) 7.27 (d, 1 H).; MS (El): 477 ([M-H2O]+).

Example 198 Preparation of (E)-5-(4-{1 -Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4-oxo-pentanoic acid

HO5C H

(1 ) Preparation of (E)-5-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-oxo-pentanoic acid methyl ester

To a solution of 5-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan-2-one (compound prepared in Example 44) (194 mg, 0.41 mmol) was dissolved with THF (1.5 ml) and MeOH (1.5 ml). 1 N aqueous KOH (1.5 ml) was added and the mixture was stirred for 1 h at room temperature. The reaction mixture was concentrated in vacuo, separated with ethyl acetate and aqueous KHSO4, the organic phase was washed with brine, dried over MgSO4, concentrated in vacuo. The resulting residue was dissolved with CH2CI2 (0.8 ml), tetrapropylammmonium perruthenate (14.4 mg, 0.041 mmol), MS4A (200 mg), and N-methylmorphorine- N-oxide (96 mg, 0.82 mmol) was added and stirred for 2 h at room temperature. The reaction mixture was concentrated in vacuo and treated with short pad of silica gel (ethyl acetate/EtOH = 10/1). The resulting black residue was dissolved with Et2O (2 ml) and MeOH (1 ml). Trimethylsilyldiazomethane (2M in hexane, ca.0.2 ml), was added and stirred for 2 min. at room temperature. The reaction mixture was concentrated in vacuo and chromatographed (ethyl acetate / hexane = 15/85 to 30/70) to give the title compound (65 mg, 32%). 1H-NMR : 0.61 (t, 6H), 0.91 (t, 6H), 1.64 (q, 4H), 2.05 (q, 4H), 2.24 (s, 3H), 2.31 (s, 3H), 2.66 (t, 2H), 2.99 (t, 2H), 3.68 (s, 3H), 4.55 (s, 2H), 6.01 (d, 1 H), 6.56 (d, 1 H), 6.74 (d, 1H), 6.92-6.96 (m, 4H), 7.30 (d, 1H).

(2) Preparation of (E)-5-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-oxo-pentanoic acid

o

To a solution of 5-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4-oxo-pentanoic acid methyl ester (compound prepared in Example 198-(1 )) (65 mg, 0.41 mmol) was dissolved with THF (1 ml) and MeOH (1 ml). 1 N aqueous KOH (1 ml) was added and the mixture was stirred for 1 h at room temperature. The reaction mixture was concentrated in vacuo, separated with ethyl acetate and aqueous KHSO4, the organic phase was washed with brine, dried over MgSO4, concentrated in vacuo to give the title compound (63 mg, 100%). 1H-NMR(CD3OD): 0.61 (t, 6H), 0.91 (t, 6H), 1.62 (q, 4H), 2.06 (q, 4H), 2.19 (s, 3H), 2.26 (s, 3H), 2.59-2.63 (m, 2H), 2.84-2.88 (m, 2H), 5.98 (dd, 1 H), 6.64 (d, 1 H), 6.74 (d, 1 H), 6.89-6.95 (m, 4H), 7.27 (d, 1 H),.; MS (El): 476 ([M-H2O] +).

Example 199 Preparation of (E)-3-[2-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenylj-propylj^-methyl-phenoxyj-acetylaminoj-propionic acid H HO2C"^N^O H O Preparation of (E)-3-[2-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-acetylamino]-propionic acid

H HO5C^O HO5 "V H

To a solution of (4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-acetic acid (compound prepared in Example 151 -(2)) ( (166 mg, 0.38 mmol) in CH2CI2 (3.8 ml) and triethylamine (0.212 ml, 1.52 mmol) was added H-beta-Ala-OMe hydrochloride (106 mg, 0.76 mmol), WSCI hydrochloride (146 mg, 0.76 mmol) and HOBt monohydrate (58 mg, 0.38 mmol), and the mixture was stirred for 18 h at room temperature. The reaction mixture was concentrated in vacuo, separated with ethyl acetate and aqueous KHSO4, the organic phase was washed with aqueous NaHCO3 and brine, dried over MgSO4, concentrated in vacuo to obtain the residue (162mg). Then, 103.6 mg of the residue was dissolved with THF (1 ml_) and MeOH (1 ml). 1N aqueous KOH (1 ml) was added and the mixture was stirred for 1 h at room temperature. The reaction mixture was concentrated in vacuo, separated with ethyl acetate and aqueous KHSO4, the organic phase was washed with brine, dried over MgSO4, concentrated in vacuo, and chromatographed on silica gel (MeOH/CHCI3= 0/100 to 27/73) to give the title compound (78 mg, 63%). 1H-NMR: 0.60 (t, 6H), 0.91 (t, 6H), 1.63 (dq, 4H), 2.04 (q, 4H), 2.20 (s, 3H), 2.30 (s, 3H), 2.64 (t, 2H), 3.64 (q, 2H), 4.45 (s, 2H), 6.00 (d, 1 H), 6.63 (d, 1H), 6.73 (d, 1 H), 6.91-7.30 (m, 5H).; MS (El) : 491 ([M-H2O]+).

Example 200 Preparation of (2S,3S)-2-[2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4 ,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-acetylamino]-3-meth yl-pentanoic acid (1) Preparation of [4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pe ntyl]- 3-methyl-phenyl}-1-ethyl-propyl) -2-methyl-phenoxy]-acetic acid methyl ester

MeO OTBS O ' ' OTBS To a solution of compound prepared in Example 186-(1) (4-(1-{4-[3-(tert-Butyl- dimethyl-silanyloxy)-4,4-dimethyl-pentyl]-3-methyl-phenyl}-1 -ethyl-propyl)-2- methyl-phenol) (450 mg, 0.91 mmol) in acetone (10 ml), K2CO3 (377 mg, 2.73 mmol) and bromoacetic acid methyl ester (278 mg, 1.82 mg) were added at room temperature and the mixture was stirred at 45 degrees C for 68 h. The mixture was applied onto silica and chromatographed (n-hexane only to n- hexane:ethyl acetate=5:1) to give the title compound (436 mg, 84%). 1H-NMR: 0.07 (s, 3H), 0.11 (s, 3H), 0.60 (t, 6H), 0.89 (s, 9H), 0.94 (s, 9H), 2.03 (s, 4H), 2.24 (s, 6H), 2.35-2.46 (m, 1 H), 2.70-2.82 (m, 1 H), 3.33-3.38 (m, 1 H), 3.80 (s, 3H), 4.62 (s, 2H), 6.59 (d, 1H), 6.88-7.00 (m, 5H).

(2) Preparation of [4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pe ntyl]- 3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxy]-acetic acid

MeO OTBS OTBS To a solution of [4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pe ntyl]- 3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxy]-acetic acid methyl ester (436 mg, 0.767 mmol) in EtOH (3 ml), 1N NaOH (1 ml) was added at room temperature and the mixture was stirred at room temperature for 16 h. To the mixture, 1 % HCI was added to adjust pH at 6 and extracted with ethyl acetate, washed with brine, dried over MgSO4 and concentrated in vacuo to give the title compound (424 mg, 100%). 1H-NMR: 0.07 (s, 3H), 0.10 (s, 3H), 0.60 (t, 6H), 0.88 (s, 9H)1 0.94 (s, 9H), 2.03 (s, 4H), 2.23 (s, 6H), 2.35-2.47 (m, 1 H), 2.70-2.82 (m, 1 H), 3.33-3.38 (m, 1 H), 4.61 (s, 2H), 6.62 (d, 1 H), 6.88-7.02 (m, 5H).

(3) Preparation of (2S,3S)-2-[2-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl )- 3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-acetylamino]-3-me thyl-pentanoic acid

Fmoc-L-lle-Wang resin OTBS

O

OH

Fmoc-L-lle-Wang resin (0.57 mmol/g as amino acid loading, 35 mg, 0.020 mmol amino acid loading) was treated with 20% (v/v) piperidine in DMF (0.5 ml) two times to deprotect Fmoc group and washed with DMF (1 ml, 5 times). To the resin, solutions of [4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxy]-a cetic acid (16.0 mg, 0.029 mmol) in DMF (0.2 ml), benzotriazole-1-yl-oxy- tris(dimethylamino)phosphonium hexafluorophosphate (17.7 mg, 0.040 mmol) in DMF (0.2 ml) and N,N-diisopropyl ethyl amine (0.0105 ml, 0.060 mmol) in DMF (0.1 ml) were added at room temperature, agitated at room temperature for 16h, filtrated, washed with DMF (2 ml, 3 times), i-PrOH (2 ml, 3 times), THF (2 ml, 3 times), MeOH (2 ml, 3 times) and CH2CI2 (2 ml, 3 times) and dried in vacuo. To the resin, 20% TFA in CH2CI2 (v/v) (1 ml) was added at room temperature, agitated at room temperature for 16h, filtrated, washed with CH2CI2 (1 ml, 2 times) and concentrated in vacuo. The residue was purified by preparative

reverse phase HPLC (CAPCELLPAK C18 MG2 20mm(ID)-50mnn column,

gradient elution 50 to 90% B/A over 10min, and 100% B over 2.5min (solvent A

= 1OmM ammonium acetate H2O, solvent B = MeOH1 UV detection at 220 and

277nm) to give the titled compound (3.4 mg, 31%).

1H-NMR: 0.59 (t, 6H), 0.89 (s, 9H), 0.89-0.97 (m, 6H)1 2.04 (q, 4H), 2.23 (s, 3H),

2,25 (s, 3H), 3.25 (d, 1 H), 4.51 (s, 2H), 4.60-4.68 (m, 1 H), 5.30 (s, 2H), 6.65 (d,

1 H), 6.88-7.05 (m, 4H), 7.12 (d, 1 H); MS (ESI+) : 571 ([M+NH4]+).

Example 201-202

Examples 201 to 202 were prepared according to same procedure as Example

200-(3) from corresponding Fmoc-amino acid-Wang resin listed in below table.

Example 1H-NMR in yield yield compound structure MS # CD3OD (mg) (%) 2(S)-[2-(4-{1- Ethyl-1-[4-(3- hydroxy-4,4- 0.58 (t, 6H), 0.89 dimethyl- (t, 9H), 2.04 (q, pentyl)-3- O^ J O I ' OH 4H), 2.25 (s, 6H), 573 201 methyl-pnenyl]- OH 3.15 (d, 1H), 4.50 1.7 15 ([M+NH4]+) propyI}-2- (S, 2H), 4.63 (t, methyl- 1H), 6.72 (d, 1 H), phenoxy)- 6.87-7.04 (m, H) acetylamino]- succinic acid 3-[2-(4-{1-Ethyl- 0.59 (t, 6H), 0.89 1-[4-(3-hydroxy- (s, 9H), 2.03 (q, 4,4-dimethyl- 4H), 2.20 (s, 3H), pentyl)-3- 0 o I ' OH 2.25 (s, 3H), 2.61 methyl-phenyl]- 529 202 (t, 2H), 3.22 (d, 3.7 36 propyl}-2- ([MH-NH4]*) 1H), 3.62 (q, 2H), methyl- 4.46 (S, 2H), 6.71 phenoxy)- (d, 1H), 6.87-7.04 acetylamino]- (m, 5H) propionic acid

Starting Fmoc-amino acid-Wang resin

amino acid loading on reacted resin Example # Fmoc-amino acid-Wang resin resin (mg) (mmol/g) 201 Fmoc-L-Asp(OtBu)-Wang resin 0.59 33.9 202 Fmoc-beta-Ala-Wang resin 0.52 38.5

Example 203 Preparation of [2-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-acetylamino]-acetic acid

OH Preparation of [4-(1 -{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pentyl] -3- methyl-phenyl}-1 -ethyl-propyl) -2-methyl-phenoxy]-acetic acid methyl ester

MeO OTBS OTBS To a solution of compound prepared in Example 187-(1 ) (4-(1-{4-[3-(tert-Butyl- dimethyl-silanyloxy)-4,4-dimethyl-pentyl]-3-methyl-phenyl}-1 -ethyl-propyl)-2- methyl-phenol) (1.00 g, 2.02 mmol) in acetone (20 ml), K2CO3 (836 mg, 6.06 mmol) and bromoacetic acid methyl ester (618 mg, 4.04 mmol) was added at room temperature and stirred at 45 degrees C for 68 h. The mixture was applied onto silica and chromatographed (n-hexane only to n-hexane:ethyl acetate=5:1) to give the title compound (720 mg, 63%). 1H-NMR: 0.06 (s, 3H), 0.11 (s, 3H)1 0.59 (t, 6H), 0.88 (s, 9H)1 0.93 (s, 9H), 2.03 (s, 4H), 2.23 (s, 6H), 2.35-2.46 (m, 1 H), 2.70-2.82 (m, 1H), 3.34 (dd, 1 H), 3.80 (s, 3H), 4.61 (s, 2H), 6.57 (d, 1 H), 6.90-6.99 (m, 5H).

(2) Preparation of [4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pe ntyl]- 3-methyl-phenyl}-1 -ethyl-propyl)-2-methyl-phenoxy]-acetic acid

OTBS O ' ' OTBS To a solution of [4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pe ntyl]- 3-methyl-phenyl}-1-ethyl-propyl) -2-methyl-phenoxy]-acetic acid methyl ester prepared in Example 203-(1 ) (720 mg, 1.27 mmol) in MeOH (5 ml) and THF (5 ml), 1 N NaOH (1 ml) was added at room temperature and the mixture was stirred at room temperature for 16h. To the mixture, 1% HCI was added to adjust pH at 6 and extracted with ethyl acetate, washed with brine, dried over MgSO4 and concentrated in vacuo to give the title compound (690 mg, 100%). 1H-NMR: 0.07 (s, 3H), 0.10 (s, 3H), 0.60 (t, 6H), 0.88 (s, 9H), 0.93 (s, 9H), 2.05 (s, 4H), 2.23 (s, 6H), 2.35-2.46 (m, 1 H), 2.70-2.82 (m, 1 H), 3.34 (dd, 1 H), 4.65 (s, 2H), 6.61 (d, 1 H), 6.88-7.02 (m, 5H).

(3) Preparation of [2-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl - phenyl]-propyl}-2-methyl-phenoxy)-acetylamino]-acetic acid

Fmoc-Gly-Wang resin OTBS

O

OH Fmoc-Gly-Wang resin (0.73 mmol/g as amino acid loading, 27.4 mg, 0.020 mmol amino acid loading) was treated with 20% (v/v) piperidine in DMF (0.5 ml) two times to deprotect Fmoc group and washed with DMF (1 ml, 5 times). To the resin, solutions of [4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pe ntyl]- 3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxy]-acetic acid (16.0 mg, 0.029 mmol) in DMF (0.2 ml), benzotriazole-1-yl-oxy-tris(dimethylamino)phosphonium hexafluorophosphate (17.7 mg, 0.040 mmol) in DMF (0.2 ml) and N1N- diisopropyl ethyl amine (0.0105 ml, 0.060 mmol) in DMF (0.1 ml) were added at room temperature, agitated at room temperature for 16h, filtrated, washed with DMF (2 ml, 3 times), i-PrOH (2 ml, 3 times), THF (2 ml, 3 times), MeOH (2 ml, 3 times) and CH2CI2 (2 ml, 3 times) and dried in vacuo. To the resin, 20% TFA in CH2CI2 (v/v) (1 ml) was added at room temperature, agitated at room temperature for 16 h, filtrated, washed with CH2CI2 (1 ml, 2 times) and concentrated in vacuo. The residue was purified by preparative reverse phase HPLC (CAPCELLPAK C18 MG2 20mm(ID)-50mm column, gradient elution 50 to 90% B/A over 10min, and 100% B over 2.5min (solvent A = 1OmM ammonium acetate H2O, solvent B = MeOH, UV detection at 220 and 277nm) to give the titled compound (2.6 mg, 26%). 1H-NMR: 0.59 (s, 6H), 0.87 (s, 9H), 2.07 (q, 4H), 2.24 (S, 6H), 3.15 (d, 1 H), 3.91 (d, 2H), 4.52 (s, 2H), 6.77 (d, 1H), 6.87-7.04 (m, 5H); MS (ESI+): 515 ([M+NH4]+).

Example 204-243 Examples 204 to 243 were prepared according to same procedure as Example 203-(3) from corresponding Fmoc-amino acid-Wang resin listed in below table. Exam 1H-NMR in MS(positive yield yield ple # compound structure CD3OD mode) (mq) (%) 0.59 (s, 6H), 0.87 (s, 9H), 3-[2-(4-{1-Ethyl-1- 2.07 (q, 4H), [4-(3-hydroxy-4,4- 2.19 (s, 3H), dimethyl-pentyl)-3- 2.22 (s, 3H), methyl-phenyl]- L j 2.43 (t, 2H), 529 1 ,U I U propyl}-2-methyl- 3.15 (d, 1H), [M+NH4]+ phenoxy)- HO_^ S /^ XJ I 3.52 (t, 2H), acetylamino]- O o i I OH 4.47 (s, 2H), propionic acid 6.72 (d, 1H), 6.88-7.05 (m, 5H)

0.63 (t, 6H), 4-[2-(4-{1-Ethyl-1- 0.91 (s, 9H), [4-(3-hydroxy-4,4- I I 2.08 (q, 4H), dimethyl-pentyl)-3- 2.26 (S1 3H), methyl-phenyl]- LJ 2.28 (s, 3H), 543 9Ω^ propyl}-2-methyl- , , x o\ /\ ^- HN. ^~x_^ IP_ ^TJ I ■ 3.19 (d, 1H), 2.1 20 [M+NH4]+ phenoxy)- HO ^^^^ T ° T^ • 4.52 (S, 2H), acetylamino]- o I I OH 6.75 (d, 1H), butyrio acid 6.90-7.07 (m, 5H)

0.59 (t, 6H), 0.87 (s, 9H), 2(S)-[2-(4-{1-Ethyl- 1.42 (d, 3H), 1-[4-(3-hydroxy- I I 2.04 (q, 4H), 4,4-dimethyl- 2.22 (s, 3H), pentyl)-3-methyl- 2.24 (s, 3H), 529 206 phenyl]-propyl}-2- 0 H fYY methyl-phenoxy)- #^^J< 1.2 12 3.18 (d, 1H), [M+NH4f 4.28 (q, 1H), acetylamino]- OH 4.48 (s, 2H), propionic acid 6.75 (d, 1H), 6.89-7.05 (m ,5H) 0.62 (t, 6H), 0.91 (s, 9H), 2(R)-[2-(4-{1-Ethyl- 1.48 (d, 3H), 1-[4-(3-hydroxy- I I 2.10 (q, 4H), 4,4-dimethyl- 2.25 (s, 3H), pentyl)-3-methyl- 2.26 (s, 3H), 529 207 1.7 17 phenyl]-propyl}^2- HO^ ft HN^O^ f∏ ^ 3.19 (d, 1H), [M+NH4]+ methyl-phenoxy)- 4.52 (q, 1H), acetylamino]- OH 4.56 (s, 2H), propionic acid 6.80 (d, 1H), 6.92-7.05 (m, 5H) 0.59 (t, 6H), 0.84 (t, 3H), 2(S)-[2-(4-{1-Ethyl- 0.87 (s, 9H), 1-[4-(3-hydroxy- I I 2.06 (q, 4H), 4,4-dimethyl- 2.24 (s, 3H), 9∏ft pentyl)-3-methyl- 2.25 (s, 3H), 543 1 n 10 phenyl]-propyl}-2- o H (T T Y 3.17 (d, 1H), [M+NH4f methyl-phenoxy)- 4.34 (t, 1H), ylamino]- K^ O ' ' T acet OH 4.52 (s, 2H), butyric acid 6.77 (d, 1H), 6.89-7.04 (m, 5H) 0.59 (t, 6H), 2(S)-[2-(4-{1-Ethyl- 0.86 (s, 9H), 1-[4-(3-hydroxy- I I 0.87 (t, 3H), 4,4-dimethyl- 2.05 (q, 4H), pentyl)-3-methyl- 3.17 (s, 1H), 557 phenyl]-propyl}-2- j IyTY T I 4.35 (d, 1H), [M+NH4]+ methyl-phenoxy)- HoΛ o ^ HN^o T 4.52 (d, 2H), acetylamino]- 1 T OH 6.75 (d, 1H), pentanoic acid I 6.88-7.04 (m, 5H)

0.59 (t, 6H), 0.87 (s, 9H), 2(R)-[2-(4-{1-Ethyl- 0.88 (t, 3H), 1-[4-(3-hydroxy- 2.07 (q, 4H), 4,4-dimethyl- L J 2.24 (S, 3H), pentyl)-3-methyl- 2.25 (s, 3H), 557 210 0.6 phenyl]-propyl}-2- HJLVVC∏C 3.15 (s, 1H), 6 [M+NH4]+ methyl-phenoxy)- ' OH 4.34 (t, 1H), acetylamino]- \ o I 4.50 (d, 2H), pentanoic acid 6.74 (d, 1H), 6.88-7.04 (m, 5H) 0.63 (t, 6H), 0.91 (s, 9H), 2(S)-[2-(4-{1-Ethyl- 0.92 (t, 3H), 1-[4-(3-hydroxy- 2.11 (q, 4H), 4,4-dimethyl- 2.28 (s, 6H), pentyl)-3-methyl- 571 211 3.20 (d, 1H), 1.2 phenyl]-propyl}-2- \ H JM U 11 4.45 (dd, 1H), [M+NH4]+ methyl-phenoxy)- I OH 4.57 (d, 2H), acetylamino]- 6.78 (d, 1H), hexanoic acid 6.92-7.07 (m, 5H) 0.59 (t, 6H), 0.87 (s, 9H), 2(R)-[2-(4-{1-Ethyl- 0.87 (t, 2H), 1-[4-(3-hydroxy- 2.06 (q, 4H), 4,4-dimethyl- L j 2.24 (s, 3H), pentyl)-3-methyl- 2.25 (s, 3H), 571 212 0.4 phenyl]-propyl}-2- ?\ H i T I 3.15 (d, 1H), 4 [M+NH4]+ methyl-phenoxy)- ' OH 4.35 (t, 1H), acetylamino]- 4.51 (d, 2H), hexanoic acid =^ ° 6.74 (d, 1H), 6.88-7.05 (m, 5H) 0.57 (t, 6H), 0.86-0.90 (m, 2(S)-[2-(4-{1-Ethyl- 6H), 0.88 (s, 1-[4-(3-hydroxy- I 9H), 2.05 (q, 4,4-dimethyl- 4H), 2.22 (s, pentyl)-3-methyl- <J I lf l 3H), 2.23 (S, 557 1 3 phenyl]-propyl}-2- o H l ' 3H), 3.14 (d, [M+NH4]+ methyl-phenoxy)- acetylamino]-3- T^ n r ■ 1H), 4.34 (d, .54 (s, methyl-butyric acid sK ° 1 OH 1H), 4 2H), 6.75 (d, 1H), 6.90-7.02 (m, 5H) 0.59 (t, 6H), 0.81-0.91 (m, 2(R)-[2-(4-{1-Ethyl- 6H), 2.06 (q, 1-[4-(3-hydroxy- 4H), 2.24 (s, 4,4-dimethyl- 3H)1 2.26 (S, pentyl)-3-methyl- 557 214 • 3H), 3.16 (d, phenyl]-propyl}-2- 0.4 . 1H), 4.31 (d, [M+NH4]+ methyl-phenoxy)- H0JO 1H), 4.55 (d, acetylamino]-3- rY^ 1H), 6.76 (d, methyl-butyric acid 1H), 6.89-7.03 (m, 5H)

(2S,3S)-2-[2-(4-{1- 0.63 (t, 6H), Ethyl-1-[4-(3- 0.90-0.97 (m, hydroxy-4,4- 6H), 2.08 (q, dimethyl-pentyl)-3- 4H), 2.28 (s, methyl-phenyi]- 3H), 3.20 (S, 571 215 ∏ H 0.7 propyl}-2-methyl- 1H), 4.49 (d, [M+NH4]+ phenoxy)- 1H), 4.61 (S, acetylamino]-3- 2H), 6.79 (d, methyl-pentanoic 1H), 6.93-7.07 acid (m ,5H)

0.59 (t, 6H), (2R,3R)-2-[2-(4-{1- 0.86-0.90 (m, Ethyl-1-[4-(3- 15H), 2.06 (q, hydroxy-4,4- 4H), 2.24 (s, dimethyl-pentyl)-3- 3H), 2.25 (s, methyl-phenyl]- 571 216 3H), 3.16 (d, 0.4 propyl}-2-methyl- phenoxy)- Y^σ 1H), 4.34 (d, [M+NH/ 1H), 4.57 (d, acetylamino]-3- 2H), 6.75 (d, methyl-pentanoic 1H), 6.89-7.03 acid r- (m, 5H)

0.59 (t, 6H), 2(S)-[2-(4-{1-Ethyl- 0.87 (s, 9H), 1-[4-(3-hydroxy- 0.86-0.90 (m, 4,4-dimethyl- 6H), 2.06 (q, pentyl)-3-methyl- 4H), 2.24 (s, 571 217 phenyl]-propyl}-2- 6H), 3.15 (d, 0.6 methyl-phenoxy)- [M+NH4]+ 1H), 4.40 (t, acetylamino]-4- OH 1H), 6.73 (d, methyl-pentanoic 1H), 6.90-7.03 acid (m, 5H)

0.59 (t, 6H), 2(R)-[2-(4-(1 -Ethyl- 0.87 (s, 9H), 1-[4-(3-hydroxy- 0.86-0.92 (m, 4,4-dimethyI- 6H), 2.06 (s, pentyl)-3-methyl- 218 phenyl]-propyl}-2- Il H 6H), 3.18 (d, 571 2.0 18 methyl-phenoxy)- H0ATNγ^σ 1H), 4.41 (t, [M+NH4]+ 1H), 4.43-4.58 acetylamino]-4- (m, 2H), 6.73 methyl-pentanoic (d, 1H), 6.89- acid X0 7.03 (m, 5H) H

444

0.59 (t, 6H), (S)-Cyclohexyl-[2- 0.87 (s, 9H),2.06 (q, (4-(1-ethyl-1-[4-(3- 4H), 2.24 (s, hydroxy-4,4- 3H), 2.25 (s, dimethyl-pentyl)-3- ■ 3H), 3.15 (d, 597 219 methyl-phenyl]- - 1H), 4.31 (d, 1.5 13 propyl}-2-methyl- [M+NH4]+ OH 1H), 4.52-4.59 phenoxy)- (m, 2H), acetylamino]-acetic 6.74(d, 1H), acid 6.89-7.01 (m, 5H)

(S)-3-Cyclohexyl-2- 0.59 (t, 6H), [2-(4-{1-ethyl-1-[4- 0.87 (s, 9H), (3-hydroxy-4,4- 2.06 (q, 4H), dimethyl-pentyl)-3- 2.24 (S1 6H), 611 220 methyl-phenyl]- 3.16 (d, 1H), 0.6 propyl}-2-methyl- 4.48-4.60 (m, [IVH-NH4]' phenoxy)- OH 3H), 6.72 (d, acetylamino]- 1H), 6.92-7.03 propionic acid (m, 5H)

0.58 (t, 6H), (S)-1-[2-(4-{1-Ethyl- 0.87 (s, 9H), 1-[4-(3-hydroxy- 2.06 (q, 4H), 4,4-dimethyl- 2.24 (s, 3H), pentyl)-3-methyl- 555 221 3.16 (d, 1H), 0.4 phenyl]-propyl}-2- 4.48-4.60 (m, [M+NH4f methyl-phenoxy)- acetyl]-pyrrolidine- OH 3H), 6.72 (d, 1H), 6.92-7.03 2-carboxylio acid (m, 5H)

0.60 (t, 6H), 0.87 (s, 9H), (S)-[2-(4-{1-Ethyl-1- 2.05 (q, 4H), [4-(3-hydroxy-4,4- 2.24 (s, 3H), dimethyl-pentyl)-3- 2.28 (S1 3H), O methyl-phenyl]- . 3.18 (d, 1H), 591 222 propyl}-2-methyl- .4.53-4.60 (m, 0.6 [M+NH4]+ phenoxy)- 2H)1 5.35 (s, acetylamino]- 1H), 6.72 (d, phenyl-acetic acid 1H), 6.90-7.04 (m, 5H)1 7.26- 7.38 (m, 5H)

2(S)-[2-(4-{1-Ethyl- 0.59 (t, 6H), 1-[4-(3-hydroxy- 0.87 (S1 9H), 4,4-dimethyl- 2.06-2.10 (m pentyl)-3-methyl- ,7H)1 2.22 (s, 605 223 phenyl]-propyl}-2- ^3H), 4.39-4.53 0.9 methyl-phenoxy)- (m, 2H), 4.70 Λ+NH4f acetylamino]-3- OH (t, 1H), 6.59 (d, phenyl-propionic 1H), 6.90-7.17 acid (m, 10H) 2(R)-[2-(4-{1-Ethyl- 0.59 (t, 6H), 1-[4-(3-hydroxy- 0.86 (s ,9H), 4,4-dimethyl- 2.05-2.10 (m, pentyl)-3-methyl- , 7H), 2.22 (s, 605 224 phenyl]-propyi}-2- .3H), 4.36-4.51 3.6 31 mβthyl-pheπoxy)- (m, 2H), 4.65 [M+NH4]+ acetylamino]-3- OH (t, 1H), 6.60 (d, phenyl-propionic 1H), 6.90-7.16 acid (m, 10H)

2(S)-[2-(4-{1-Ethyl- 0.60 (t, 6H), 1-[4-(3-hydroxy- 1.29 (s, 9H), 4,4-dimethyl- 2.05-2.11 (m, pentyl)-3-methyl- 7H), 2.22 (s, 621 225 phenyl]-propyl}-2- 3H), 3.17 (d, 2.2 18 methyl-phenoxy)- [M+NH4]+ OH 1H), 4.40-4.53 acetylamino]-3-(4- (m, 2H), 4.63 hydroxy-phenyl)- (t, 1H)1 6.60- propionic acid 7.03 (m, 10H)

2(R)-[2-(4-{1-Ethyl- 0.60 (t, 6H), 1-[4-(3-hydroxy- 0.87 (s, 9H), 4,4-dimethyl- 2.06-2.11 (m, pentyl)-3-methyl- ' 7H), 2.21 (s, 621 226 phenyl]-propyl}-2- ' 3H), 3.15 (d, 2.9 24 methyl-phenoxy)- OH 1H), 4.37-4.52 [M+NH4]+ acetylamino]-3-(4- (m ,2H), 4.62 hydroxy-phenyl)- (t, 1H), 6.59- propionic acid 7.03 (m ,10H)

0.63 (t, 6H), (2S,3R)-2-[2-(4-(1- 0.91 (s, 9H), Ethyl-1-[4-(3- 1.13 (d, 3H)1 hydroxy-4,4- 2.12 (q, 4H), dimethyl-pentyl)-3- 2.27 (S1 3H), methyl-phenyl]- 559 227 . 2.29 (S1 3H), propyl}-2-methyl- 1.3 12 . 3.19 (d, 1H), [M+NH4]+ pheπoxy)- 4.27-4.34 (m acetylamino]-3- OH ,2H), 4.59 (s, hydroxy-butyric 2H), 6.78-7.07 acid (m, 6H)

(2R,3S)-2-[2-(4-{1- 0.59 (t ,6H), Ethyl-1-[4-(3- 0.87 (S, 9H), hydroxy-4,4- 1.10 (d, 3H), dimethyl-pentyl)-3- 2.04 (q, 4H), methyl-phenyl]- 2.24 (s, 3H), 559 228 propyl}-2-rτiethyl- 0.7 2.25 (d, 3H), [M+NH4]+ phenoxy)- 3.15 (d, 1H)1 acetylamino]-3- OH 4.28-4.59 (m, hydroxy-butyric 4H), 6.78-7.03 acid (m, 6H) 0.63 (t, 6H), 2(S)-[2-(4-{1-Ethyl- 0.91 (S, 9H), 1-[4-(3-hydroxy- 2.11 (a, 4H), 4,4-dimethyl- 2.28 (s, 3H), pentyl)-3-methyl- 2.31 (s, 3H), 545 229 phenyl]-propyl}-2- 3.19 (d, 1H), 1.7 16 methyl-phenoxy)- 3.94 (d, 2H), [M+NH4]+ acetylamino]-3- OH 4.37 (t, 1H), hydroxy-propionic 4.55 (S, 2H), acid 6.82-7.07 (m, 6H)

0.59 (t, 6H), 2(R)-[2-(4-{1-Ethyl- 0.87 (S, 9H), 1-[4-(3-hydroxy- 2.07 (q, 4H), 4,4-dimethyl- 3.18 (d, 1H), pentyl)-3-methyl- 3.90-3.93 (m, 545 230 phenyl]-propyl}-2- 2.0 19 ' 2H), 4.37 (t, methyl-phenoxy)- [M+NH4]+ IH), 4.50-4.55 acetylamino]-3- OH (m, 2H), 6.79 hydroxy-propionic (d, 1H), 6.90- acid 7.03 (m, 5H)

0.62 (t, 6H), (2S,4R)-1-[2-(4-{1- 0.91 (S, 9H), Ethyl-1-[4-(3- 2.08 (q, 4H), hydroxy-4,4- 2.22 (s, 3H), dimethyl-pentyl)-3- 2.27 (s, 3H), 571 231 methyl-phenyl]- 3.19 (d, 1H), 1.6 14 propyl}-2-methyl- [M+NH4]+ 3.69-3.72 (m, phenoxy)-acetyl]-4- OH 1H), 4.43-4.75 hydroxy-pyrrolidine- (m, 3H), 6.77- 2-carboxylic acid 7.07 (m, 6H)

0.63 (t, 6H), 0.91 (s, 9H), (S)-5-Amino-2-[2- 2.10 (q, 4H), (4-{1-ethyl-1-[4-(3- 2.28 (s, 3H), hydroxy-4,4- 2.30 (s, 3H), dimethyl-pentyl)-3- 2.99 (t, 2H), 572 232 methyl-phenyl]- 2.7 24 3.15 (d, 1H), propyl}-2-methyl- [M+NH4]+ OH 4.32 (t, 1H), phenoxy)- 4.54 (s, 2H), acetylamino]- 6.80 (d, 1H), pentanoic acid 6.94-7.07 (m, 5H) 0.63 (t, 6H), 0.91 (s, 9H), (R)-5-Amino-2-[2- 2.11 (q, 4H), (4-(1-ethyl-1-[4-(3- 2.28 (s, 3H), hydroxy-4,4- dimethyl-pentyl)-3- O H 2.29 (s, 3H), 2.99 (t, 2H), 572 233 methyl-phenyl]- HOJ^N^O. 3.5 32 3.19 (d, 1H), propyl}-2-methyl- [M+NH4]+ 4.33 (t, 1H), phenoxy)- 4.54 (s, 2H), acetylamino]- 6.79 (d,1H), pentanoic acid V NH7 6.93-7.08 (m, 5H) 0.59 (t, 6H), 0.87 (s, 9H), (S)-6-Amino-2-[2- 2.06 (q, 4H), (4-{1-ethyl-1-[4-(3- 2.24 (s, 3H), hydroxy-4,4- 2.25 (S1 3H), dimethyl-pentyl)-3- 2.88 (t, 2H), 586 234 methyl-phenyl]- 3.15 (d, 1H), 2.3 20 propyl}-2-methyl- [M+NH4]+ OH 4.31 (t, 1H), phenoxy)- 4.45 (s, 2H), acetylamino]- 6.75 (d, hexanoic acid 1H),6.92-7.03 (m, 5H) 0.59 (t, 6H), 0.87 (s, 9H), (R)-6-Amino-2-[2- 2.06 (q, 4H), (4-{1-ethyl-1-[4-(3- 2.24 (s, 3H), hydroxy-4,4- O dimethyl-pentyl)-3- H 2.26 (S, 3H), 2.88 (t, 2H), 586 235 methyl-phenyl]- HO-^N^o- 1.3 11 3.15 (d, 1H), propyl}-2-methyl- [M+NH4]+ 4.31 (t, 1H), phenoxy)- 4.50 (S, 2H), acetylamino]- 6.76 (d, 1H), hexanoic acid NH2 6.90-7.03 (m, 5H)

2(S)-[2-(4-{1-Ethyl- 0.59 (t, 6H), 1-[4-(3-hydroxy- 0.87 (S, 9H), 4,4-dimethyl- 2.06 (q, 4H), pentyl)-3-methyl- , 2.24 (S, 6H), 573 236 phenyl]-propyl}-2- ' 3.15 (d, 1H), 1.9 17 [M+NH4]+ methyl-phenoxy)- 4.47-4.59 (m, acetylamino]- OH 3H), 6.75-7.03 succinic acid (m, 6H)

0.59 (t, 6H), 2(R)-[2-(4-{1-Ethyl- 0.87 (S, 9H), 1-[4-(3-hydroxy- 2.04 (q, 4H), 4,4-dimethyl- pentyl)-3-methyl- O 2.24 (s, 6H), 573 237 3.15 (d, 1H), 0.6 phenyl]-propyl}-2- 4.46-4.60 (m, [M+NH4]+ methyl-phenoxy)- OH 3H), 6.77 (d, acetylamino]- 1H), 6.88-7.03 succinic acid (m, 5H)

0.58 (t, 6H), 0.87 (s, 9H), 2(S)-[2-(4-{1-Ethyl- 2.06 (q, 4H), 1-[4-(3-hydroxy- 2.24 (s, 3H), 4,4-dimethyl- 2.26 (S, 3H), pentyl)-3-methyl- 587 238 3.15 (d, 1H), 3.0 26 phenyl]-propyl}-2- [M+NH4]+ ' 4.37 (t, 1H), methyl-phenoxy)- OH 4.51 (S, 2H), acetylamino]- 6.76 (d, 1H), pentanedioic acid HO^ ^O 6.91-7.03 (m, 5H) 0.59 (t, 6H), 0.87 (s, 9H), 2(R)-[2-(4-{1-Ethyl- 2.06 (q, 4H), 1-[4-(3-hydroxy- 2.24 (s, 3H), 4,4-dimethyl- 2.25 (S, 3H), pentyl)-3-methyl- 587 239 3.15 (d, 1H), phenyl]-propyl}-2- 2.3 20 4.32-4.38 (m, [M+NH4]+ methyl-phenoxy)- OH 1H), 4.50 (s, acetylamino]- 2H), 6.76 (d, pentanedioic acid 1H), 6.88-7.03 (m, 5H)

0.60 (t, 6H), 2(S)-[2-(4-{1-Ethyl- 0.91 (S, 9H), 1-[4-((S)-3-hydroxy- 2.09 (q, 4H), 4,4-dimethyl- 2.28 (s, 3H), pentyl)-3-methyl- , 2.29 (s, 3H), 572 240 phenyl]-propyl}-2- ^N 3.9 35 ' 2.79 (d, 2H), methyl-phenoxy)- HO [M+NH4]+ 3.19 (d, 1H), acetylamino]- 4.53-4.63 (m, succinamic acid 3H), 6.78-7.05 NH2 (m, 6H)

0.63 (t, 6H), 2(R)-[2-(4-{1-Ethyl- 0.91 (s, 9H), 1-[4-((S)-3-hydroxy- 2.10 (q, 4H), 4,4-dimethyl- 2.28 (s, 3H), pentyl)-3-methyl- O 2.29 (s, 3H), 572 241 1.1 10 phenyl]-propyl}-2- 3.20 (d, 1H), [M+NH4]+ methyl-phenoxy)- 4.53 (d, 2H), acetylamino]- OH 4.64 (t, 1H), succinamic acid 6.79-7.04 (m, 6H)

(S)-4-Carbamoyl-2- 0.60 (t, 6H), [2-(4-{1-ethyl-1-[4- 0.91 (s, 9H), ((S)-3-hydroxy-4,4- 2.07 (q, 4H), dimethyl-pentyl)-3- 2.26 (s, 3H), methyl-phenyl]- - 2.28 (S, 3H), 586 242 2.8 25 propyl}-2-methyl- - 3.20 (d, 1H), [M+NH4]+ phenoxy)- OH 4.36-4.38 (m, acetyiamiπo]- 1H), 4.55 (s, butyric acid 2H), 6.78-7.07 H9N' (m, 6H)

(R)-4-Carbamoyl-2- 0.58 (t, 6H), [2-(4-{1-ethyl-1-[4- 0.87 (S, 9H), ((S)-3-hydroxy-4,4- 2.07 (q, 4H), dimethyl-pentyl)-3- 2.24 (s, 3H), methyl-phenyl]- - 2.26 (s, 3H), 586 243 3.2 28 propyl}-2-m8thyl- HO ~ 3.16 (d, 1H), [M+NH4]+ phenoxy)- OH 4.35-4.39 (m acetylamino]- ,1H), 4.51 (s, butyric acid 2H), 6.78-7.05 HoN (m, 6H) Starting Fmoc-amino acid-Wang resin

amino acid loading on reacted resin Example # Fmoc-amino acid-Wang resin resin (mg) (mmol/g) 204 Fmoc-beta-Ala-Wang resin 0.52 38.5 205 Fmoc-4-Abu-Wang resin 0.41 48.8 206 Fmoc-L-Ala-Wang resin 0.78 25.6 207 Fmoc-D-Ala-Wang resin 0.54 37.0 208 Fmoc-L-Abu(2)-Wang resin 0.40 50.0 209 Fomc-L-Nva-Wang resin 0.67 29.9 210 Fmoc-D-Nva-Wang resin 0.76 26.3 211 Fmoc-L-Nle-Wang resin 0.73 27.4 212 Fmoc-D-Nle-Wang resin 0.65 30.8 213 Fmoc-L-Val-Wang resin 0.80 25.0 214 Fmoc-D-Val-Wang resin 0.65 30.8 215 Fmoc-L-lle-Wang resin 0.86 23.3 216 Fmoc-D-lle-Wang resin 0.59 33.9 217 Fmoc-L-Leu-Wang resin 0.86 23.3 218 Fmoc-D-Leu-Wang resin 0.56 35.7 219 Fmoc-L-Chg-Wang resin 0.71 28.2 220 Fmoc-L-Cha-Wang resin 0.72 27.8 221 Fmoc-L-Pro-Wang resin 0.72 27.8 222 Fmoc-L-Phg-Wang resin 0.75 26.7 223 Fmoc-L-Phe-Wang resin 0.78 25.6 224 Fmoc-D-Phe-Wang resin 0.52 38.5 225 Fmoc-L-Tyr(tBu)-Wang resin 0.79 25.3 226 Fnoc-D-Tyr(tBu)-Wang resin 0.66 30.3 227 Fmoc-L-Thr(tBu)-Wang resin 0.71 28.2 228 Fmoc-D-Thr(tBu)-Wang resin 0.76 26.3 229 Fmoc-L-Ser(tBu)-Wang resin 0.81 24.7 230 Fmoc-D-Ser(tBu)-Wang resin 0.74 27.0 231 Fmoc-L-Hyp(tBu)-Wang resin 0.77 26.0 232 Fmoc-L-Orn(Boc)-Wang resin 0.48 41.7 233 Fmoc-D-Orn(Boc)-Wang resin 0.30 66.7 234 Fmoc-L-Lys(Boc)-Wang resin 0.55 36.4 235 Fmoc-D-Lys(Boc)-Wang resin 0.69 29.0 236 Fmoc-L-Asp(OtBu)-Wang resin 0.59 33.9 237 Fmoc-D-Asp(OtBu)-Wang resin 0.61 32.8 238 Fmoc-L-GIu(OtBu)-Wang resin 0.68 29.4 239 Fmoc-D-Glu(OtBu)-Wang resin 0.71 28.2 240 Fmoc-L-Asn(Trt)-Wang resin 0.54 37.0 241 Fmoc-D-Asn(Trt)-Wang resin 0.50 40.0 242 Fmoc-L-Gln(Trt)-Wang resin 0.51 39.2 243 Fmoc-D-Gln(Trt)-Wang resin 0.73 27.4

Example 244 Preparation of 3-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-pentyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol

(1 ) Preparation of 4-{1 -[4-(2,2-Dimethyl-[1 )3]dioxolan-4-ylmethoxy)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenol

To a solution of 3,3-bis-(4-hydroxy-3-methyl-phenyl)-pentane (2.91 g, 10.2 mmol) in DMSO (26 ml) were added t-BuOK (1.1 g, 9.80 mmol) and 2,2- dimethyl-1 ,3-dioxolan-4-yl-methyl p-toluensulfonate (2.3 g, 8.03 mmol) and the mixture was stirred at 60 degrees C for 8 h. The reaction mixture was poured into sat. NH4CI aq. and the products were extracted with AcOEt. The extracts were washed with water and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with CH2CI2:AcOEt (50/1 to 2/1) to give the title compound (1.37 g, 43%) as colorless oil. 1H NMR (CDCI3, 400 MHz): 0.61 (6H, t, J= 7.2 Hz), 1.40 (3H, s), 1.46 (3H, s), 2.00 (4H, q, J=7.5 Hz), 2.15 (3H, s), 2.19 (3H, s), 3.89-4.18 (4H, m), 4.60 (1 H, s), 6.67 (2H, m), 6.83-6.96 (4H, m).

(2) Preparation of Trifluoro-methanesulfonic acid 4-{1-[4-(2,2-dimethyl- [1 ,3]dioxolan-4-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2- methyl-phenyl ester

OTf

To a solution of 4-{1-[4-(2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenol (compound prepared in Example 244- (1)) (1.57 g, 3.939 mmol) in CH2CI2 (40 ml) under N2 atmosphere were added Tf2O (0.969 ml, 5.909 mmol) and pyridine (0.954 ml, 11.82 mmol) and the mixture was stirred for 30 min. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extracted with CH2CI2. The extracts were dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :20) to give the title compound (1.5 g, 50%) as colorless oil. 1H-NMR (CDCI3): 0.59 (6H, t, J = 7.25 Hz), 1.40 (3H1 s), 1.46 (3H, s), 1.97-2.11 (4H, m), 2.16 (3H, s), 2.31 (3H, s), 3.90-4.20 (4H, m), 4.40-4.52 (1 H, m), 6.70 (1 H, d, J = 8.57 Hz), 6.81-6.95 (2H, m), 7.00-7.15 (3H, m).

(3) Preparation of 3-(4-{1-[4-(2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-propionic acid ethyl ester

OTf

To a solution of Trifluoro-methanesulfonic acid 4-{1 -[4-(2,2-dimethyl- [1 ,3]dioxolan-4-ylmethoxy)-3-methyl-phenyl]-1-ethyl-propyl}-2- methyl-phenyl ester (compound prepared in Example 244-(2)) (310 mg, 0.584 mmol) in DMF (1.0 ml) was added Pd(PPh3)4 (67 mg) and the mixture was stirred for 5 min. To the reaction mixture, 3-Ethoxy-3-oxopropylzinc bromide 0.5 M THF solution (2.9 ml, 1.45 mmol) and HMPA (1.45 ml, 8.30 mmol) were added and the mixture was stirred at 60 degrees C for 3.5 h. The reaction mixture was poured into water and the products were extracted with AcOEt. The extracts were dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :5) to give the title compound (175 mg, 62%) as colorless oil. 1H NMR (CDCI3); 0.58 (6H, t, J= 7.4 Hz), 1.24 (3H, t, J= 7.1 Hz), 1.40 (3H, s), 1.46 (3H, s), 2.01 (4H, q, J=7.4 Hz), 2.15 (3H, s), 2.25 (3H, s), 2.56 (2H, t, J=7.4 Hz), 2.89 (2H, t, J=8.5 Hz), 3.93-4.11 (m, 6H), 4.46 (m, 1H), 6.68 (1H, d, J= 8.5 Hz), 6.94 (5H, m). (4) Preparation of 1-(4-{1-[4-(2,2~Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-pentan-3-ol

.OEt

To a solution of 3-(4-{1-[4-(2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-propionic acid ethyl ester (compound prepared in Example 244-(3)) (37.5 mg, 0.078 mmol) in THF (2 ml) at -78 degrees C under N2 atmosphere was added EtLi (ca.0.4 mol/l, 0.585 ml, 0.234 mmol) and the mixture was stirred for 1 h. The reaction mixture was poured into sat. NH4CI aq. and the products were extracted with AcOEt. The extracts were washed with water and brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by preparative TLC (Hex:AcOEt 2:1) to give the title compound (30.4 mg, 79%) as colorless oil. 1H-NMR (CDCI3): 0.59 (6H, t, J = 7.08 Hz)1 0.91 (6H, t, J = 7.42 Hz)1 1.40 (3H, s), 1.46 (3H, s), 1.48-1.70 (6H, m), 1.95-2.05 (4H, m), 2.16 (3H, s), 2.25 (3H1 s), 2.50-2.61 (2H, m), 3.89-4.20 (4H, m), 4.40-4.50 (1 H, m), 6.68 (1 H, d, J = 8.24 Hz), 6.85-7.03 (5H, m).

(5) Preparation of 3-(4-{1 -Ethyl- 1-[4-(3-ethyl-3-hydroxy-pentyl)-3-methyl-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol

To a solution of 1-(4-{1-[4-(2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-pentan-3-ol (compound prepared in Example 244-(4)) (30.4 mg, 0.061 mmol) in THF-H2O(10:1 , 3.3 ml) was added CSA (42.7 mg, 0.184 mmol) and the mixture was stirred at 50 δδdegrees C for 5 h. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extracted with CH2CI2. The extracts were dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by preparative TLC (AcOEt) to give the title compound (19.4 mg, 70%) as colorless oil. 1H-NMR (CDCI3): 0.59 (6H, t, J = 7.09 Hz), 0.91 (6H, t, J = 7.42 Hz)1 1.48-1.70 (6H, m), 1.95-2.10 (4H, m), 2.17 (3H, s), 2.25 (3H, s), 2.50-2.62 (2H, m), 3.72- 3.90 (2H, m), 3.98-4.15 (3H, m), 6.69 (1 H, d, J = 8.25 Hz), 6.85-7.03 (5H, m); MS (ESI+) : 474 ([M+NH4]+).

Example 246 Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-1 -methyl-pent- 1 - enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-p entanoic acid

HOOC OH

(1) Preparation of (E)-3-{4-[1-Ethyl-1-(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenyl}-but-2-enoic acid ethyl ester

OTf CO2Et

To a solution of Trifluoro-methanesulfonic acid4-[1-ethyl-1-(4-hydroxy-3-methyl- phenyl)-propyl]-2- methyl-phenyl ester (compound prepared in Example 1-(1)) (52.5 mg, 0.105 mmol) in DMF(0.35 ml) were added Crotonic acid ethyl ester (0.052 ml, 0.419 mmol), NaHCO3 (37 mg, 0.440 mmol), dppp(4.3 mg, 0.0104 mmol), LiBr(6.3 mg, 0.0725 mmol) and PdCI2 (PPh3)2 (7.4 mg, 0.0105 mmol) and the mixture was stirred at 140 degrees C for 12h. The reaction mixture was cooled to room temperature, poured into sat. NH4CI aq. and the products were extracted with CH2Cb. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :4) to give the title compound (13.7 mg, 28%) as colorless oil. 1H-NMR (CDCI3): 0.58 (6H, t, J = 7.09 Hz), 1.28 (3H1 1, J = 7.25 Hz), 2.05 (4H, q, J = 7.26 Hz), 2.20 (3H, s), 2.22 (3H, s), 2.43 (3H, s), 4.19 (2H1 q, J = 7.25 Hz), 4.65 (1H, s), 5.76 (1H1 s), 6.66 (1H1 d, J = 8.24 Hz), 6.95 (5H, m).

(2) Preparation of 4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-1 -methyl-pent- 1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol

CO2Et

To a solution of (E)-3-{4-[1 -Ethyl-1 -(4-hydroxy-3-methyl-phenyl)-propyl]-2- methyl-phenyl}-but-2-enoic acid ethyl ester (compound prepared in Example 246-(1 ))(64 mg, 0.168 mmol) in THF(2 ml) was added EtMgBr(3M in Et2O, 0.28 ml, 0.840 mmol) at 0 degrees C under nitrogen atmosphere and the reaction mixture was stirred for 2.5 h at room temperature. The reaction mixture was poured into sat. NH4CI aq. and the products were extracted with CH2CI2. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :2) to give the title compound (30 mg, 45%) as colorless oil. 1H-NMR (CDCI3): 0.61 (6H1 1, J = 7.25 Hz), 0.97 (6H, t, J = 7.41 Hz), 1.66 (4H, q, J = 7.42 Hz), 2.03 (4H, q, J = 7.42 Hz), 2.11 (3H, d, J = 0.99 Hz), 2.21 (3H, s), 2.23 (3H, s), 4.65 (1 H, brs), 5.18 (1H, d, J = 1.16 Hz), 6.65 (1 H1 d, J = 8.41 Hz), 6.85-6.92 (5H, m).

(3) Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-1-methyl-pent-1- enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2-one

To a solution of 4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-1-methyl-pent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 246- (2)) (15 mg, 0.038 mmol) in DMF(I ml) were added K2CO3(10.5 mg, 0.076 mmol) and (S)-Dihydro-5-(toluenesulfonylmethyl)-2-(3H)furanone (20.5 mg, 0.076 mmol) and the mixture was stirred at 100 degrees C for 7 h. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extracted with AcOEt. The extracts were washed with water and brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :2) to give the title compound (15.2 mg, 81%) as colorless oil. 1H-NMR (CDCI3): 0.60 (6H, t, J = 7.25 Hz), 0.97 (6H, t, J = 7.26 Hz), 1.66 (4H, q, J = 7.26 Hz), 1.98-2.08 (4H, m), 2.11 (3H, d, J = 0.82 Hz), 2.16 (3H, s), 2.23 (3H, s), 2.25-2.85 (4H1 m), 4.05-4.20 (2H, m), 4.82-4.92 (1 H, m), 5.18 (1H, s), 6.67 (1H, d, J = 8.24 Hz), 6.85-7.00 (5H, m).

(4) Preparation of (S)-5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-1-methyl-pent- 1- enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-p entanoic acid

HOOC

To a solution of (S)-5-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-1-methyl-pent- 1- enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2-one (compound prepared in Example 246-(3)) (15.8 mg, 0.038 mmol) in MeOH (0.360 ml) was added 1 N KOH(0.180 ml) and the mixture was stirred at room temperature for 1 h. The reaction mixture was concentrated under reduced pressure and the obtained residue was purified by preparative TLC (CHCI3:MeOH=8:3, saturated with H2O) to give the title compound (15.2 mg, 81%) as colorless oil. 1H-NMR (CDCI3): 0.61 (6H, t, J = 7.09 Hz), 0.97 (6H, t, J = 7.42 Hz), 1.66 (4H1 q, J = 7.25 Hz), 1.98-2.08 (6H, m), 2.11 (3H, s), 2.19 (3H, s), 2.23 (3H, s), 2.62 (2H, t, J = 6.92 Hz), 3.85 (1 H, t, J = 9.07 Hz), 3.98 (1 H, d, J = 9.07 Hz), 4.10 (1 H, m), 5.18 (1 H, s), 6.68 (1H, d, J = 8.07Hz), 6.94 (5H, m); MS (ESI+) : 528 ([M+NH4]+). Example 247 Preparation of (S)-5-(4-{1 -[4-((E)-1 ,3-Diethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoi c acid

HOOC OH (1) Preparation of 2,2-Dimethyl-propionic acid 4-[1-ethyl-1-(3-methyl-4- trifluoromethanesulfonyloxy-phenyl)-propyl]-2-methyl-phenyl ester

HO OTf PivO OTf

To a solution of Trifluoro-methanesulfonic acid 4-[1-ethyl-1-(4-hydroxy-3-methyl- phenyl)-propyl]-2-methyl-phenyl ester(compound prepared in Example 1-(1 )) (1.75 g, 4.20 mmol) in CH2CI2 (22 ml) were added Et3N (0.643 ml, 4.64 mmol) and Pivaloyl chloride(0.566 ml, 4.60 mmol) and the mixture was stirred at 0 degrees C for 1 h and at room temperature for 1 h. The reaction mixture was poured into water and the products were extracted with CH2CI2. The extracts were dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :4) to give the title compound (1.66 g, 79%). 1H-NMR (CDCI3): 0.60 (6H, t, J = 7.14 Hz), 1.37 (9H, s), 2.05 (4H, q, J = 7.41 Hz ), 2.12 (3H, s), 2.31 (3H, s), 6.87 -7.13 (6H, m).

(2) Preparation of (E)-3-(4-{1-[4-(2,2-Dimethyl-propionyloxy)-3-methyl-phenyl]- 1- ethyl-propyl}-2-methyl-phenyl)-pent-2-enoic acid methyl ester

PivO OTf PivO -CO2Me

2,2-Dimethyl-propionic acid 4-[1 -ethyl-1 -(3-methyl-4-trifluoromethanesulfonyloxy- phenyl)-propyl]-2-methyl-phenyl ester(compound prepared in Example 247-(1 )) (945 mg, 1.89 mmol) in DMF(6.3 ml) were added Methyl trans-2-pentanoate (0.929 ml, 7.33 mmol), NaHCO3 (662 mg, 7.88 mmol), dppp(78 mg, 0.188 mmol), LiBr(117 mg, 1.35 mmol) and PdCI2 (PPh3) 2 (139 mg, 0.198 mmol) and the mixture was stirred at 150 degrees C for 12h. The reaction mixture was cooled to room temperature, poured into sat. NH4CI aq. and the products were extracted with CH2CI2. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :4) to give the title compound (253 mg, 29%) as colorless oil. 1H-NMR (CDCI3): 0.61 (6H, t, J = 7.25 Hz), 1.301 (6H, t, J = 7.09 Hz), 1.37 (9H, s), 2.06 (4H1 q, J = 7.25 Hz ), 2.13 (3H, s), 2.23 (3H, s), 2.43 (3H, s), 4.20 (4H, q, J = 7.25 Hz), 5.76 (1 H, s), 6.87 (1 H, d, J = 8.41 Hz), 6.94-7.00 (5H, m).

(3) Preparation of 2,2-Dimethyl-propionic acid 4-{1-[4-((E)-1 ,3-diethyl-3-hydroxy- pent-1 -enyl)-3-methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl ester

pivo ^r "CO2Me PivO

To a solution of (E)-3-(4-{1-[4-(2,2-Dimethyl-propionyloxy)-3-methyl-phenyl]- 1- ethyl-propyl}-2-methyl-phenyl)-pent-2-enoic acid methyl ester (compound prepared in Example 247-(2))(128.1 mg, 0.276 mmol) in THF(3 ml) was added EtMgBr (3M in Et2O, 0.552 ml, 1.656 mmol) at 0 degrees C and the mixture was stirred at room temperature for 1 h. The reaction mixture was poured into sat. NH4CI aq. and the products were extracted with CH2CI2. The extracts were dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound (124 mg, 91%) as colorless oil. 1H-NMR (CDCI3): 0.61 (6H, t, J = 7.26 Hz), 0.85 (3H, t, J = 7.42 Hz), 0.97 (6H, t, J = 7.42 Hz), 1.36 (9H, s), 1.65 (4H, q, J = 7.42 Hz), 2.06 (4H, q, J = 7.25 Hz), 2.12 (3H, s), 2.22 (3H, s), 2.64 (2H, q, J = 7.42 Hz), 5.11 (1 H, s), 6.84-7.03 (6H, m). (4) Preparation of 4-{1-[4-((E)-1 ,3-Diethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenol

PivO

To a solution of 2,2-Dimethyl-propionic acid 4-{1 -[4-((E)-1 ,3-diethyl-3-hydroxy- pent-1 -enyl)-3-methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenyl ester (compound prepared in Example 247-(3))(124 mg, 0.252 mmol) in MeOH (3 ml) was added 1 N-KOH(0.503 ml, 0.503 mmol) and the mixture was stirred at room temperature for 1.5 h and at 60 degrees C for 0.5 h. The reaction mixture was poured into sat. NH4CI aq. and the products were extracted with CH2CI2. The extracts were dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by preparative TLC (Hex:AcOEt 2:1) to give the title compound (99.5 mg, 97%) as colorless oil. 1H-NMR (CDCI3): 0.60 (6H, t, J = 7.25 Hz), 0.85 (3H, t, J = 7.42 Hz), 0.97 (6H, t, J = 7.26 Hz), 1.66 (4H, q, J = 7.25 Hz), 2.03 (4H, q, J = 7.26 Hz), 2.20 (3H, s), 2.22 (3H, s), 2.64 (2H, q, J = 7.42 Hz), 4.85 (1H, brs), 5.11 (1H, s), 6.65 (1H, d, J = 8.24 Hz), 6.85-6.98 (5H, m).

(5) Preparation of (S)-5-(4-{1-[4-((E)-1 ,3-Diethyl-3-hydroxy-pent-1-enyl)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenoxymethyl)-dihyd ro-furan-2-one

To a solution of 4-{1-[4-((E)-1 ,3-Diethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]- 1 -ethyl-propyl}-2-methyl-phenol (compound prepared in Example 247-(4)) (49 mg, 0.120 mmol) in DMF(I ml) were added K2CO3(33.2 mg, 0.240 mmol) and (S)-Dihydro-5-(toluenesulfonylmethyl)-2-(3H)furanone (64.9 mg, 0.240 mmol) and the mixture was stirred at 100 degrees C overnight. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extracted with AcOEt. The extracts were washed with water and brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by preparative TLC (Hex:AcOEt 2:1) to give the title compound (39.9 mg, 66%) as colorless oil. 1H-NMR (CDCI3): 0.60 (6H, t, J = 7.26 Hz), 0.85 (3H, t, J = 7.41 Hz), 0.97 (6H1 1, J = 7.25 Hz), 1.65 (4H, q, J = 7.26 Hz), 1.97-2.10 (4H, m), 2.16 (3H, s), 2.22 (3H, s), 2.25-2.85 (6H, m), 4.03-4.20 (2H, m), 4.83-4.92 (1 H, m), 5.11 (1 H, s), 6.67 (1 H, d, J = 8.08 Hz), 6.85-7.00 (5H, m).

(6) Preparation of (S)-5-(4-{1 -[4-((E)-1 ,3-Diethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-1 -ethyl-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

HOOC

To a solution of (S)-5-(4-{1 -[4-((E)-1 ,3-Diethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenoxymethyl)-dihydro-fura n-2-one (compound prepared in Example 247-(5)) (39.9 mg, 0.0787 mmol) in MeOH (0.854 ml) was added 1N KOH solution (0.427 ml) and the reaction mixture was stirred at room temperature for 1 h. The mixture was concentrated under reduced pressure and obtained residure was purified by preparative TLC (CHCI3:MeOH=8:3, saturated with H2O) to give the title compound (41.8 mg, quant) as colorless oil. 1H-NMR (CDCI3): 0.60 (6H, t, J = 7.09 Hz), 0.85 (3H1 1, J = 7.42 Hz), 0.97 (6H, t, J = 7.26 Hz), 1.65 (4H, q, J = 7.08 Hz), 1.90-2.05 (6H, m), 2.18 (3H, s), 2.22 (3H, s), 2.62 (4H, m), 3.85 (1H, t, J = 9.23 Hz), 3.97 (1H, d, J = 9.23 Hz), 4.10 (1H, m), 5.11 (1 H1 s), 6.68 (1H, d, J = 8.24Hz), 6.94 (5H, m); MS (ESI+) : 542 ([M+NH4]+).

Example 248 Preparation of (S)-3-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-1 -methyl-pent-1 - enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol HO^j^O OH

(1) Preparation of (E)-5-(4-{1-[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-hex- 4-en-3-ol

To a solution of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-1-methyl-pent-1-enyl) -3- methyl-phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 246- (2)) (15 mg, 0.038 mmol) in DMF(I ml) were added K2CO3(10.5 mg, 0.076 mmol) and (S)-2,2-Dimethyl-1 ,3-dioxolane-4-ylmethyl p-toluenesulfonate(21.8 mg, 0.076 mmol) and the mixture was stirred at 100 degrees C for 7 h. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extracted with AcOEt. The extracts were washed with water and brine, dried over MgSO-t, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :2) to give the title compound (13.1 mg, 68%) as colorless oil. 1H-NMR (CDCI3): 0.60 (6H, t, J = 7.26 Hz), 0.97 (6H, t, J = 7.26 Hz), 1.40 (3H, s), 1.46 (3H, s), 1.66 (4H, q, J = 7.25 Hz), 1.97-2.08 (4H, m), 2.11 (3H, s), 2.17 (3H, s), 2.23 (3H, s), 3.88-4.20 (4H1 m), 4.40-4.50 (1 H, m), 5.18 (1 H, s), 6.69 (1 H, d, J = 8.25 Hz), 6.85-7.00 (5H, m).

(2) Preparation of (S)-3-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-1-methyl-pent- 1- enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol

OH To a solution of (E)-5-(4-{1-[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-hex- 4-en-3-ol (compound prepared in Example 248-(1))(7.0 mg, 0.0138 mmol) in THF/H2O=10/1 (0.2 ml) was added CSA(6.8 mg, 0.0292 mmol) and the mixture was stirred at room temperature for 12 h. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extracted with CH2CI2. The extracts were dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :2) to give the title compound (2.0 mg, 31%) as colorless oil. 1H-NMR (CDCI3): 0.61 (6H, t, J = 7.09 Hz), 0.97 (6H, t, J = 7.41 Hz), 1.62 (4H, q, J = 7.59 Hz)1 2.03 (4H, q, J = 7.42 Hz), 2.11 (3H, s), 2.18 (3H, s), 2.23 (3H, s), 2.54 (1H, d, J = 4.78 Hz), 3.74-3.86 (2H, m), 4.03-4.12 (3H, m), 5.18 (1H, s), 6.70 (1 H, d, J = 8.41 Hz), 6.90-6.94 (5H, m).

Example 249 Preparation of (S)-3-(4-{1 -[4-((E)-1 ,3-Diethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-1-ethyl-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol

OH (1 ) Preparation of (E)-5-(4-{1-[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-hept -4-en-3-ol

To a solution of 4-{1-[4-((E)-1 ,3-Diethyl-3-hydroxy-pent-1-enyl)-3-methyl-phenyl]- 1-ethyl-propyl}-2-methyl-phenol (compound prepared in Example 247-(4)) (50 mg, 0.122 mmol) in DMF (1 ml) were added K2CO3 (33.9 mg, 0.245 mmol) and (S)-2,2-Dimethyl-1 ,3-dioxolane-4-ylmethyl p-toluenesulfonate (70.2 mg, 0.245 mmol) and the mixture was stirred at 100 degrees C overnight. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extracted with AcOEt. The extracts were washed with water and brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by preparative TLC (Hex:AcOEt 2:1) to give the title compound (35.8 mg, 56%) as colorless oil. 1H-NMR (CDCI3): 0.60 (6H, t, J = 7.25 Hz), 0.85 (3H, t, J = 7.41 Hz), 0.97 (6H, t, J = 7.25 Hz), 1.40 (3H, s), 1.46 (3H, s), 1.65 (4H, q, J = 7.26 Hz) 1.97-2.02 (4H, m), 2.17 (3H1 s), 2.22 (3H, s), 2.64 (2H, q, J = 7.42 Hz), 3.90-4.20 (4H, m), 4.40- 4.50 (1H, m), 5.11 (1H, s), 6.69 (1H, d, J = 8.41 Hz), 6.88-6.96 (5H1 m).

(2) Preparation of (S)-3-(4-{1 -[4-((E)-1 ,3-Diethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenoxy)-propane-1,2 -diol

To a solution of (E)-5-(4-{1-[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-hept -4-en-3-ol (compound prepared in Example 249-(1)) (32.7 mg, 0.063 mmol) in THF/H2O=10/1 (0.94 ml) was added CSA(31 mg, 0.133 mmol) and the mixture was stirred at room temperature for 12 h. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extracted with CH2CI2. The extracts were dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :2) to give the title compound (16.0 mg, 53%) as colorless oil. 1H-NMR (CDCI3): 0.60 (6H, t, J = 7.14 Hz), 0.85 (3H, t, J = 7.41 Hz), 0.97 (6H, t, J = 7.41 Hz), 1.64 (4H, q, J = 7.41 Hz) 2.04 (4H, q, J = 7.41 Hz), 2.18 (3H, s), 2.22 (3H, s), 2.57 (1H, d, J = 4.94 Hz), 2.64 (4H, q, J = 7.41 Hz), 3.74-3.87 (2H, m), 4.03-4.14 (3H, m), 5.11 (1 H, s), 6.71 (1 H, d, J = 8.23 Hz), 6.88-6.99 (5H, m).

Example 250 Preparation of (S)-3-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-1 -methyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol OH (1) Preparation of (E)-3-(4-{1-[4-(2,2-Dimethyl-propionyloxy)-3-methyl-phenyl]- 1- ethyl-propyl}-2-methyl-phenyl)-but-2-enoic acid ethyl ester

PivO OTf PivO ^CO2Et

To a solution of 2,2-Dimethyl-propionic acid 4-[1-ethyl-1-(3-methyl-4- trifluoromethanesulfonyloxy- phenyl)-propyl]-2-methyl-phenyl ester(compound prepared in Example 247-(1 )) (562.3 mg, 1.12 mmol) in DMF(3.7 ml) were added Crotonic acid ethyl ester (0.557 ml, 4.50 mmol), NaHCO3 (396 mg, 4.71 mmol), dppp(46 mg, 0.110 mmol), LiBr(67 mg, 0.771 mmol) and PdCI2 (PPh3)2 (79 mg, 0.113 mmol) and the mixture was stirred at 140 degrees C for 9 h. The reaction mixture was cooled to room temperature, poured into sat. NH4CI aq. and the products were extracted with CH2CI2. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :4) to give the title compound (176.8 mg, 34%) as colorless oil. 1H-NMR (CDCI3): 0.61 (6H, t, J = 7.08 Hz), 0.97 (3H, t, J = 7.41 Hz), 1.37 (9H, s), 2.06 (4H, q, J = 7.41 Hz ), 2.13 (3H, s), 2.21 (3H, s), 2.95 (4H, q, J = 7.09 Hz ), 3.73 (3H, s), 5.69 (1H, s), 6.85-7.01 (6H, m).

(2) Preparation of 2,2-Dimethyl-propionic acid 4-{1-ethyl-1-[4-((E)-3-ethyl-3- hydroxy-1 -methyl-pent-1 -enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenyl ester

PivO ^CO2Et PivO

To a solution of (E)-3-(4-{1-[4-(2,2-Dimethyl-propionyloxy)-3-methyl-phenyl]- 1- ethyl-propyl}-2-methyl-phenyl)-but-2-enoic acid ethyl ester (compound prepared in Example 250-(1 )) (177 mg, 0.381 mmol) in THF(5 ml) was added EtMgBr (3M in Et2O, 0.381 ml, 1.143 mmol) at O degrees C and the mixture was stirred at room temperature for 2 h. The reaction mixture was poured into sat. NH4CI aq. and the products were extracted with CH2CI2. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :2) to give the title compound (123 mg, 68%) as colorless oil. 1H-NMR (CDCI3): 0.61 (6H, t, J = 7.26 Hz), 0.97 (6H, t, J = 7.41 Hz)1 1.36 (9H, s), 1.66 (4H, q, J = 7.41 Hz), 2.00-216 (10H, m), 2.23 (3H, s), 5.17 (1H, s), 6.82- 7.05 (6H, m).

(3) Preparation of 2,2-Dimethyl-propionic acid 4-{1 -ethyl- 1 -[4-(3-ethyl-3-hyd roxy- 1-methyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenyl ester

PivO PivO

To a solution of 2,2-Dimethyl-propionic acid 4-{1-ethyl-1-[4-((E)-3-ethyl-3- hydroxy-1 -methyl-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheny l ester (compound prepared in Example 250-(2))(123 mg, 0.257 mmol) in EtOH(5 ml) was added Pd(OH)2(20 mg) and the mixture was stirred at room temperature under H2 atmosphere overnight. The reaction mixture was filtered through Celite and concentrated under reduced pressure to give the title compound (115 mg, 93%) as colorless oil. 1H-NMR (CDCI3): 0.58 (6H, t, J = 7.25 Hz), 1.72-1.85 (6H, m), 1.15-1.45 (16H, m), 1.65-1.75 (1H, m), 1.89-2.13 (8H, m), 2.30 (3H, s), 3.10-3.20 (1H, m), 6.80- 7.12 (6H, m).

(4) Preparation of 4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-1 -methyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenol

PivO To a solution of 2,2-Dimethyl-propionic acid 4-{1-ethyl-1-[4-(3-ethyl-3-hydroxy-1- methyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenyl ester (compound prepared in Example 250-(3)) (115 mg, 0.238 mmol) in MeOH(3 ml) was added 1 N-KOH (0.476 ml, 0.476 mmol) and the mixture was stirred at 60 degrees C for 1 h. The reaction mixture was poured into sat. NH4CI aq. and the products were extracted with CH2CI2. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 :2) to give the title compound (75.6 mg, 80%) as colorless oil. 1H-NMR (CDCI3): 0.57 (6H, t, J = 7.25 Hz), 0.73-0.83 (6H, m), 1.19 (3H, d, J = 6.93 Hz), 1.34-1.45 (4H, m), 1.66-1.73 (1 H, m), 1.91-2.05 (5H, m), 2.17 (3H, s), 2.30 (3H, s), 3.08-3.20 (1H, m), 5.05 (1H, brs), 6.61 (1H, d, J = 8.25 Hz), 6.82- 6.96 (4H, m), 7.11 (1 H, d, J = 8.07 Hz).

(5) Preparation of 5-(4-{1-[4-((R)-2,2-Dimethyl-[1,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-hexa n-3-ol

To a solution of 4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-1-methyl-pentyl)-3-methyl - phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 250-(4)) (31.1 mg, 0.078 mmol) in DMF(0.8 ml) were added K2CO3(21.7 mg, 0.156 mmol) and (S)-2,2-Dimethyl-1 ,3-dioxolane-4-ylmethyl p-toluenesulfonate (44.7 mg, 0.156 mmol) and the mixture was stirred at 100 degrees C overnight. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extracted with AcOEt. The extracts were washed with water and brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by preparative TLC (Hex:AcOEt 2:1) to give the title compound (22.6 mg, 57%) as colorless oil. 1H-NMR (CDCI3): 0.57 (6H, t, J = 7.26 Hz), 0.73-0.82 (6H, m), 1.19 (3H, d, J = 6.93 Hz), 1.30-1.40 (4H, m), 1.40 (3H, s), 1.46 (3H, s), 1.65-1.72 (1H, m), 1.88- 2.08 (5H, m), 2.15 (3H, s), 2.31 (3H, s), 3.10-3.21 (1H, s), 3.88-4.18 (4H, m), 4.41-4.50 (1 H, m), 6.68 (1H, d, J = 8.40 Hz), 6.89-6.95 (4H, m), 7.11 (1H, d, J = 8.08 Hz).

(6) Preparation of (S)-3-(4-{1 -Ethyl-1-[4-(3-ethyl-3-hydroxy-1-methyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-propane-1 ,2-diol

OH

To a solution of 5-(4-{1-[4-((R)-2,2-Dimethyl-[1 ,3]dioxolan-4-ylmethoxy)-3- methyl-phenyl]-1-ethyl-propyl}-2-methyl-phenyl)-3-ethyl-hexa n-3-ol (compound prepared in Example 250-(5))(22.6 mg, 0.044 mmol) in THF-H2O(10:1 , 1.1 ml) was added CSA(3.1 mg, 0.013 mmol) and the mixture was stirred at 60 degrees C for 5 h. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extracted with CH2CI2. The extracts were dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with EtOAc-n-Hexane (1 : 1 ) to give the title compound (13.8 mg, 67%) as colorless oil. 1H-NMR (CDCI3): 0.58 (6H, t, J = 7.26 Hz), 0.73-0.82 (6H, m), 1.19 (3H, d, J = 6.93 Hz), 1.30-1.44 (4H, m), 1.65-1.73 (1H, m), 1.90-2.08 (5H, m), 2.16 (3H1 s), 2.31 (3H, s), 3.08-3.22 (1H, m), 3.72-3.90 (2H, m), 4.00-4.18 (3H, m), 6.69 (1H, d, J = 8.41 Hz), 6.89-6.95 (4H, m), 7.11 (1H, d, J = 8.07 Hz); MS (ESI+) : 488 ([M+NH4∏.

Example 251 Preparation of (S)-5-(4-{1 -Ethyl-1 -[4-(3-ethyl-3-hydroxy-1 -methyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

HOOC (1) Preparation of (S)-5-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-1-methyl-pentyl)-3 - methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one

To a solution of 4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-1-methyl-pentyl)-3-methyl - phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 250-(4)) (44.5 mg, 0.112 mmol) in DMF(I ml) were added K2CO3(31 mg, 0.224 mmol) and (S)- Dihydro-5-(toluenesulfonylmethyl)-2-(3H)furanone (60.5 mg, 0.224 mmol) and the mixture was stirred at 100 degrees C overnight. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extracted with AcOEt. The extracts were washed with water and brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was purified by preparative TLC (Hex:AcOEt 2:1) to give the title compound (39.9 mg, 51%) as colorless oil. 1H-NMR (CDCI3): 0.57 (6H, t, J = 7.26 Hz), 0.73-0.82 (6H, m), 1.19 (3H, d, J = 6.93 Hz), 1.32-1.45 (4H, m), 1.65-1.73 (1 H, m), 1.90-2.10 (5H, m), 2.15 (3H, s), 2.31 (3H, s), 2.30-2.82 (4H, m), 3.10-3.23 (1 H, m), 4.03-4.19 (2H, m), 4.85-4.92 (1 H, m), 6.65 (1 H, d, J = 8.41 Hz), 6.88-6.95 (4H1 m), 7.11 (1 H, d, J = 8.07 Hz).

(2) Preparation of (S)-5-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-1-methyl-pentyl)-3 - methyl-phenyl]-propyl}-2-methyl-phenoxy)-4-hydroxy-pentanoic acid

HOOC OH

To a solution of (S)-5-(4-{1-Ethyl-1-[4-(3-ethyl-3-hydroxy-1-methyl-pentyl)-3 - methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-dihydro-furan -2-one (compound prepared in Example 251 -(1)) (28.4 mg, 0.057 mmol) in MeOH (1 ml) was added 1 N-KOH(0.3 ml) and the mixture was stirred at room temperature for 1 h. The mixture was concentrated under reduced pressure and obtained residure was purified by preparative TLC (CHCI3:Me0H=8:3, saturated with H2O) to give the title compound (13.3 mg, 46%) as colorless oil. 1H-NMR (CDCI3): 0.58 (6H, t, J = 7.26 Hz), 0.73-0.82 (6H, m), 1.19 (3H, d, J = 6.76 Hz), 1.32-1.47 (4H1 m), 1.65-1.72 (1 H, m), 1.80-2.10 (7H, m), 2.17 (3H1 s), 2.31 (3H, s), 2.61 (2H, t, J = 6.59 Hz), 3.08-3.21 (1 H, m), 3.80-3.90 (1 H, m), 3.95-4.15 (2H, m), 6.66 (1 H, d, J = 8.57 Hz), 6.91-6.94 (4H, m), 7.11 (1 H, d, J = 8.08 Hz); MS (ESI-) : 511 ([M-H]").

Example 252 Preparation of 4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-benzoic acid

HOoC

(1) Preparation of Trifluoromethanesulfonic acid 4-{1-ethyl-1-[4-((E)-3-ethyl-3- hydroxy-pent-1-enyl)-3-methyl-phenyl]-propyl}-2-methyl-pheny l ester

TfO

A stirred solution of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl - phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(5)) (490 mg, 1.29 mmol) in CH2CI2 (13 ml), pyridine (0.208 ml, 2.58 mmol) and trifluoromethanesulfonic anhydride (0.212 ml, 1.29 mmol) were added and the mixture was stirred at room temperature for 1 h. To the reaction mixture, H2O was added. The organic layer was separated and concentrated in vacuo. The obtained residue was chromatographed on silica gel (ethyl acetate/hexane = 0/100 to 15/85) to give the title compound (491 mg, 74%). 1H-NMR: 0.61 (t, 6H), 0.92 (t, 6H), 1.65 (q, 4H), 2.07 (q, 4H), 2.32 (s, 3H), 2.32 (S, 3H), 6.02 (d, 1H), 6.75 (d, 1H), 6.90-6.92 (m, 2H), 7.03-7.12 (m, 3H), 7.31 (d, 1H). (2) Preparation of 4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-benzoic acid methyl ester

TfO H MeO2C H

To a solution of Trifluoromethanesulfonic acid 4-{1 -ethyl-1 -[4-((E)-3-ethyl-3- hydroxy-pent-1 -enyl)-3-methyl-phenyl]-propyl}-2-methyl-phenyl ester (compound prepared in Example 252-(1)) (461 mg, 0.90 mmol) in methanol (5 ml) and DMF (9 ml) was added triethylamine (0.376 ml, 2.70 mmol) and Pd(PPh3)4 (1.04 g, 0.90 mmol) and the mixture was stirred for 2 days at 60 degrees C under CO atmosphere. The reaction mixture was separated with ethyl acetate and H2O, the organic phase was washed with brine three times, dried over MgSO4, concentrated in vacuo. The obtained residue was chromatographed on silica gel (ethyl acetate / hexane = 0/100 to 15/85) to give the title compound (299 mg, 79%). 1H-NMR: 0.62 (t, 6H), 0.92 (t, 6H), 1.64 (dq, 4H), 2.10 (q, 4H), 2.30 (s, 3H), 2.55 (s, 3H), 3.86 (s, 3H), 6.03 (d, 1H), 6.74 (d, 1H), 6.91-7.06 (m, 4H), 7.30 (d, 1H), 7.79 (d, 1H).

(3) Preparation of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl - phenyl]-propyl}-2-methyl-benzoic acid

MeO9C HO5C

To a solution of 4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-benzoic acid methyl ester (compound prepared in Example 252-(2)) (209 mg, 0.49 mmol) in MeOH (2 ml) and THF (2 ml) was added 1 N KOH solution (3 ml) and stirred for 4 h at 60 degrees C. The reaction mixture was separated with ethyl acetate and aqueous KHSO4, the organic phase was washed with brine, dried over MgSO4, concentrated in vacuo to give the title compound (199.2 mg, 99 %). 1H-NMR: 0.63 (t, 6H)1 0.92 (t, 6H), 1.64 (d, 4H), 2.11 (q, 4H)1 2.31 (s, 3H), 2.60 (s, 3H), 6.02 (d, 1H), 6.75 (d, 1H), 6.91-7.09 (m, 4H), 7.31 (d, 1H), 7.93 (d, 1H). MS (ESI+) : 390 ([M-H2O] +)

Example 253 Preparation of 3-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-benzoylamino)-propionic acid

N HOX'^-'

Preparation of 3-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3-methyl- phenyl]-propyl}-2-methyl-benzoylamino)-propionic acid

HO5C HOoC^^

To a solution of 4-{1-Ethyl~1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl - phenyl]-propyl}-2-methyl-benzoic acid (compound prepared in Example 252-(3)) (27 mg, 0.066 mmol) in CH2CI2 (0.7 ml) and triethylamine (0.028ml, 0.198 mmol) was added beta-Ala methyl ester hydrochloride (28 mg, 0.198 mmol), WSCI hydrochloride (38 mg, 0.198 mmol) and HOBt monohydrate (10 mg, 0.066 mmol), and the mixture was stirred for 16 h at room temperature. To the reaction mixture, H2O and CH2CI2 were added. The organic layer was separated, concentrated in vacuo. The resulting residue was dissolved in THF (1 ml) and MeOH (1 ml). To the mixture, 1 N aqueous KOH (1 ml) was added and the mixture was stirred for 1 h at room temperature. The reaction mixture was concentrated in vacuo, separated with ethyl acetate and aqueous KHSO4, the organic phase was washed with brine, dried over MgSO4, concentrated in vacuo. The obtained residue was chromatographed on silica gel (CH2CbZEtOH = 10/1) to give the title compound (25.9 mg, 82%). 1H-NMR: 0.61 (t, 6H), 0.91 (t, 6H), 1.64 (dq, 4H), 2.07 (q, 4H), 2.30 (s, 3H), 2.38 (s, 3H), 2.70 (t, 2H), 3.66-3.76 (m, 2H), 6.01 (d, 1H), 6.37 (t, 1H), 6.73 (d, 1H), 6.90-7.02 (m, 4H), 7.22 (d, 1H) , 7.29 (d, 1H). MS (ESI+) : 480 ([MH-H] +)

Example 254 Preparation of 4-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-benzoylamino)-butyric acid

H

Preparation of 4-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl- phenyl]-propyl}-2-methyl-benzoylamino)-butyric acid

HO2CT-T Υ^^Qj "^ HQ8CN^JI I - POM

To a solution of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl - phenyl]-propyl}-2-methyl-benzoic acid(compound prepared in Example 252-(3)) (34 mg, 0.08 mmol) in CH2CI2 (0.8 ml) and triethylamine (0.067ml, 0.48 mmol) was added gamma-aminobuthylic acid methyl ester hydrochloride (37 mg, 0.24 mmol), WSCi hydrochloride (46 mg, 0.24 mmol) and HOBt monohydrate (12 mg, 0.08 mmol), and the mixture was stirred for 18 h at room temperature. To the reaction mixture, H2O and CH2Cb were added. The organic layer was separated, concentrated in vacuo. The resulting residue was dissolved in THF (1 ml_) and MeOH (1 ml). 1 N aqueous KOH (1 ml) was added and the mixture was stirred for 1 h at room temperature. The reaction mixture was concentrated in vacuo, separated with ethyl acetate and aqueous KHSO4, the organic phase was washed with brine, dried over MgSO4, concentrated in vacuo. The obtained residue was chromatographed on silica gel (CH2CI2/EtOH = 10/1) to give the title compound (30.8 mg, 75%). 1H-NMR: 0.61 (t, 6H), 0.92 (t, 6H), 1.64 (q, 4H), 1.89-1.99 (m, 1H), 2.07 (q, 4H), 2.30 (s, 3H), 2.40 (s, 3H), 2.47 (t, 2H), 2.50 (q, 2H), 5.98-6.04 (m, 2H), 6.74 (d, 1 H), 6.93-7.03 (m, 4H), 7.23 (d, 1H) , 7.29 (d, 1H). MS (ESI+) : 494 ([M+H] +)

Example 255 Preparation of N-(4-Amino-butyl)-4-{1 -ethyl- 1-[4-((E)-3-ethyl-3-hydroxy-pent-1 - enyl)-3-methyl-phenyl]-propyl}-2-methyl-benzamide

H7N

Preparation of N-(4-Amino-butyl)-4-{1 -ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 ■ enyl)-3-methyl-phenyl]-propyl}-2-methyl-benzamide

HO2C

To a solution of 4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl - phenyl]-propyl}-2-methyl-benzoic acid (compound prepared in Example 252-(3)) (31.5 mg, 0.077 mmol) in CH2CI2 (0.8 ml) and triethylamine (0.064ml, 0.46 mmol) was added (4-Amino-butyl)-carbamic acid 9H-fluoren-9-ylmethyl ester hydrochloride (80 mg, 0.23 mmol), WSCI hydrochloride (44 mg, 0.23 mmol) and HOBt monohydrate (12 mg, 0.077 mmol), and the mixture was stirred for 16 h at room temperature. To the reaction mixture, H2O and CH2CI2 were added. The organic layer was separated, concentrated in vacuo. The resulting residue was dissolved in DMF (0.8 ml), diethylamine (0.08 ml, 0.77 mmol) was added and the mixture was stirred for 3 h at room temperature. The reaction mixture was separated with ethyl acetate and H2O, the organic phase was washed with H2O twice, dried over MgSO4, concentrated in vacuo. The obtained residue was chromatographed on silica gel (ethyl acetate/EtOH = 10/1) to give the title compound (18.3 mg, 50%). 1H-NMR: 0.61 (t, 6H), 0.92 (t, 6H), 1.49-1.58 (m, 4H), 1.64 (dq, 4H), 2.07 (q, 4H), 2.30 (S1 3H), 2.40 (s, 3H), 2.75 (t, 2H), 3.44 (q, 2H), 6.01 (d, 1 H), 6.05-6.07 (m, 1 H), 6.74 (d, 1H), 6.90-7.02 (m, 4H), 7.22 (d, 1H) , 7.29 (d, 1H); MS (ESI+): 479 ([M+H]+).

Example 256 Preparation of 1 -(4-{1 -Ethyl-1 -[3-methyl-(S)-4-(tetrahydro-furan-2-ylmethoxy)- phenyl]-propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol

OH Preparation of 5(S)-[4-(1 -{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pentyl]-3-methyl- phenyl}-1-ethyl-propyl)-2-methyl-phenoxymethyl]-dihydro-fura n- 2-one

0 OTBS y- OTBS

To a solution of 4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pen tyl]-3- methyl-phenyl}-1-ethyl- propyl)-2-methyl-phenol (compound prepared in Example 187-(1)) (140 mg, 0.28 mmol) in DMF (1.4 ml), (S)-(+)-dihydro-5-(p- tolylsulfonyloxymethyl)-2(3H)-furanone (228 mg, 0.84 mmol), and K2CO3 (195 mg, 1.41 mmol) were added at room temperature and the mixture was stirred at room temperature for 8 h. To the mixture, ethyl acetate was added and the mixture was washed with 30% NaH2PO4 aq. and brine, dried over MgSO4, concentrated in vacuo. The obtained residue was chromatographed on silica gel (AcOEt/hexane =1/2 to 2/1) to give the title compound (140 mg, 36%) as colorless oil. 1H-NMR (CDCI3): 0.07 (s, 3H),0.10 (s, 3H),0.59 (t, 6H1 J=7.3Hz),0.84 (s, 9H),0.93 (s, 9H),1.5-1.9 (m, 2H),2.04 (q, 4H, J=7.3Hz),2.16 (s, 3H),2.24 (s, 3H),2.32-2.48 (m, 4H),2.50-2.82 (m, 2H),3.34 (dd, 1 H, J=3.2, 7.2Hz),4.12 (ddd, 2H, J=3.5, 10.3, 13.7Hz),4.85-4.95 (m, 1 H),6.66 (d, 1 H, J=8.2Hz),6.85-7.00 (m, 5H);

(2) Preparation of tert-Butyl-{1-[2-(4-{1-ethyl-1-[3-methyl-(S)-4-(tetrahydro-f uran- 2-ylmethoxy)-phenyl]-propyl}-2-methyl-phenyl)-ethyl]-2,2-dim ethyl-propoxy}- dimethyl-silane

OTBS OH ' i OTBS OTBS

To a solution of 5(S)-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4)4-dimeth yl- pentyl]-3-methyl-phenyl}- 1 -ethyl-propyl)-2-methyl-phenoxymethyl]-dihydro-furan- 2-one (compound prepared in Example 256-(1))(62 mg, 0.1 mmol) in Et2θ (1 ml), LJAIH4 (6 mg, 0.16 mmol) was added at 0 degrees C and the mixture was stirred at room temperature for 2 h. To the mixture, ethyl acetate and brine were added and the mixture was stirred at room temperature for 0.5 h, dried over MgSO4, concentrated in vacuo to give 5-[4-(1-{4-[3-(tert-Butyl-dimethyl- silanyloxy)-4,4-dimethyl-pentyl]-3-methyl-phenyl}-1-ethyl-pr opyl)-2-methyl- phenoxy]-(4S)-pentane-1 ,4-diol (60mg) as colorless oil. To a solution of 5-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pentyl]- 3-methyl-phenyl} -1-ethyl-propyl)-2-methyl-phenoxy]-(4S)-pentane-1 ,4-diol (45 mg, 0.075mmol) in THF (0.5ml), PPh3 (20 mg, 0.076 mmol) and DEAD (0.014 ml, 0.077 mmol) were added at 0 degrees C and the mixture was stirred at room temperature for 2 h. To the mixture, Et2O was added and the mixture was washed with water and brine, dried over MgSO4, concentrated in vacuo. The obtained residue was chromatographed on silica gel (AcOEt/hexane =1/10) to give the title compound (22 mg, 50%) as colorless oil. 1H-NMR (CDCI3): 0.07 (s, 3H), 0.10 (s, 3H), 0.60 (t, 6H, J=7.3Hz), 0.88 (s, 9H), 0.93 (S, 9H), 1.50-1.60 (m, 1 H), 1.80-2.08 (m, 10H), 2.18 (s, 3H), 2.23 (s, 3H), 2.41 (dt, 1 H, J=4.5, 12.9Hz), 2.76 (dt, 1 H, J=5.6, 12.6Hz), 3.34 (dd, 1 H, J=3.2, 7.2Hz), 3.80-4.10 (m, 4H), 4.20-4.40 (m, 1H), 6.68 (d, 1H, J=8.1Hz), 6.91-6.99 (m, 5H).

(3) Preparation of 1-(4-{1 -Ethyl-1 -[3-methyl-(S)-4-(tetrahydro-furan-2-ylmethoxy)- phenyl]-propyl}-2-methyl-phenyl)-4,4-dimethyl-pentan-3-ol

OTBS V-O ' ' OH To a solution of tert-Butyl-{1 -[2-(4-{1 -ethyl-1 -[3-methyl-(S)-4-(tetrahydro-furan-2- ylmethoxy)-phenyl]-propyl}-2-methyl-phenyl)-ethyl]-2,2-dimet hyl-propoxy}- dimethyl-silane (compound prepared in Example 256-(2)) (20 mg, 0.034 mmol) in THF (1 ml), TBAF (1M in THF, 0.5 ml, 0.5 mmol) was added at room temperature and the mixture was refluxed for 3 h. To the mixture, Et2O was added and the mixture was washed with water, dried over MgSO4, concentrated in vacuo. The obtained residue was chromatographed on silica gel (AcOEt/hexane =1/2) to give the title compound (8 mg, 51%) as colorless oil. 1H-NMR (CDCI3): 0.59 (t, 6H, J=7.3Hz), 0.89 (s, 9H), 1.26 (t, 3H, J=7.2Hz), 1.30-1.60 (m, 1 H), 1.70-2.15 (m, 10H), 2.18 (s, 3H), 2.25 (s, 3H), 2.50-2.65 (m, 1 H), 2.80-2.90 (m, 1 H), 3.20-4.00 (m, 4H), 4.20-4.40 (m, 1 H), 6.68 (d, 1 H, J=8.2Hz), 6.90-6.95 (m, 4H), 7.02 (d, H, J=8.6Hz) ; MS (ESI+) : 484 ([M+NH4]+).

Example 257 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl} -2- methyl-phenoxy)-4-oxo-pentanoic acid

o (1) Preparation of 5-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pentyl]-3-methyl-phenyl} -1-ethyl-propyl)-2-methyl-phenoxy]-4(S)-hydroxy- pentanoic acid methyl ester

o- MeO- OTBS OTBS

To a solution of (S)-5-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimet hyl- pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxymet hyl]-dihydro-furan- 2-one (compound prepared in Example 256-(1)) (60 mg, 0.1 mmol) in THF (0.5 ml) and MeOH (1 ml), 1 N KOH aq. (0.2 ml, 0.2 mmol) was added at room temperature and the mixture was stirred at room temperature for 2 h. To the mixture, ethyl acetate was added and the mixture was washed with 30% NaHaPO4 aq. and brine, dried over MgSO4, concentrated in vacuo, and chromatographed on silica gel (AcOEt/hexane =1/2) to give carboxylic acid. To a solution of the carboxylic acid in toluene (0.5 ml) and MeOH (0.5 ml), TMSCHN2 (1M in Et2O) was added at room temperature and the mixture was stirred at room temperature for 2 h. The reaction mixture was concentrated in vacuo and the obtained residue was chromatographed on silica gel (AcOEt/hexane =1/2) to give the title compound (60 mg, 95%) as colorless oil. 1H-NMR (CDCI3): 0.07 (s, 3H), 0.11 (s, 3H), 0.61 (t, 6H, J=7.2Hz), 0.89 (s, 9H), 0.94 (s, 9H), 1.50-1.65 (m, 1H), 1.70-1.96 (m, 3H), 2.02 (q, 4H, J=7.1Hz), 2.18 (s, 3H), 2.24 (s, 3H), 2.30-2.60 (m, 3H), 2.70-2.85 (m, 1H), 3.30-3.40 (m, 1H), 3.70 (s, 3H), 3.80-4.10 (m, 2H), 4.10 (brs, 1H), 6.68 (d, 1H, J=8.1Hz), 6.90-7.10 (m, 5H);

(2) Preparation of 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-4-oxo-pentanoic acid OTBS O ' I OH

To a solution of 5-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxy]-4 (S)-hydroxy- pentanoic acid methyl ester (compound prepared in Example 257-(1))(60 mg, 0.1 mmol) in dichloromethane (1 ml), Dess-Martin reagent (50 mg, 0.12 mmol) was added at 0 degrees C and the mixture was stirred at room temperature for 1 h. To the mixture, ethyl acetate was added and the mixture was washed with saturated NaHCO3 aq., water, and brine, dried over MgSO4, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (AcOEt/hexane =1/2) to give 5-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4- dimethyl-pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-p henoxy]-4-oxo- pentanoic acid methyl ester (58mg, 97%) as colorless oil. To a solution of 5-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pentyl]- 3-methyl-phenyl} -1 -ethyl-propyl)-2-methyl-phenoxy]-4-oxo-pentanoic acid methyl ester (58 mg, 0.1 mmol) in THF (1ml), TBAF (1 M in THF, 1 ml, 1 mmol) was added at 0 degrees C and the mixture was refluxed for 4 h. To the mixture, ethyl acetate was added and the mixture was washed with 30% NaH2PO4 aq., dried over MgSO4, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (AcOEt/hexane =5/1) to give the title compound (11 mg, 23%) as colorless oil. 1H-NMR (CDCI3): 0.59 (t, 6H, J=7.3Hz), 0.89 (s, 9H), 1.40-1.60 (m, 1H), 1.70- 1.90 (m, 1H), 2.04 (q, 4H, J=7.1Hz), 2.24 (s, 3H), 2.25 (s, 3H), 2.50-2.61 (m, 1 H), 2.71 (t, 2H, J=6.4Hz), 2.80-3.30 (m, 3H), 4.12 (dd, 1 H, J=7.2, 14.3Hz), 4.52 (brs, 2H), 6.56 (d, 1 H, J=9.1 Hz), 6.80-7.10 (m, 5H); MS (ESI+) : 519 ([M+Na]+).

Example 258 Preparation of 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-pentane-1 ,4-diol Preparation of 5-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxy)-(4S)-pentane-1 ,4-diol

OH

To a solution of 5(S)-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimeth yl- pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxymet hyl]-dihydro-furan- 2-one (compound prepared in Example 256-(1)) (62 mg, 0.1 mmol) in Et2O (1 ml), LJAIH4 (6 mg, 0.16 mmol) was added at 0 degrees C and the mixture was stirred at room temperature for 2 h. To the mixture, ethyl acetate and brine were added and the mixture was stirred at room temperature for 0.5 h, dried over MgSO4, concentrated in vacuo to give 5-[4-(1-{4-[3-(tert-Butyl-dimethyl- silanyloxy)-4,4-dimethyl-pentyl]-3-methyl-phenyl}-1-ethyl-pr opyl)-2-methyl- phenoxy]-(4S)-pentane-1 ,4-diol (60 mg) as colorless oil. To a solution of 5-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pentyl]- 3-methyl-phenyl} -1-ethyl-propyl)-2-methyl-phenoxy]-(4S)-pentane-1 ,4-diol (15 mg, 0.075mmol) in THF (1 ml), TBAF (1M in THF, 1 mmol) was added at room temperature and the mixture was refluxed for 4 h. To the mixture, ethyl acetate was added and the mixture was washed with 30% NaH2PO4 aq., dried over MgSO4, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (AcOEt/hexane =5/1) to give the title compound (11 mg, 90%) as colorless oil. 1H-NMR (CDCI3): 0.60 (t, 6H, J=7.3Hz), 0.93 (s, 9H), 1.40-1.90 (m, 6H), 2.04 (q, 4H, J=7.4Hz), 2.18 (s, 3H), 2.26 (s, 3H), 2.50-2.65 (m, 1H), 2.80-2.95 (m, 1H), 3.25 (dd, 1H, J=1.6, 10.4Hz), 3.65-3.80 (m, 2H), 3.84 (dd, 1H, J=7.4, 9.2Hz), 3.96 (dd, 1H1 J=3.6, 9.1Hz), 4.00-4.15 (m, 1H), 6.68 (d, 1H, J=8.2Hz), 6.85-7.00 (m, 4H), 7.02 (d, 1H, J=8.7Hz); MS (ESI+) : 485 ([M+H]+).

Example 259 Preparation of 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenyl)-hex-5-ynoic acid

HOOC

(1) Preparation of Trifluoro-methanesulfonic acid 4-(1-{4-[3-(tert-butyl-dimethyl- silanyloxy)-4,4-dimethyl-pentyl]-3-methyl-phenyl}-1-ethyl-pr opyl)-2-nnethyl-phenyl ester

HO" ^T I ^TI ^ ΥI " ^ Tf0' I l OTBS ' ' OTBS To a solution of 4-(1 -{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl-pentyl] -3- methyl-phenyl}-1-ethyl-propyl)-2-methyl- phenol (compound prepared in Example 187-(1)) (1.8 g, 3.6 mmol) in dichloromethane (18 ml), pyridine (0.44 ml, 5.4 mmol), and Tf2O (0.73 ml, 4.3 mmol) were added at 0 degrees C and the mixture was stirred at room temperature for 0.5 h. To the mixture, ethyl acetate was added and the mixture was washed with water, dried over MgSO4, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (ethyl acetate/hexane =1/10) to give the title compound (1.55 g, 68%) as colorless oil. 1H-NMR (CDCI3): 0.06 (s, 3H), 0.09 (s, 3H), 0.59 (t, 6H, J=7.3Hz), 0.87 (s, 9H), 0.93 (s, 9H), 1.50-1.65 (m, 1 H), 1.70-1.85 (m, 1 H), 2.04 (q, 4H, J=7.3Hz), 2.23 (s, 3H)1 2.31 (s, 3H), 2.41 (dt, 1H1 J=4.5, 13.0Hz), 2.76 (dt, 1H, J=5.5, 13.0Hz), 3.34 (dd, 1 H, J=3.3, 7.0Hz), 6.80>6.90 (m, 2H), 6.95-7.15 (m, 4H).

(2) Preparation of Trifluoro-methanesulfonic acid 4-{1-ethyl-1-[4-(3-hydroxy-4,4- dimethyl-pentyl)-3-methyl-phenyl]-propyl}-2-methyl-phenyl ester

TfO TfO OTBS To a solution of trifluoro-methanesulfonic acid 4-(1-{4-[3-(tert-butyl-dimethyl- silanyloxy)-4,4-dimethyl-pentyl]-3-methyl-phenyl}-1-ethyl-pr opyl)-2-methyl-phenyl ester (compound prepared in Example 259-(1 )) (95 mg, 0.15 mmol) in dichloromethane (0.75 ml), trifluoroacetic acid (0.25 ml) was added at room temperature and the mixture was stirred at room temperature for 1.5 h. The mixture was concentrated in vacuo, and chromatographed on silica gel (ethyl acetate/hexane =1/2) to give the title compound (70 mg, 90%) as colorless oil. 1H-NMR (CDCI3): 0.60 (t, 6H, J=7.3Hz), 0.90 (s, 9H), 1.35-1.60 (m, 2H), 1.70- 1.90 (m, 1 H), 2.06 (q, 4H, J=7.3Hz), 2.27 (s, 3H), 2.32 (s, 3H), 2.50-2.65 (m, 1H), 2.80-3.00 (m, 1H), 3.26 (brd, 1 H, J=10.2Hz), 6.80-6.95 (m, 2H), 7.00-7.20 (m, 4H);

(3) Preparation of 6-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenyl)-hex-5-ynoic acid

TfO- MeOOC. HOOC

To a solution of trifluoro-methanesulfonic acid 4-(1-{4-[3-(tert-butyl-dimethyl- silanyloxy)-4,4-dimethyl-pentyl]-3-methyl-phenyl}-1-ethyl-pr opyl)-2-methyl-phenyl ester (compound prepared in Example 259-(2)) (50 mg, 0.1 mmol) in DMF (1 ml), PdCI2(dppf)2-CH2Cl2 (8 mg, 0.01 mmol), Et3N (0.05 ml, 0.3 mmol), CuI (20 mg, 0.1 mmol), and hex-5-ynoic acid methyl ester (20 mg, 0.16 mmol) were added at room temperature under nitrogen and stirred at 120 degrees C for 8 h. To the mixture, ethyl acetate was added and the mixture was washed with water and brine, dried over MgSO4, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (ethyl acetate/hexane =1/4) to give 6-(4-{1- ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]- propyl}-2-methyl- phenyl)-hex-5-ynoic acid methyl ester (16mg) as colorless oil including impurities. To a solution of 6-(4-{1-ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenyl)-hex-5-ynoic acid methyl ester(16 mg) in MeOH (1 ml), 1 N NaOH aq. (0.2 ml, 0.2 mmol) was added at room temperature and stirred at room temperature for 4 h. To the mixture, ethyl acetate was added and the mixture was washed with 30% NaH2PO4 aq., dried over MgSO4, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (ethyl acetate/hexane =1/1) to give the title compound (6 mg, 13%, 2steps) as colorless oil. 1H-NMR (CDCI3): 0.59 (t, 6H1 J=7.3Hz), 0.89 (s, 9H), 1.40-1.60 (m, 1H), 1.70- 2.00 (m, 3H), 2.05 (q, 4H, J=7.3Hz), 2.24 (s, 3H), 2.35 (s, 3H), 2.45-2.65 (m, 5H), 2.80-2.95 (m, 1 H), 3.24 (dd, 1 H, J=1.5, 10.4Hz), 6.80-7.05 (m, 5H), 7.23 (d, 1 H, J=8.1Hz); MS (ESI+) : 494 ([M+NH4]+).

Example 260 Preparation of (R)-5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1 -methyl-cyclohexyl)-prop-1 - ynyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dihyd ro-furan-2-one

OH

(1) Preparation of 1 -Methyl-cyclohexanecarboxylic acid N-methoxy-N-methyl- amide HO^ "► sO.

To a solution of 1-Methyl-i-cyclohexanecarboxylic acid (500 mg, 3.516 mmol) in CH2CI2 (5 ml), methoxymethyl amine hydrochloride (411.6 mg, 4.219 mmol), DMAP (214.8 mg, 1.758 mmol), Et3N (996.2 mg, 9.845 mmol) and HCI salt of WSCI (943.7 mg, 4.923 mmol) were added under nitrogen gas at 0 degrees C and the mixture was stirred at room temperature for 17 h. To the mixture, ethyl acetate was added and the organic layer was washed with brine, dried over magnesium sulfate, concentrated in vacuo and the obtained residue was chromatographed on silica gel (dichrolomethane/methanol =90/10) to give the title compound (373.5 mg, 57.3%). 1H-NMR (chloroform-d): 1.17 (s, 3H), 1.24-1.56 (m, 8H), 2.05-2.11 (m, 2H), 3.15 (s, 3H), 3.64 (s, 3H); MS (ESI+) : 186([M+H]+).

(2) Preparation of tert-Butyl-{4-[1-ethyl-1-(4-ethynyl-3-methyl-phenyl)-propyl] -2- methyl-phenoxy}-dimethyl-silane

^? TBSO To a solution of 4-[1-Ethyl-1-(4-ethynyl-3-methyl-phenyl)-propyl]-2-methyl- phenol (compound prepared in Example 1-(3)) (639 mg, 2.185 mmol) in DMF (2.7 ml), TBSCI (658.8 mg, 4.371 mmol) and imidazole (743.9 mg, 10.926 mmol) were added at room temperature and the mixture was stirred at room temperature for 17 h. To the mixture, ethyl acetate was added and the mixture was washed with water and brine, dried over magnesium sulfate, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (n- hexane/ethyl acetate =97/3 to ethyl acetate=only) to give the title compound (555.2 mg, 62.5%) as colorless oil. 1H-NMR (chloroform-d): 0.23 (s, 6H), 0.62 (t, 6H, J=7.3Hz), 1.03 (s, 9H), 2.06 (q, 4H, J=7.3Hz), 2.18 (s, 3H), 2.42 (s, 3H), 3.23 (s, 1H), 6.67 (d, 1H, J=8.4Hz), 6.84 (dd, 1 H, J=2.6, 8.4Hz), 6.90 (d, 1H, J=2.4Hz), 6.97 (dd, 1 H, J=2.0, 8.1Hz), 7.04 (brs, 1H), 7.36 (d, 1H1 J=8.2Hz); MS (ESI+) : 407([M+H]+).

(3) Preparation of 3-(4-{1-[4-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenyl)-1 -(1 -methyl-cyclohexyO-prop^-yn-i -one

TBSO TBSO ^?

To a solution of tert-Butyl-{4-[1-ethyl-1-(4-ethynyl-3-methyl-phenyl)-propyl] -2~ methyl-phenoxy}-dimethyl-silane (compound prepared in Example 260-(2)) (50 mg, 0.123 mmol) in THF (0.2 ml), n-BuLi in n-hexane (0.07 ml, 0.172 mmol) was added at -78 degrees C under nitrogen gas and the mixture was stirred at room temperature for 20 min. And then, to this solution, 1-methyl- cyclohexanecarboxylic acid methoxy-methyl-amide (compound prepared in Example 260-(1)) (34.2 mg, 0.185 mmol) was added at -78 degrees C under nitrogen gas and the mixture was stirred for 15 h raising the reaction temperature from -78 degrees C to room temperature. To the mixture, ethyl acetate was added and the mixture was washed with saturated ammonium chloride solution and brine, dried over magnesium sulfate, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (n- hexane/ethyl acetate =10/1) to give the title compound (41.1 mg, 62.9%). MS (ESI+) : 531([M+H]+).

(4) Preparation of 3-(4-{1-[4-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenyl)-1 -(1-methyl-cyclohexyl)-prop-2-yn-1-ol

TBSO

To a solution of 3-(4-{1 -[4-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-phenyl]-1 - ethyl-propyl}-2-methyl-phenyl)-1-(1-methyl-cyclohexyO-prop^- yn-i -one (compound prepared in Example 260-(3)) (41.1 mg, 0.077 mmol) in THF (0.8 ml) and MeOH (0.3 ml), NaBH4 (8.8 mg, 0.232 mmol) was added at room temperature and stirred at room temperature for 13 h. To the mixture, ethyl acetate was added and the mixture was washed with brine, dried over magnesium sulfate, concentrated in vacuo, and chromatographed on silica gel (n-hexane/ethyl acetate =30/1) to give the title compound (36.5 mg, 88.5%). 1H-NMR (chloroform-d): 0.21 (s, 6H), 0.60 (t, 6H, J=7.4Hz), 1.02 (s, 9H), 1.08 (s, 3H), 1.40-1.63 (m, 10H), 1.77 (brs, 1H), 2.04 (q, 4H, J=7.4Hz), 2.15 (s, 3H), 2.39 (s, 3H), 4.35 (s, 1H), 6.63 (d, 1H, J=8.2Hz), 6.81 (dd, 1H, J=2.5, 8.3Hz), 6.86 (d, 1 H, J=2.3Hz), 6.94 (dd, 1 H, J=1.6, 8.1 Hz), 7.00 (brs, 1 H), 7.29 (d, 1H, J=8.2Hz).

(5) Preparation of (R)-5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclohexyl)-pr op- 1-ynyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dih ydro-furan-2-one

TBSO OH O' OH To a solution of 3-(4-{1-[4-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenyl)-1 -(1-methyl-cyclohexyl)-prop-2-yn-1-ol (compound prepared in Example 260-(4)) (36 mg, 0.068 mmol) in THF (0.7 ml), 1.0M TBAF in THF (0.1 ml, 0.1 mmol) was added at room temperature and stirred at room temperature for 15 h. To the mixture, ethyl acetate was added and the mixture was washed with diluted potassium hydrogen sulfate aq. and brine, dried over magnesium sulfate, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (n-hexane/ethyl acetate =10/1 and 7/1) to give the mixture including the title compound (28.8 mg). To a solution of this mixture (10 mg) in DMF (0.2 ml), (R)-(-)-Dihydro-5-(p-tolyl- sulfonyloxymethyl)-2(3H)-furanone (16.1 mg, 0.06 mmol) and K2CO3 (13.2 mg, 0.096 mmol) were added at room temperature and stirred at 105 degrees C for 11 h. To the reaction mixture, ethyl acetate was added and the mixture was washed with brine, dried over magnesium sulfate, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (n-hexane/ethyl acetate =3/1) to give the title compound (4.6 mg, 37.3% for 2 steps). 1H-NMR (chloroform-d): 0.59 (t, 6H, J=7.3Hz), 1.07 (s, 3H), 1.40-1.64 (m, 10H), 1.74 (d, 1H, J=6.2Hz), 2.04 (q, 4H, J=7.3Hz), 2.15 (s, 3H), 2.26-2.63 (m, 3H), 2.39 (s, 3H), 2.78 (ddd, 1H, J=6.8, 9.7, 17.0Hz), 4.06 (dd, 1H, J=3.5, 10.3Hz), 4.17 (dd, 1H, J=3.3, 10.3Hz), 4.35 (d, 1H, J=6.3Hz), 4.86-4.92 (m, 1H), 6.66 (d, 1H, J=8.5Hz), 6.87 (brd, 1H, J=1.8Hz), 6.90-6.95 (m, 2H), 6.98 (brs, 1H), 7.29 (d, 1H, J=8.1 Hz); MS (ESI+) : 534([M+NH4∏.

Example 261 Preparation of (R)-5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1 -methyl-cyclohexyl)-propyl]- 3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dihydro-fur an-2-one

OH

(1) Preparation of 4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclohexyl)-propyl]-3 - methyl-phenyl}-propyl)-2-methyl-phenol

To a solution of 4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclohexyl)-prop-1-yn yl]- 3-methyl-phenyl}-propyl)-2-methyl-phenol (compound prepared in Example 260- (5)) (18 mg, 0.043 mmol) in AcOEt (1 ml), 10% Pd-C (2 mg) was added and the mixture was stirred at room temperature under hydrogen gas for 15 h. To the mixture, ethyl acetate was added and the mixture was filtered through celite, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (n-hexane/ethyl acetate =3/1 and 1/1) to give the title compound (15.5 mg, 85.3%). 1H-NMR (chloroform-d): 0.60 (t, 6H1 J=7.5Hz), 0.85 (s, 3H), 1.23-1.59 (m, 12H), 1.75-1.84 (m, 1 H), 2.04 (q, 4H, J=7.5Hz), 2.20 (s, 3H)1 2.26 (s, 3H), 2.56 (ddd, 1H, J=6.3, 10.0, 13.9Hz), 2.88 (ddd, 1 H, J=5.0, 10.1 , 15.1 Hz), 3.32 (brd, 1 H, J=10.0Hz), 4.71 (brs, 1H), 6.65 (d, 1H, J=8.2Hz), 6.84-6.92 (m, 4H), 7.02 (d, 1H, J=8.6Hz); MS(positive): 440([M+NH4]+).

(2) Preparation of (R)-5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclohexyl)- propyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dih ydro-furan-2-one

OH

To a solution of 4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclohexyl)-propyl]-3 - methyl-phenyl}-propyl)-2-methyl-phenol (compound prepared in Example 261- (1)) (15 mg, 0.035 mmol) in DMF (0.4 ml), toluene-4-sulfonic acid (R)-5-oxo- tetrahydro-furan-2-ylmethyl ester (24 mg, 0.089 mmol) and K2CO3 (19.6 mg, 0.142 mmol) was added at room temperature and the mixture was stirred at 60 degrees C for 4 h and at 85 degrees C for 4 h. To the mixture, ethyl acetate was added and the mixture was washed with water and brine, dried over magnesium sulfate, concentrated in vacuo and the obtained residue was chromatographed on silica gel (n-hexane/ethyl acetate =3/1 and 1/1) to give the title compound (9.3 mg, 50.4%). 1H-NMR (chloroform-d): 0.60 (t, 6H, J=7.3Hz), 0.85 (s, 3H), 1.16-1.65 (m, 11 H), 1.73-1.87 (m, 1 H), 2.04 (q, 4H, J=7.3Hz), 2.16 (s, 3H), 2.18 (s, 3H), 2.26-2.63 (m, 4H), 2.73-2.92 (m, 2H), 3.28-3.33 (m, 1 H), 4.07 (dd, 1 H, J=3.5, 10.3Hz), 4.17 (dd, 1H, J=3.4, 10.3Hz), 4.86-4.92 (m, 1H), 6.66 (d, 1H, J=8.3Hz), 6.89-7.03 (m, 5H); MS (ESI+) : 538 ([M+NH4]+).

Example 262 Preparation of (R)-5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclohexyl)-pr op-1 - ynyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-p entanoic acid OH H

Preparation of (R)-5-[4-(1 -Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclohexyl)-prop-1 - yny∏-S-methyl-phenylJ-propyO^-methyl-phenoxyH-hydroxy-pent anoic acid

O OH OH To a solution of δ-^i-Ethyl-i-^-β-hydroxy-S^I-methyl-cyclohexyO-prop-i- ynyll-S-methyl-phenylJ-propyO^-methyl-phenoxymethylJ-dihydro -furan^-one (compound prepared in Example 260-(5)) (4 mg, 0.008 mmol) in THF (0.15 ml) and MeOH (0.05 ml), 1N KOH aq (0.05 ml, 0.05 mmol) was added at room temperature and the mixture was stirred at 65-70 degrees C for 2 h. The mixture was concentrated in vacuo and chromatographed on silica gel (dichloromethane/methanol =10/1) to give the title compound (2.1 mg, 50.7%). 1H-NMR (chloroform-d): 0.60 (t, 6H, J=7.3Hz), 1.07 (s, 3H), 1.40-1.68 (m, 10H), 1.89-2.02 (m, 2H), 2.04 (q, 4H, J=7.3Hz), 2.16 (s, 3H), 2.39 (s, 3H), 2.63 (t, 2H, J=7.2Hz), 3.85 (dd, 1H, J=6.9, 9.2Hz), 3.97 (dd, 1H, J=3.5, 9.2Hz), 4.02-4.16 (m, 1H), 4.35 (s, 1H), 6.67 (d, 1H, J=8.4Hz), 6.87-6.99 (m, 4H), 7.29 (d, 1H, J=8.1Hz); MS (ESI-) : 533([M-H]").

Example 263 Preparation of (R)-5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1-methyl-cyclohexyl)-propyl]- 3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentano ic acid

O

OH Preparation of (R)-5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1 -methyl-cyclohexyl)-propyl]- S-methyl-phenylJ-propyO^-methyl-phenoxyH-hydroxy-pentanoic acid

OH

To a solution of δ-K-O-Ethyl-i-^-tS-hydroxy-S-O-methyl-cyclohexyO-propyll-S- methyl-phenylJ-propyO^-methyl-phenoxymethyll-dihydro-furan^- one (compound prepared in Example 261) (8.7 mg, 0.017 mmol) in THF (0.3 ml) and MeOH (0.1 ml), 1 N KOH aq (0.1 ml, 0.1 mmol) was added at room temperature and the mixture was stirred at 65-70 degrees C for 2 h. The mixture was concentrated in vacuo and chromatographed on silica gel (dichloromethane/methanol =10/1) to give the title compound (3.7 mg, 41.1%). 1H-NMR (chloroform-d): 0.60 (t, 6H, J=7.2Hz), 0.85 (s, 3H), 1.15-1.59 (m, 11 H), 1.74-1.84 (m, 1 H), 1.89-1.99 (m, 2H), 2.04 (q, 4H, J=7.3Hz), 2.17 (s, 3H), 2.26 (s, 3H), 2.51-2.60 (m, 1 H), 2.62 (dt, 2H, J=1.6, 7.1 Hz), 2.87 (ddd, 1H, J=4.8, 10.1, 13.9Hz)1 3.31 (brd, 1H, J=9.1Hz), 3.85 (dd, 1H, J=6.7, 9.2Hz), 3.98 (dd, 1 H, J=3.5, 9.2Hz), 4.04-4.11 (m, 1 H), 6.67 (d, 1 H, J=8.2Hz), 6.89-6.97 (m, 4H), 7.02 (d, 1 H, J=8.6Hz); MS (ESI-) : 537([M-H∏.

Example 264 Preparation of 4-(4-{1 -Ethyl-1 -[4-((S)-3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenoxymethyl)-benzoic acid

OH

(1) Preparation of 4-[4-(1-{4-[(S)-3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimet hyl- pentyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenoxymet hyl]-benzoic acid methyl ester MeO OTBS OTBS

To a solution of 4-(1-{4-[(S)-3-(tert!Butyl-dimethyl-silanyloxy)-4,4-dimethyl - pentyll-S-methyl-phenyty-i÷ethyl-propyl^-methyl-phenol (compound prepared in Example 187-(1)) (45 mg, 0.091 mmol) in DMF (0.9 ml), methyl 4- (bromomethyl)benzoate (52 mg, 0.226 mmol) and K2CO3 (50 mg, 0.362 mmol) were added at room temperature and the mixture was stirred at 110 degrees C for 13 h. To the mixture, ethyl acetate was added and the mixture was washed with brine, dried over magnesium sulfate, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (n-hexane/ethyl acetate =10/1) to give the title compound (33.6 mg, 57.5%). 1H-NMR (chloroform-d): 0.08 (s, 3H), 0.12 (s, 3H), 0.62 (t, 6H, J=7.3Hz), 0.89 (s, 9H), 0.95 (s, 9H), 1.52-1.65 (m, 1 H), 1.74-1.85 (m, 1 H), 2.06 (q, 4H, J=7.3Hz), 2.25 (s, 6H), 2.43 (dt, 1 H, J=4.7, 12.3Hz), 2.77 (dt, 1H, J=5.3, 13.6Hz), 3.35 (dd, 1H, J=3.2, 7.2Hz), 3.93 (s, 3H), 5.10 (s, 2H), 6.74 (d, 1H, J=8.8Hz), 6.91-7.01 (m, 5H), 7.52 (d, 2H, J=8.6Hz), 8.06 (d, 2H, J=8.4Hz).

(2) Preparation of 4-(4-{1-Ethyl-1-[4-((S)-3-hydroxy-4,4-dimethyl-pentyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-benzoic acid

MeO OH

To a solution of 4-[4-(1-{4-[(S)-3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimet hyl- pentylj-S-methyl-phenylJ-i-ethyl-propyl^-methyl-phenoxymethy ll-benzoic acid methyl ester (compound prepared in Example 264-(1)) (33.6 mg, 0.052 mmol) in THF (0.5 ml), 1.0M TBAF in THF (0.26 ml, 0.26 mmol) was added at room temperature and the mixture was stirred at 70 degrees C for 4 h. To the mixture, ethyl acetate was added and the mixture was washed with diluted potassium hydrogen sulfate aq. and brine, dried over magnesium sulfate, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (dichloromethane/methanol =10/1 and dichloromethane/methanol =15/1) to give the title compound (16.5 mg, 61.3%). 1H-NMR (chloroform-d): 0.61 (t, 6H, J=7.3Hz), 0.90 (s, 9H), 1.45-1.58 (m, 1 H)1 1.76-1.85 (m, 1 H), 2.05 (q, 4H, J=7.3Hz), 2.25 (s, 3H), 2.26 (s, 3H), 2.56 (ddd, 1H, J=6.0, 10.1 , 14.1Hz), 2.88 (ddd, 1H, J=5.1 , 10.7, 14.1Hz), 3.26 (dd, 1H, J=1.5Hz), 5.12 (s, 2H), 6.74 (d, 1 H, J=9.1 Hz), 6.91-6.97 (m, 4H), 7.03 (d, 1 H, J=7.9Hz), 7.56 (d, 2H, J=8.2Hz), 8.13 (d, 2H, J=8.2Hz); MS (ESI-) : 515([M-H]").

Example 265 Preparation of 4-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1 -ynyl)-3-methyl- phenyl]-propyl}-2-methyl-phenylcarbamoyl)-butyric acid

HOOC

(1 ) Preparation of 3-m-Tolyl-pentan-3-ol

COOMe

To a solution of 3-Methyl-benzoic acid methyl ester (5 g, 33.29 mmol) in THF (50 ml) at 0 degrees C was added EtMgBr (3M in Et2θ, 33 ml) and the mixture was stirred at 0 degrees C for 1 h. The reaction mixture was poured into sat. NH4CI aq. and the products were extacted with AcOEt. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to give the title compound (5.67 g, 96%). 1H NMR (CDCI3): 0.76 (6H, t, J = 7.59 Hz), 1.75-1.90 (4H, m), 2.36 (3H, s), 7.03 (1 H, d, J = 7.42 Hz), 7.12-7.26 (3H, m)

(2) Preparation of 4-(1-Ethyl-1-m-tolyl-propyl)-2-methyl-phenol To a solution of 3-m-Tolyl-pentan-3-ol (5.57 g, 31 24 mmol) (compound prepared in Example 265-(1))in toluene (50 ml) were added cresol (12.5 ml, 93.73 mmol) and AICI3 (4.58 g, 34.36 mmol) and the mixture was stirred at room temperature overnight. The reaction mixture was poured into 1 N-HCI and the products were extacted with CH2CI2. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with CH2CI2 to give the title compound (8 g, 95%) as colorless oil. 1H NMR (CDCI3): 0.60 (6H, t, J = 7.26 Hz), 2.00-2.09 (4H, q, J = 7.25 Hz), 2.19 (3H1 s), 2.29 (3H, s), 4.57 (1H1 s), 6.63-7.13 (7H, m)

(3) Preparation of Trifluoro-methanesulfonic acid 4-(1-ethyl-1-m-tolyl-propyl)-2- methyl-phenyl ester

OTf

To a solution of 4-(1-Ethyl-1-m-tolyl-propyl)-2~methyl-phenol (compound prepared in Example 265-(2)) (400mg, 1.490 mmol) were added Tf2O (0.276 ml, 1.639 mmol) and Et3N (0.310 ml, 2.235 mmol) and the mixture was stirred at room temperature for 30 min. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extacted with CH2CI2. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n- Hexane-AcOEt (1:1) to give the title compound (412 mg, 69%) as colorless oil. 1H NMR (CDCI3): 0.60 (6H, t, J = 7.25 Hz), 2.07 (4H, q, J = 7.42 Hz), 2.30 (3H, s), 2.32 (3H, s), 6.92-7.18 (7H, m) (4) Preparation of Trifluoro-methanesulfonic acid 4-[1 -ethyl-1 -(3-methyl-4-nitro- phenyl)-propyl]-2-methyl-phenyl ester

OTf OTf

To a solution of Trifluoro-methanesulfonic acid 4-(1 -ethyl-1 -m-tolyl-propyl)-2- methyl-phenyl ester (compound prepared in Example 265-(3)) (100 mg, 0.250 mmol) in MeCN (3 ml) at 0 degrees C was added NO2BF4 (40 mg, 0.300 mmol) and the mixture was stirred at 0 degrees C for 15 min. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extacted with CH2CI2. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane-AcOEt (10:1) to give the title compound (42.2 mg, 38%) as colorless oil. 1H NMR (CDCI3): 0.62 (6H1 1, J = 7.42 Hz), 2.11 (4H, q, J = 7.42 Hz), 2.33 (3H, s), 2.58 (3H, s), 6.98-7.18 (5H, m), 7.91 (1 H, d, J = 9.06 Hz)

(5) Preparation of Trifluoro-methanesulfonic acid 4-[1-(4-amino-3-methyl- phenyl)-1 -ethyl-propyl]-2-methyl-phenyl ester

OTf OTf

To a solution of Trifluoro-methanesulfonic acid 4-[1-ethyl-1-(3-methyl-4-nitro- phenyl)-propyl]-2-methyl-phenyl ester (compound prepared in Example 265-(4)) (130 mg, 0.292 mmol) in MeOH (3 ml) was added Pd/C (10%, 20 mg) and the mixture was stirred at room temperature under H2 atmosphere for 1.5 h. The mixture was filtered through celite and concentrated under reduced pressure to give the title compound (113.2 mg, 93%). 1H NMR (CDCI3): 0.59 (6H, t, J = 7.25 Hz), 2.02 (4H, q, J = 7.42 Hz), 2.12 (3H, s), 2.31 (3H, s), 6.58 (1 H, d, J = 8.91 Hz), 6.77-6.83 (2H, m), 7.04-7.12 (3H1 m) (6) Preparation of 4-{4-[1-Ethyl-1-(3-methyl-4-trifluoromethanesulfonyloxy- phenyl)-propyl]-2-methyl-phenylcarbamoyl}-butyric acid methyl ester

MeOOC. OTf VN ^T Y OTf

To a solution of Trifluoro-methanesulfonic acid 4-[1-(4-amino-3-methyl-phenyl)-1- ethyl-propyl]-2-methyl-phenyl ester (compound prepared in Example 265-(5)) (113 mg, 0.272 mmol) in CH2Cb (3 ml) were added glutaric acid mono methyl ester (60 mg, 0.409 mmol), EDC (104 mg, 0.544 mmol) and Et3N (0.113 ml, 0.816 mmol) and the mixture was stirred at room temperature overnight. The reaction mixture was poured into sat. NaHCU3 aq. and the products were extacted with CH2CI2. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane-AcOEt (1 :1) to give the title compound (111.5 mg, 75%) as colorless oil. 1H NMR (CDCI3): 0.60 (6H, t, J = 7.25 Hz)1 2.00-2.15 (6H, m), 2.21 (3H, s), 2.31 (3H, s), 2.41-2.50 (4H, m), 3.69 (3H, s), 6.91 (1 H, s), 6.97-7.15 (5H, m), 7.74 (1 H1 d, J = 8.41 Hz)

(7) Preparation of tert-Butyl-(1 -tert-butyl-prop-2-ynyloxy)-dimethyl-silane <% OH OTBS

To a solution of 4,4-Dimethyl-pent-1-yn-3-ol (J. Org. Chem. 53; 20; 1988; 4736- 4745) (360 mg, 3.209 mmol) in CH2CI2 (10 ml) were added TBSOTf (0.884 ml, 3.851 mmol) and imidazole (437 mg, 6.418 mmol) and the mixture was stirred at room temperature for 30 min. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extacted with CH2CI2. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n- Hexane-AcOEt (7:3) to give the title compound (314 mg, 43%) as colorless oil. 1H NMR (CDCI3): 0.02 (3H, s), 0.09 (3H, s), 0.91 (9H, s), 0.95 (9H, s), 2.34 (1H, s), 3.95 (1 H, s)

(8) Preparation of 4-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pent- 1 -ynyl]-3-methyl-phenyl}-1 -ethyl-propyl)-2-methyl-phenylcarbamoyl]-butyric acid methyl ester

MeOOC. ^ Λ,..sK^> ^^OTf " Mβ00C H I I ^ OTBS

To a solution of 4-{4-[1-Ethyl-1-(3-methyl-4-trifluoromethanesulfonyloxy-phen yl)- propyl]-2-methyl-phenylcarbamoyl}-butyric acid methyl ester (compound prepared in Example 265-(6)) (111 mg, 0.204 mmol) in DMF (3 ml) were added tert-Butyl-(1-tert-butyl-prop-2-ynyloxy)-dimethyl-silane (compound prepared in Example 265-(7)) (92 mg, 0.408 mmol), PdCI2(dppf)-CH2CI2 (18 mg, 0.022 mmol), CuI (7.8 mg, 0.041 mmol) and Et3N (0.085 ml, 0.612 mmol) and the mixture was stirred under nitrogen atmosphere at 100 degrees C overnight. The reaction mixture was poured into sat. NH4CI aq. and the products were extacted with AcOEt. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with n-Hexane-AcOEt (1:1) to give the title compound (50 mg, 40%) as colorless oil. 1H NMR (CDCI3): 0.10 (3H, s), 0.12 (3H, s), 0.60 (6H, t, J = 7.26 Hz), 0.93 (9H, s), 1.01 (9H, s), 2.00-2.13 (6H, m), 2.20 (3H, s), 2.36 (3H, s), 2.42-2.50 (4H, m), 3.69 (3H, s), 6.90-7.07 (5H, m), 7.25 (1 H, d, J = 7.92 Hz), 7.71 (1 H, d, J = 8.24 Hz)

(9) Preparation of 4-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pent- 1 -ynyl]-3-methyl-phenyl}-1 -ethyl-propyl)-2-methyl-phenylcarbamoyl]-butyric acid and 4-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3-methyl-phenyl]- propyl}-2-methyl-phenylcarbamoyl)-butyric acid

MeOOC. HOOC

OTBS

HOOC

To a solution of 4-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pent-1- ynylJ-S-methyl-phenylJ-i-ethyl-propyO^-methyl-phenylcarbamoy lJ-butyric acid methyl ester (compound prepared in Example 265-(8)) (50 mg, 0.081 mmol) in THF-H2O (10:1 , 3.3 ml) was added CSA (56 mg, 0.243 mmol) and the mixture was stirred at 70 degrees C for 6 h. The reaction mixture was poured into sat. NaHCO3 aq. and the products were extacted with CH2CI2. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with CHCI3- MeOH (10:1) to give 4-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pent-1-ynyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-pheny lcarbamoyl]-butyric acid (21.4 mg, 44%) and 4-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)- S-methyl-phenylJ-propylJ^-methyl-phenylcarbamoyO-butyric acid (6.4 mg, 16%). 4-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pent-1-ynyl]-3-methyl- phenylj-i-ethyl-propyl^-methyl-phenylcarbamoylj-butyric acid ; 1H NMR (CDCI3): 0.12 (3H, s), 0.18 (3H, s), 0.59 (6H, t, J = 7.26 Hz), 0.92 (9H, s), 1.01 (9H, s), 2.00-2.15 (6H, m), 2.19 (3H, s), 2.36 (3H, s), 2.43-2.57 (4H, m), 6.95- 7.05 (5H, m), 7.25 (1 H, d), 7.68 (1 H, d, J = 8.41 Hz) 4-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pent-1-ynyl)-3-me thyl-phenyl]-propyl}- 2-methyl-phenylcarbamoyl)-butyric acid ; 1H NMR (CDCI3): 0.59 (6H, t, J = 7,42 Hz), 1.06 (9H, s), 2.00-2.13 (6H, m), 2.18 (3H, s), 2.37 (3H, s), 2.43-2.57 (4H, m), 6.90-7.04 (5H, m), 7.28 (1 H, d), 7.68 (1 H, d, J = 8.24 Hz) ; MS (ESI+) : 474 ([M+H-H2O]+). Example 266 Preparation of 4-(4-{1 -Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenylcarbamoyl)-butyric acid

HOOC.

Preparation of 4-(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenylcarbamoyl)-butyric acid methyl ester

HOOC MeOOC.

OTBS To a solution of 4-[4-(1-{4-[3-(tert-Butyl-dimethyl-silanyloxy)-4,4-dimethyl- pent-1- ynyl]-3-methyl-phenyl}-1-ethyl-propyl)-2-methyl-phenylcarbam oyl]-butyric acid (compound prepared in Example 265-(9)) (21.4 mg, 0.035 mmol) in MeOH (3 ml) was added Pd(OH)2 (10%, 30 mg) and the mixture was stirred at room temperature under H2 atmosphere overnight. The mixture was filtered through celite and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with CHCI3-MeOH (10:1) to give the title compound (13.5 mg, 76%). 1H NMR (CDCI3): 0.60 (6H, t, J = 7.26 Hz), 0.89 (9H, s), 1.45-1.55 (1 H, m), 1.72- 1.88 (1 H, m), 2.00-2.10 (6H, m), 2.20 (3H, s), 2.25 (3H, s), 2.41-2.50 (4H, m), 2.52-2.62 (1H, m), 2.80-2.92 (1H, m), 3.20-3.30 (1H, m), 3.69 (3H, s), 6.88-7.05 (5H, m), 7.69 (1 H, d, J = 8.74 Hz); MS (ESI+) : 510 [(M+H)+J.

(2) Preparation of 4-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenylcarbamoyl)-butyric acid

MeOOC *■ HOOC To a solution of 4-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2-methyl-phenylcarbamoyl)-butyric acid methyl ester (compound prepared in Example 266-(1)) (11.4 mg, 0.022 mmol) in MeOH (1 ml) was added 1N-NaOH (0.22 ml, 0.220 mmol) and the mixture was stirred at room temperature overnight. The mixture was poured into 1 N-HCI and the products were extacted with CH2CI2. The extracts were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The obtained residue was chromatographed on silica gel with CHCI3-MeOH (10:1) to give the title compound (7.3 mg, 67%). 1H NMR (CDCI3): 0.60 (6H, t, J = 7.25 Hz), 0.89 (9H, s), 1.40-1.62 (1H, m), 1.70- 1.90 (1H, m), 2.00-2.13 (6H, m), 2.19 (3H, s), 2.25 (3H, s), 2.44-2.62 (5H, m), 2.79-2.95 (1 H, m), 3.22-3.27 (1H, m), 6.86-7.05 (5H, m), 7.65 (1H, d, J = 8.24 Hz); MS (ESI+) : 496 [(M+H)+].

Example 267 Preparation of (R)-5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1-methyl-cyclopropyl)-prop-1 - ynyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-p entanoic acid

OH

(1) Preparation of 3-(4-{1-[4-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenyl)-1-(1-methyl-cyclopropyl)-prop -2-yn-1-ol

TBSO TBSO

To a solution of compound prepared in Example 260-(2) (tert-Butyl-{4-[1 -ethyl-1 - (4-ethynyl-3-methyl-phenyl)-propyl]-2-methyl-phenoxy}-dimeth yl-silane) (188 mg, 0.46 mmol) in THF (3 ml), 1.58M n-BuLi in hexane (0.35 ml, 0.55 mmol) was added at -78 degrees C and the mixture was stirred at -78 degrees C for 10min. To the mixture, 1-Methyl-cyclopropanecarbaldehyde (J.Org.Chem. 64, 26, 1999, 9587 - 9595) (0.2 ml) was added at -78 degrees C and the mixture was stirred at room temperature for 16h. To the mixture, hfeO and ethyl acetate were added and the mixture was washed with H2O, dried over MgSO4, concentrated in vacuo and the obtained residue was chromatographed ethyl acetate/n-hexane =0/100 to 3/7) to give the title compound (126 mg, 56%). 1H-NMR: 0.19 (s, 6H), 0.40 (q, 2H), 0.58 (t, 6H)1 0.67-0.72 (m, 2H), 1.00 (s, 9H), 1.27 (s, 3H), 2.01 (q, 4H), 2.14 (s, 3H), 2.37 (s, 3H), 4.26 (d, 1H), 6.61 (d, 1H), 6.77-7.00 (m, 4H), 7.26 (s, 1H)

(2) Preparation of 4-(1 -Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)-prop-1 - ynyl]-3-methyl-phenyl}-propyl)-2-methyl-phenol (Enantiomer A, Enantiomer B)

TBSO

HO I I Enantiomer B OH To a solution of tert-butyl-{4-[1 -ethyl-1 -(4-ethynyl-3-methyl-phenyl)-propyl]-2- methyl-phenoxyj-dimethyl-silane (90 mg, 0.184 mmol) in THF (2 ml), 1M TBAF in THF (0.1 ml) was added at room temperature, and the mixture was stirred at room temperature for 1h and concentrated in vacuo. The obtained residue was chromatographed (ethyl acetate/n-hexane = 0/100 to 1/1) to give the mixture of title compounds (47 mg). The racemic mixture was separated with chiral HPLC (CHIRALPAK OJ-H [DAICEL, 20mml.D., 250mm], ethanol/n-hexane = 10/90) to obtain each enantiomer (Enantiomer A : 20 mg, 100% ee, / Enantiomer B : 15 mg, 100%ee). Enantiomer A: Retention time: 11.874min., Enantiomer B: Retention time: 13.291min. Column: CHIRALPAK OJ-H 4.6x150mm (DAICEL) Eluent: A: n-hexnane, B: EtOH, %B 1 (0min) - 70 (15min) Flow rate: 0.5ml/min. 1H-NMR for mixture EnantiomerA and Enantiomer B: 0.41 (q, 2H), 0.59 (t, 6H), 0.67-0.72 (m, 2H), 1.27 (s, 3H), 2.02 (q, 4H), 2.18 (s, 3H), 2.37 (s, 3H), 4.26 (d, 1 H), 4.67 (s, 1 H), 6.64 (d, 1 H), 6.80-7.00 (m, 4H), 7.26 (d, 1 H) ; MS for mixture Enantiomer A and Enantiomer B (negative mode): 375([M-H]")

(3) Preparation of (R)-5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)- prop-1-ynyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl ]-dihydro-furan-2- one

Enantiomer A OH To a solution of 4-(1-ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)-prop-1-y nyl]- 3-methyl-phenyl}-propyl)-2-methyl-phenol (Enantiomer A) (10 mg, 0.0266 mmol) in DMF (0.5 ml), K2CO3 (10 mg, 0.0725 mmol) and toluene-4-sulfonic acid (R)-5- oxo-tetrahydro-furan-2-ylmethyl ester (10 mg, 0.0756 mmol) were added at room temperature and the mixture was stirred at 90 degrees C for 64 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, concentrated in vacuo and the obtained residue was purified by preparative TLC (n-hexane:ethyl acetate=1:1 and CH2CI2:MeOH=20:1) to give the title compound (6.7 mg, 53%). 1H-NMR: 0.41 (q, 2H), 0.59 (t, 6H), 0.61-0.69 (m ,2H), 1.25 (s, 3H), 1.83 (d, 1 H), 2.02 (q, 4H), 2.14 (s, 3H), 2.37 (s, 3H), 2.38-2.83 (m ,4H), 4.04-4.28 (m, 3H), 4.84-4.92 (m, 1 H), 6.66 (d, 1 h), 6.82-6.98 (m, 4H), 7.25 (d, 1 H); MS (ESI+) : 457 ([M-OH]+). (4) Preparation of (R)-5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)- prop-1-ynyl]-3-methyl-phenyl}-propyl)-2-methylφhenoxy]-4-hy droxy-pentanoic acid

of OH OH To a solution of (R)-5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)-p rop- 1-ynyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dih ydro-furan-2-one (prepared in Example 267-(3)) (6.7 mg, 0.014 mmol) in MeOH (0.5 ml) and THF (0.5 ml), 1NNaOH (0.1 ml) was added at room temperature and the mixture was stirred at room temperature for 1h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (3.3 mg, 47%). 1H-NMR: 0.41 (q, 4H)1 0.60 (t, 6H), 0.64-0.69 (m, 2H), 1.26 (s, 3H), 1.90-2.05 (m, 7H), 2.16 (S, 3H), 2.37 (s, 3H), 2.62 (t, 2H), 3.83-4.10 (m, 3H), 4.25 (s, 1 H), 6.66 (s, 1H), 6.83-7.02 (m, 3H), 7.29 (s, 1H); MS (ESI-) : 491 ([M-HV).

Example 268 Preparation of (R)-5-[4-(1 -Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)-prop-1- ynyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-p entanoic acid

Preparation of (R)-5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)-p rop-1 ■ ynyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dihyd ro-furan-2-one Enantiomer B OH w 0H To a solution of compound prepared in Example 267-(2) (4-(1 -ethyl- 1-{4-[3- hydroxy-3-(1-methyl-cyclopropyl)-prop-1-ynyl]-3-methyl-pheny l}-propyl)-2- methyl-phenol (Enantiomer B) ) (8 mg, 0.0213 mmol) in DMF (0.5 ml), K2CO3 (10 mg, 0.0725 mmol) and toluene-4-sulfonic acid (R)-5-oxo-tetrahydro-furan-2- ylmethyl ester (10 mg, 0.0756 mmol) were added at room temperature and the mixture was stirred at 90 degrees C for 64 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, concentrated in vacuo and the obtained residue was purified by preparative TLC (n-hexane:ethyl acetate=1 :1 and CH2CI2:MeOH=20:1) to give the title compound (4.9 mg, 49%). 1H-NMR: 0.41 (q, 2H), 0.59 (t, 6H), 0.61-0.69 (m ,2H), 1.26 (s, 3H), 1.82 (d, 1 H), 2.02 (q, 4H), 2.14 (s, 3H), 2.37 (s, 3H), 2.38-2.83 (m ,4H), 4.04-4.30 (m, 3H), 4.84-4.92 (m, 1 H), 6.65 (d, 1h), 6.84-6.72 (m, 4H), 7.25 (d, 1H); MS (ESI+) : 457 ([M-OH]+).

(2) Preparation of (R)-5-[4-(1-Ethyl-1-{4-[3-hydroxy-3~(1-methyl-cyclopropyl)- prop-1-ynyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hy droxy-pentanoic acid

OH O' OH OH To a solution of (R)-5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1 -methyl-cyclopropyl)-prop- 1-ynyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dih ydro-furan-2-one (prepared in Example 268-(1)) (4.9 mg, 0.010 mmol) in MeOH (0.5 ml) and THF (0.5 ml), 1 NNaOH (0.1 ml) was added at room temperature and the mixture was stirred at room temperature for 1 h. The mixture concentrated in vacuo, and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (1.3 mg, 25%). 1H-NMR: 0.41 (q, 4H), 0.59 (t, 6H), 0.64-0.69 (m, 2H), 1.27 (s, 3H), 1.90-2.05 (m, 7H), 2.16 (s, 3H), 2.37 (s, 3H), 2.62 (t, 2H), 3.81-4.10 (m, 3H), 4.26 (s, 1 H), 6.66 (S, 1 H), 6.85-7.00 (m, 3H), 7.27 (s, 1 H); MS (ESI-) : 491 ([M-H]").

Example 269 Preparation of (R)- 5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)- propyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy -pentanoic acid

OH i ' OH (1 ) Preparation of 4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1 -methyl-cyclopropyl)-propyl]-3- methyl-phenyl}-propyl)-2-methyl-phenol

OH Enantiomer A Enantiomer 1 To a solution of compound prepared in Example 267-(2) (4-(1-ethyl-1-{4-[3- hydroxy-3-(1-methyl-cyclopropyl)-prop-1-ynyl]-3-methyl-pheny l}-propyl)-2- methyl-phenol (Enantiomer A) ) (15 mg, 0.0399 mmol) in ethyl acetate (2 ml), palladium carbon (5 mg) was added at room temperature and the mixture was stirred at room temperature for 3h under hydrogen gas. The mixture was filtrated through silica and concentrated in vacuo to give the title compound (15 mg, 100%). 1H-NMR: 0.30-0.40 (m, 4H), 0.59 (t, 3H), 1.05 (s, 3H), 1.76-1.84 (m, 2H), 2.03 (q, 4H), 2.19 (s, 3H), 2.25 (s, 3H), 2.53-2.80 (m, 2H), 2.89 (t, 1 H), 4.68 (s, 1 H), 6.64 (d, 1 H), 6.82-7.04 (m, 5H); MS (ESI-) : 379 ([M-H]"). (2) Preparation of (R)- 5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)- propyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dih ydro-furan-2-one

OH

Enantiomer 1 To a solution of 4-(1 -Ethyl-1-{4-[3-hydroxy-3-(1 -methyl-cyclopropyl)-propyl]-3- methyl-phenyl}-propyl)-2-methyl-phenol (Enantiomer 1 prepared in Example 269- (1)) (15 mg, 0.0395 mmol) in DMF (0.5 ml), K2CO3 (10 mg, 0.0725 mmol) and toluene-4-sulfonic acid (R)-5-oxo-tetrahydro-furan-2-ylmethyl ester (10 mg, 0.0756 mmol) were added at room temperature and the mixture was stirred at 90 degrees C for 64 h. To the mixture, ethyl acetate was added and the mixture was washed with H2O, dried over MgSO4, concentrated in vacuo and the obtained residue was purified by preparative TLC (n-hexane:ethyl acetate=1:1 and CH2CI2:MeOH=20:1) to give the title compound (5.2 mg, 28%). 1H-NMR: 0.28-0.42 (m, 4H), 0.59 (t, 6H), 1.05 (s, 3H), 1.26 (t, 1 H), 1.78-1.84 (m, 2H), 2.02 (q, 4H), 2.17 (s, 3H), 2.25 (s, 3H), 2.29-2.92 (m, 6H), 4.01-4.20 (m, 2H), 4.82-4.92 (m, 1H)1 6.66 (d, 1H), 6.89-7.04 (m, 5H); MS (ESI+) : 496 ([M+NH4]+).

(3) Preparation of (R)- 5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)- propyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy -pentanoic acid

O' OH ' ' OH To a solution of ((R)- 5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)- propyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dih ydro-furan-2-one) (prepared in Example 269-(2))(5.2 mg, 0.011 mmol) in MeOH (0.5 ml) and THF (0.5 ml), 1NNaOH (0.1 ml) was added at room temperature and the mixture was stirred at room temperature for 1h. The mixture was concentrated in vacuo, and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (3.9 mg, 73%). 1H-NMR: 0.32-0.42 (m, 4H), 0.59 (t, 6H), 1.05 (s, 3H), 1.78-1.85 (m ,2H), 1.90- 2.00 (m, 2H), 2.05 (q, 4H), 2.15 (s, 3H), 2.25 (s, 3H), 2.56-2.91 (m, 5H), 3.82- 4.15 (m, 3H), 6.67 (d, 1H), 6.89-7.01 (m, 5H); MS (ESI-) : 495 ([M-Hf).

Example 270 Preparation of (R)- 5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)- propyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy -pentanoic acid

OH

Preparation of 4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1 -methyl-cyclopropyl)-propyl]-3- methyl-phenyl}-propyl)-2-methyl-phenol

OH Enantiomer B Enantiomer 2 To a solution of compound prepared in Example 267-(2) (4-(1-ethyl-1-{4-[3- hydroxy-3-(1-methyl-cyclopropyl)-prop-1-ynyl]-3-methyl-pheny l}-propyl)-2- methyl-phenol (Enantiomer B) ) (10 mg, 0.0266 mmol) in ethyl acetate (2 ml), palladium carbon (5 mg) was added at room temperature and the mixture was stirred at room temperature for 3h under hydrogen gas. The mixture was filtrated through silica and concentrated in vacuo to give the title compound (10 mg, 100%). 1H-NMR: 0.30-0.40 (m, 4H), 0.59 (t, 3H), 1.05 (s, 3H), 1.76-1.84 (m, 2H), 2.04 (q, 4H), 2.19 (s, 3H), 2.23 (s, 3H), 2.53-2.80 (m, 2H), 2.88 (t, 1 H), 4.80 (s, 1 H), 6.64 (d, 1 H), 6.82-7.03 (m, 5H); MS (ESi-) : 379 ([M-H]"). (2) Preparation of (R)- 5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)- propyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dih ydro-furan-2-one

OH

Enantiomer 2 To a solution of 4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)-propyl]- 3- methyl-phenyl}-propyl)-2-methyl-phenol4-(1-Ethyl-1 -{4-[3-hydroxy-3-(1 -methyl- cyclopropyl)-propyl]-3-methyl-phenyl}-propyl)-2-methyl-pheno l (Enantiomer 2 prepared in Example 270-(1)) (10 mg, 0.0263 mmol) in DMF (0.5 ml), K2CO3 (10 mg, 0.0725 mmol) and toluene-4-sulfonic acid (R)-5-oxo-tetrahydro-furan-2- ylmethyl ester (10 mg, 0.0756 mmol) were added at room temperature and stirred at 90 degrees C for 64 h. To the mixture, ethyl acetate was added and the organic layer was washed with H2O, dried over MgSO4, concentrated in vacuo and the obtained residue was purified by preparative TLC (n-hexane:ethyl acetate=1 :1 and CH2CI2:MeOH=20:1) to give the title compound (6.7 mg, 53%). 1H-NMR: 0.28-0.42 (m, 4H), 0.59 (t, 6H), 1.05 (s, 3H), 1.26 (t, 1 H), 1.78-1.84 (m, 2H), 2.04 (q, 4H), 2.15 (s, 3H), 2.25 (s, 3H), 2.25-2.95 (m, 6H), 4.01-4.22 (m, 2H), 4.83-4.94 (m, 1H), 6.66 (d, 1H), 6.89-7.04 (m, 5H); MS (ESI+) : 496 ([M+NH4]+).

(3) Preparation of (R)- 5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)- propyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy -pentanoic acid

HOOCs^ OH O' OH ' ' OH To a solution of (R)- 5-[4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopropyl)- propyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dih ydro-furan-2-one (prepared in Example 270-(2))(6.7 mg, 0.014 mmol) in MeOH (0.5 ml) and THF (0.5 ml), 1 NNaOH (0.1 ml) was added at room temperature and the mixture was stirred at room temperature for 1h. The mixture was concentrated in vacuo, and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (3.6 mg, 52%). 1H-NMR: 0.32-0.41 (m, 4H), 0.59 (t, 6H), 1.05 (s, 3H), 1.26 (s, 1 H), 1.77-1.85 (m ,2H), 1.89-2.00 (m, 2H), 2.02 (q, 4H), 2.17 (s, 3H), 2.25 (s, 3H), 2.58-2.92 (m, 5H), 3.82-4.15 (m, 3H), 6.67 (d, 1H), 6.89-7.01 (m, 5H); MS (ESI-) : 495 ([M-H]').

Example 271 Preparation of (R)-5-[4-(1 -Ethyl-1 -{4-[3-(1 -ethyl-cyclopropyl)-3-hydroxy-propyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy-pentanoic acid

HO2* OH ' ' OH (1 ) Preparation of Cyclopropanecarboxylic acid 2, 6-di-tert-butyl-4-methyl-phenyl ester -V

W //

n-BuLi (2.44 mol/l in hexane) (22.7- mmol) was added to an ice-cooled solution of 2, 6-Di-t-butyl-p-cresol (5.0 g, 22.7 mmol) in 25 ml of THF. After a period of 15 min, Cyclopropanecarbonyl Chloride (2.5 g, 23.8 mmol) was added and the mixture stirred at room temperature for 24h and poured onto 10 ml of saturated aqueous NH4CI. After separation of the layers, the aqueous layer was extracted with 25 ml of ether, and the organic phase were combined and washed with saturated aqueous NaHCO3 and brine, dried over MgSO4, and concentrated in vacuo. The residue was chromatographed on silica gel (ethyl acetate/hexane = 0/100 to 10/90) to give the title compound (5.6 g, 85%). 1H-NMR: 1.00-1.07 (m, 2H), 1.13-1.18 (m, 2H), 1.34 (s, 18H), 1.89-1.97 (m, 1H), 2.31 (s, 3H), 7.10 (s, 2H); MS (ESI+) : 306 ([M+NH4∏.

(2) Preparation of 1-Ethyl-cyclopropanecarboxylic acid 2,6-di-tert-butyl-4-methyl- phenyl ester

<VO-

" To a solution of Cyclopropanecarboxylic acid 2, 6-di-tert-butyl-4-methyl-phenyl ester (compound prepared in Example 271 -(1)) (3.0 g, 10.4 mmol) in THF (20 ml) was added t-BuLi (1.47 mol/l in n-pentane) (11.4 mmol) at -78 degrees C. The solution was stirred under N2 for 30 min, and Ethyl Iodide (1.9 g, 12.5 mmol, dissolved in 3 ml of THF) was added. The solution was allowed to warm to room temperature within 4h. The reaction was quenched with saturated aqueous NH4CI. The mixture was diluted with Et2O, washed with saturated aqueous NH4CI and brine, dried over MgSO4, and concentrated in vacuo to give the title compound (320 mg, 37%). 1H-NMR: 0.89-0.93 (m, 2H), 1.05 (t, J=7.3 Hz, 3H), 1.32 (s, 18H), 1.45-1.52 (m, 2H), 1.82 (q, J=7.3 Hz, 2H), 2.30 (s, 3H), 7.09 (s, 2H)

(3) Preparation of 1-Ethyl-cyclopropanecarboxylic acid

^r Y 1J w 1 S±-TΓ ^k A suspension of 1-Ethyl-cyclopropanecarboxylic acid 2,6-di-tert-butyl-4-methyl- phenyl ester (compound prepared in Example 271 -(2)) (2.41 g, 7.6 mmol), t- BuOK (5.13 g, 45.7 mmol), and H2O (274 mg, 15.2 mmol) in 38 ml of THF was heated under reflux for 36h. After extraction with 2N KOH, the H2O phase was acidified with concentrated HCI, extracted with Et2O. The extracts were dried over MgSO4 and concentrated in vacuo and the obtained residue was chromatographed on silica gel (Et2O/n-pentane = 3/97) to give the title compound (2.41 g, 73%). 1H-NMR: 0.73-0.81 (m, 2H), 1.01 (t, J=7.3 Hz, 3H), 1.22-1.30 (m, 2H), 1.56 (q, J=7.3 Hz, 2H); MS (ESI+) : 251 ([2xM+Na]+).

(4) Preparation of 1-Ethyl-cyclopropanecarboxylic acid N-methoxy-N-methyl- amide

°γ0H ^ oΛ /"Δ Ok To a solution of 1-Ethyl-cyclopropanecarboxylic acid (compound prepared in Example 271 -(3)) (320 mg, 2.8 mmol) in dichloromethane (10 ml) was added methoxymethylamine hydrochloride (328 mg, 3.4 mmol), 4- dimethylaminopyridine (171 mg, 1.4 mmol), triethyamine (793 mg, 7.8 mmol), and 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (751 mg, 3.9 mmol) at 0 degrees C. The solution was stirred under N2 for 2Oh, and diluted with ethyl acetate, washed with 1 N HCI, saturated aqueous NaHCO3 and brine, dried over MgSO4, and concentrated in vacuo. The residue was chromatographed on silica gel (ethyl acetate/hexane = 0/100 to 40/60) to give the title compound (200 mg, 45%). 1H-NMR: 0.55-0.57 (m, 2H), 0.93-1.02 (m, 5H), 1.59 (q, J=7.7 Hz, 2H), 3.25 (s, 3H), 3.72 (s, 3H); MS (ESI+) : 158([M+H]+).

(5) Preparation of 3-(4-{1-[4-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenyl)-1-(1-ethyl-cyclopropyl)-prop- 2-yn-1-one To a solution of tert-Butyl-{4-[1-ethyM-(4-ethynyl-3-methyl-phenyl)-propyl]-2 - methyl-phenoxyj-dimethyl-silane (compound prepared in Example 260-(1)) (345 mg, 0.85 mmol) in THF (2 ml) was added n-BuLi (2.44 mol/l in hexane) (1.19 mmol) at -78 degrees C. The solution was stirred at room temperature under N2 for 20 min. The solution was cooled to -78 degrees C, and added THF solution (0.5 ml) of 1-Ethyl-cyclopropanecarboxylic acid N-methoxy-N-methyl-amide (compound prepared in Example 271-(4)) (200 mg, 1.27 mmol). The solution was allowed to warm to room temperature overnight. The reaction was quenched with saturated aqueous NH4CI, extracted with ethyl acetate, washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was chromatographed on silica gel (ethyl acetate/hexane = 0/100 to 5/95) to give the title compound (380 mg, 89%). 1H-NMR: 0.20 (s, 6H), 0.59 (t, J=7.0 Hz, 6H), 0.95-1.06 (m, 14H), 1.51-1.56 (m, 2H), 1.73 (q, J= 7.3 Hz, 2H), 2.03 (q, J=7.0 Hz, 4H), 2.14 (s, 3H), 2.41 (s, 3H), 6.63 (d, J=8.4 Hz, 1 H), 6.79 (d, J=8.1 Hz, 1 H), 6.84 (s, 1H), 6.99 (d, J=8.1 Hz, 1 H), 7.04 (s, 1 H), 7.38 (d, J=8.1 Hz, 1 H); MS (ESI+) : 503([M+H]+).

(6) Preparation of 3-(4-{1-[4-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenyl)-1-(1-ethyl-cyclopropyl)-prop- 2-yn-1 -ol

O OH To a solution of 3-(4-{1-[4-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenyl)-1 -(1 -ethyl-cyclopropyl)-prop-2-yn-1 -one (compound prepared in Example 271 -(5)) (380 mg, 0.76 mmol) in THF/MeOH (4 ml/4 ml) was added NaBH4 (86 mg, 2.28 mmol) at room temperature. The solution was stirred at room temperature under N2 for 1 h, quenched with H2O, and extracted with ethyl acetate, washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was chrornatographed on silica gel (ethyl acetate/hexane = 0/100 to 10/90) to give the title compound (350 mg, 91%). 1H-NMR: 0.19 (s, 6H), 0.35-0.46 (m, 2H), 0.58 (t, J=I.3 Hz, 6H), 0.68-0.78 (m, 2H), 0.95-1.03 (m, 12H), 1.30-1.40 (m, 1H), 1.74 (d, J=7.0 Hz, 1 H), 1.87-1.96 (m, 1H), 2.03 (q, J=7.0 Hz, 4H), 2.14 (s, 3H), 2.36 (s, 3H), 4.63 (d, J=7.0 Hz, 1 H), 6.62 (d, J=8.4 Hz, 1 H), 6.79 (d, J=8.8 Hz, 1 H), 6.85 (s, 1 H), 6.92 (d, J=8.1 Hz, 1 H), 6.99 (s, 1H)1 7.25 (m, 1 H); MS (ESI-) : 503([M-H]").

(7) Preparation of 4-(1-Ethyl-1-{4-[3-(1-ethyl-cyclopropyl)-3-hydroxy-prop-1-yn yl]- 3-methyl-phenyl}-propyl)-2-methyl-phenol

H To a solution of 3-(4-{1 -[4-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-phenyl]-1 - ethyl-propyl}-2-methyl-phenyl)-1 -(1-ethyl-cyclopropyl)-prop-2-yn-1 -ol (compound prepared in Example 271 -(6)) (350 mg, 0.69 mmol) in THF (7 ml) was added tetrabutylammonium fluoride (1 M in THF) (1.0 mmol) at room temperature. The solution was stirred at room temperature under N2 for 30 min, and diluted with ethyl acetate, washed with diluted KHSO4 and brine, dried over MgSO4, and concentrated in vacuo. The residue was chromatographed on silica gel (ethyl acetate/hexane = 0/100 to 40/60) to give the title compound (240 mg, 89%). 1H-NMR: 0.35-0.46 (m, 2H), 0.59 (t, J=7.3 Hz, 6H), 0.68-0.78 (m, 2H), 0.97 (t, J=7.7 Hz, 3H), 1.29-1.41 (m, 1 H), 1.74 (d, J=7.0 Hz, 1 H), 1.87-1.97 (m, 1H), 2.02 (q, J=7.3 Hz, 4H), 2.19 (s, 3H), 2.36 (s, 3H), 4.57 (d, J=4.4 Hz, 1 H), 4.63 (d, J=6.6 Hz, 1 H), 6.65 (d, J=8.1 Hz, 1H), 6.83-6.88 (m, 2H), 6.92 (d, J=8.1 Hz, 1H), 6.99 (s, 1H), 7.28-7.30 (m, 1H); MS (ESI-) : 389([M-H]-).

(8) Preparation of 4-(1-Ethyl-1-{4-[3-hydroxy-3-(1-ethyl-cyclopropyl)-propyl]-3 - methyl-phenyl}-propyl)-2-methyl-phenol A solution of 4-(1 -Ethyl-1 -{4-[3-(1 -ethyl-cyclopropyO-S-hydroxy-prop-i -ynyl]-3- methyl-phenyl}-propyl)-2-methyl-phenol (compound prepared in Example 271- (7)) (38 mg, 0.097 mmol) in AcOEt/MeOH (1 ml/1 ml) was hydrogenated on 10% palladium on carbon (5 mg) as catalyst. After4h the reaction mixture was filtered through a Celite, the filtrate was concentrated in vacuo. The residue was purified by preparative TLC (ethyl acetate/hexane = 1/3) to give the title compound (33 mg, 87%). 1H-NMR: 0.30-0.42 (m, 4H), 0.59 (t, J=7.3 Hz, 6H), 0.87 (t, J=7.3 Hz, 3H), 1.20- 1.38 (m, 2H), 1.60-1.72 (m, 1 H), 1.73-1.86 (m, 2H), 2.02 (q, J=7.7 Hz1 4H), 2.20 (s, 3H), 2.25 (s, 3H), 2.53-2.62 (m, 1H), 2.72-2.82 (m, 1 H), 3.08-3.15 (m, 1 H), 4.55 (s, 1 H), 6.64 (d, J=8.1 Hz, 1 H), 6.85-6.95 (m, 4H), 7.01 (d, J=8A Hz, 1H); MS (ESI-) : 393([M-H]-).

(9) Preparation of (R)-5-[4-(1 -Ethyl-1 -{4-[3-(1-ethyl-cyclopropyl)-3-hydroxy- propyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dih ydro-furan-2-one

H V° OH

To a solution of 4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1-ethyl-cyclopropyl)-propyl]-3- methyl-phenyl}-propyl)-2-methyl-phenol (compound prepared in Example 271- (8)) (33 mg, 0.084 mmol) in dimethylacetamide (0.8 ml), K2CO3 (35 mg, 0.252 mmol) was added and stirred at room temperature. To the mixture, (R)-(-)- dihydro-5-(p-tolylsulfonyloxymethyl)-2-(3H)-furanone (34 mg, 0.126 mmol) was added and stirred at 100 degrees C for 15 h. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate, washed with H2O and brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by preparative TLC (ethyl acetate/hexane = 2/3) to give the title compound (24 mg, 58%). 1H-NMR: 0.31-0.42 (m, 4H), 0.59 (t, J=7.3 Hz, 6H), 0.86 (t, J=7.3 Hz, 3H), 1.20- 1.40 (m, 2H), 1.60-1.72 (m, 1H), 1.73-1.82 (m, 2H), 2.03 (q, J=7.3 Hz, 4H), 2.15 (s, 3H), 2.25 (s, 3H), 2.28-2.50 (m, 2H)1 2.52-2.62 (m, 2H), 2.72-2.82 (m, 2H), 3.08-3.15 (m, 1 H), 4.02-4.20 (m, 2H), 4.85-4.92 (m, 1 H), 6.65 (d, J=8.4 Hz, 1 H), 6.85-6.97 (m, 4H), 7.01 (d, J=8.4 Hz, 1 H); MS (ESI-) : 491([M-H]").

(10) Preparation of (R)-5-[4-(1-Ethyl-1-{4-[3-(1-ethyl-cyclopropyl)-3-hydroxy- propyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4-hydroxy -pentanoic acid

H OH

To a solution of (R)-5-[4-(1-Ethyl-1-{4-[3-(1-ethyl-cyclopropyl)-3-hydroxy-pr opyl]- 3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dihydro-fur an-2-one (compound prepared in Example 271 -(9)) (21 mg, 0.084 mmol) in THF/MeOH (2.5 ml/2.5 ml ), 1 N NaOH (0.5 ml) was added at room temperature and stirred at room temperature for 1h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3:MeOH=8:3 saturated with H2O) to give the title compound (21 mg, 96%). 1H-NMR: 0.30-0.42 (m, 4H), 0.59 (t, J=7.0 Hz, 6H), 0.86 (t, J=7.3 Hz, 3H), 1.23- 1.37 (m, 1 H), 1.60-1.72 (m, 1H), 1.73-2.20 (m, 9H), 2.16 (s, 3H), 2.25 (s, 3H), 2.53-2.65 (m, 3H), 2.72-2.80 (m, 1 H)1 3.08-3.15 (m, 1 H), 3.80-3.98 (m, 2H), 4.00-4.09 (m, 1 H), 6.66 (d, J=8A Hz, 1 H), 6.85-6.97 (m, 4H), 7.01 (d, J=8.1 Hz1 1 H); MS (ESI-): 509([M-H]").

Example 272 Preparation of (R)-5-(4-{1 -Ethyl-1 -[3-methyl-4-(5,5,5-trifluoro-3-hydroxy-4- methyl-4-trifluoromethyl-pentyl)-phenyl]-propyl}-2-methyl-ph enoxy)-4-hydroxy- pentanoic acid

HO2C (1) Preparation of 1-(441-[4-(tert-Butyl-dimethyl-s∏anyloxy)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenyl)-5,5,5-trifluoro-4-methyl-4-tr ifluoromethyl-pent-1- yn-3-one

CF3 TBSO TBSO

To a solution of tert-Butyl-{4-[1-ethyl-1-(4-ethynyl-3-methyl-phenyl)-propyl] -2- methyl-phenoxyj-dimethyl-silane (compound prepared in Example 260-(1)) (296.3 mg, 0.729 mmol) in THF (1.2 ml), 2.44 M n-butyl lithium in hexane (0.420 ml, 1.02 mmol) was added at -78 degrees C. To the mixture, 3,3,3-Trifluoro-2- methyl-2-trifluoromethyl-propionyl fluoride (0.160 ml, 1.11 mmol) in THF (0.5 ml) was added at -78 degrees C, the mixture was stirred at -78 degrees C to room temperature overnight. To the mixture, brine was added. The products were extracted with ethyl acetate and the extracts were dried over MgSO4, concentrated in vacuo. The obtained residue was chromatographed on silica gel (ethyl acetate/hexane = 0/100 to 3/97) to give the title compound (289.8 mg, 66 %). 1H-NMR (chloroform-d): 0.20 (s, 6H), 0.59 (t, 6H, J=7.1 Hz), 1.00 (s, 9H), 1.77 (s, 3H), 2.04 (q, 4H, J=7.2Hz), 2.14 (s, 3H), 2.45 (s, 3H), 6.64 (d, 1 H, J=8.4Hz), 6.79 (d, 1 H, J=8.8Hz), 6.84 (s, 1 H), 7.04 (d, 1H, J=7.7Hz), 7.09 (s, 1 H), 7.47 (d, 1 H, J=8.4Hz); MS (ESI+): 599 ([MH-H]+).

(2) Preparation of 1-(4-{1-[4-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenyl)-5,5,5-trifluoro-4-methyl-4-tr ifluoromethyl-pent-1- yn-3-ol

TBSO TBSO' To a solution of 1-(4-{1-[4-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenyl)-5,5,5-trifluoro-4-methyl-4-tr ifluoromethyl-pent-1- yn-3-one (compound prepared in Example 272-(1)) (289 mg, 0.483 mmol) in MeOH (1 ml) and THF (4 ml), NaBH4 was added at room temperature, and the mixture was stirred at room temperature for 30 min. To the mixture, ethyl acetate was added and the solution was washed with brine, dried over MgSO4, concentrated in vacuo. The obtained residue was chromatographed on silica gel (ethyl acetate/hexane = 0/100 to 5/95) to give the title compound (209.9 mg, 72 %). 1H-NMR (chloroform-d): 0.19 (s, 6H), 0.58 (t, 6H, J=7.1 Hz), 1.00 (s, 9H), 1.54 (s, 3H), 2.02 (q, 4H, J=7.1Hz), 2.14 (s, 3H), 2.28 (d, 1H, J=8.1Hz), 2.36 (s, 3H), 0.00 (d, 1 H1 J=7.7Hz), 6.63 (d, 1 H, J=8.4Hz), 6.80 (d, 1 H, J=8.4Hz), 6.85 (s, 1 H), 6.96 (d, 1 H, J=8.0Hz), 7.02 (s, 1 H), 7.28 (d, 1 H, J=8.4Hz); MS(ESI+): 601 ([M+H]+).

(3) Preparation of Acetic acid 3-(4-{1-[4-(tert-butyl-dimethyl-silanyloxy)-3-methyl- phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-1 -(2,2,2-trifluoro-1-methyl- 1 - trifluoromethyl-ethyl)-prop-2-ynyl ester

TBSO' TBSO

OAc To a solution of 1-(4-{1-[4-(tert-Butyl-dimethyl-silanyloxy)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenyl)-5,5,5-trifluoro-4-methyl-4-tr ifluoromethyl-pent-1- yn-3-ol (compound prepared in Example 272-(2)) (23.8 mg, 0.0396 mmol) in CH2CI2 (1 ml), pyridine (0.0096 ml) and Ac2O (0.0056 ml) were added at room temperature, and the mixture was stirred at room temperature for 12 h. CH2CI2 was removed in vacuo and pyridine (0.3 ml) and Ac2O (0.0112 ml) were added to the mixture again and the mixture was stirred at room temperature for 1.5 h. To the mixture ethyl acetate was added and the solution was washed with dil.HCI and brine, dried over MgSO4, concentrated in vacuo. The obtained residue was purified by preparative TLC (ethyl acetate/hexane = 1/20) to give the title compound (21.3 mg, 84 %). 1H-NMR (chloroform-d): 0.19 (s, 6H), 0.58 (t, 6H, J=7.1 Hz), 1.00 (s, 9H), 1.59 (s, 3H), 2.02 (q, 4H, J=7.2Hz), 2.14 (s, 3H), 2.14 (s, 3H), 2.34 (s, 3H), 6.11 (s, 1 H), 6.62 (d, 1 H, J=8.8Hz), 6.78 (d, 1 H, .7=8.1 Hz), 6.84 (s, 1 H), 6.94 (d, 1 H, J=8.8Hz), 7.00 (s, 1 H), 7.28 (d, 1H, J=8.1 Hz); MS(ESI+): 665 ([Mn-Na]+).

(4) Preparation of Acetic acid 3-{4-[1-ethyl-1-(4-hydroxy-3-methyl-phenyl)- propyl]-2-methyl-phenyl}-1 -(2,2,2-trifluoro-1 -methyl-1 -trifluoromethyl-ethyl)-prop- 2-ynyl ester

CF3 TBSO 'CF3 OAc OAc To a solution of Acetic acid 3-(4-{1-[4-(tert-butyl-dimethyl-silanyloxy)-3-methyl- phenyl]-1 -ethyl-propyl}-2-methyl-phenyl)-1 -(2,2,2-trifluoro-1 -methyl-1 - trifluoromethyl-ethyl)-prop-2-ynyl ester (compound prepared in Example 272-(3)) (19.9 mg, 0.0310 mmol) in THF (2 ml), 1 M terabutylammonium fluoride in THF (0.040 ml, 0.040 mmol) was added. The mixture was stirred for 5 min. To the mixture, ethyl acetate was added and the solution was washed with brine, dried over MgSO4, concentrated in vacuo, The obtained residue was purified by preparative TLC (ethyl acetate/hexane = 1/10) to give the title compound (14.1 mg, 86 %). 1H-NMR (chloroform-d): 0.58 (t, 6H, J=7.3Hz), 1.59 (s, 3H), 2.02 (q, 4H, J=7.0Hz), 2.14 (s, 3H), 2.18 (s, 3H), 2.34 (s, 3H), 4.85 (brs, 1H), 6.11 (s, 1H), 6.65 (d, 1 H, J=8.0Hz), 6.82 (d, 1 H, J=8.1 Hz), 6.83 (s, 1 H), 6.95 (d, 1 H, J=8.4Hz), 7.00 (s, 1 H, J=8.4Hz); MS(ESI-): 527 ([M-H]").

(5) Preparation of Acetic acid 1-(2-{4-[1-ethyl-1-(4-hydroxy-3-methyl-phenyl)- propyl]-2-methyl-phenyl}-ethyl)-2,2-dimethyl-propyl ester OAc OAc To a solution of Acetic acid 3-{4-[1-ethyl-1-(4-hydroxy-3-methyl-phenyl)-propyl]- 2-methyl-phenyl}-1 -(2,2,2-trifluoro-i -methyl-1 -trifluoromethyl-ethyl)-prop-2-ynyl ester (compound prepared in Example 272-(4)) (14.1mg, 0.0267 mmol) in MeOH (2 ml), 10%Pd/C (4.7 mg) was added. The mixture was stirred at room temperature for 13 h under hydrogen. The mixture was filtered, concentrated in vacuo and purified by preparative TLC (ethyl acetate/hexane = 1/5) to give the title compound (12.9 mg, 91 %). 1H-NMR (chloroform-d): 0.59 (t, 6H1 J=7.3Hz), 1.37 (s, 3H), 1.90-2.05 (m, 6H), 2.12 (s, 3H), 2.19 (s, 3H), 2.20 (s, 3H), 2.45-2.58 (m, 2H), 4.69 (brs, 1 H), 5.47 (d, 1H), 6.65 (d, 1H), 6.84-6.99 (m, 5H); MS(ESI-): 531 ([M-H]").

(6) Preparation of Acetic acid 1-[2-(4-{1 -ethyl- 1-[3-methyl-4-((R)-5-oxo- tetrahydro-furan-2-ylmethoxy)-phenyl]-propyl}-2-methyl-pheny l)-ethyl]-3,3,3- trifluoro-2-methyl-2-trifluoromethyl-propyl ester

OAc OAc

To a solution of Acetic acid 1-(2-{4-[1-ethyl-1-(4-hydroxy-3-methyl-phenyl)- propyl]-2-methyl-phenyl}-ethyl)-2,2-dimethyl-propyl ester (compound prepared in Example 272-(5)) (12.9 mg, 0.0242 mmol) in N,N-dimethylacetamide (0.5 ml), K2CO3 (11.1 mg, 0.0803 mmol) and (R)-(-)-dihydro-5-(p-tolylsulfonyloxymethyl)- 2(3H)-furanone (10.2 mg, 0.0377 mmol) were added. The mixture was stirred at 90 degrees C for 27 h. After cooled to room temperature, (R)-(-)-dihydro-5-(p- tolylsulfonyloxymethyl)-2(3H)-furanone (10.2 mg, 0.0377 mmol) was added. The mixture was stirred at 90 degrees C for 14 h. After cooled to room temperature, the mixture was poured into brine and the products were extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, concentrated in vacuo. The obtained residue was purified by preparative TLC (ethyl acetate/hexane = 1/1) to give the title compound (11.2 mg, 73 %). 1H-NMR (chloroform-d): 0.58 (t, 6H, J=IA Hz), 1.37 (s, 3H), 1.92-2.06 (m, 6H), 2.12 (S, 3H), 2.15 (s, 3H), 2.20 (s, 3H), 2.24-2.36 (m, 1H), 2.39-2.61 (m, 4H), 2.73-2.82 (m, 1 H), 4.06 (dd, 1 H, J=3.4, 10.2Hz), 4.16 (dd, 1 H, J=3.2, 10.4Hz), 4.87-4.90 (m, 1 H), 5.46 (d, 1H), 6.66 (d, 1H), 6.90-7.00 (m, 5H); MS(ESI+): 631 ([M+H]+).

(7) Preparation of (R)-5-(4-{1-Ethyl-1-[3-methyl-4-(5,5,5-trifluoro-3-hydroxy-4 - methyl-4-trifluoromethyl-pentyl)-phenyl]-propyl}-2-methyl-ph enoxy)-4-hydroxy- pentanoic acid

OAc SH ' ' OH ϋ To a solution of Acetic acid 1-[2-(4-{1-ethyl-1-[3-methyl-4-((R)-5-oxo-tetrahydro- furan^-ylmethoxyJ-phenylJ-propylJ^-methyl-phenyO-ethy∏-S.S .S-trifluoro^- methyl-2-trifluoromethyl-propyl ester (compound prepared in Example 272-(6)) (6.8 mg, 0.0108 mmol) in MeOH (0.5 ml) and THF (0.5 ml), 1 N NaOH solution was added. The mixture was stirred at room temperature for 5.5 h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3/MeOH = 8/3 saturated with H2O) to give the title compound (4.7 mg, 72 %). 1H-NMR (chloroform-d): 0.59 (t, 6H, J=7.3Hz), 1.35 (s, 3H), 1.74-2.06 (m, 8H), 2.16 (s, 3H), 2.25 (s, 3H), 2.57-2.63 (m, 3H), 2.91-2.98 (m, 1 H), 3.83-3.90 (m, 2H), 3.97 (d, 1 H, J=9.2Hz), 4.04-4.11 (m, 1 H), 6.67 (d, 1 H, J=8.5Hz), 6.91-6.96 (m, 4H), 7.00 (d, 1 H, J=8.0Hz); MS(ESI+): 607([M+H]+).

Example 273 Preparation of 5-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-(E)-but-1-enyl)-phenyl]-propyl}-2-methyl-phe nyl)-pent-4-ynoic acid HOOC (1 ) Preparation of Trifluoro-methanesulfonic acid 4-{1-ethyl-1-[3-methyl-4-(4,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-(E)-but-1-enyl) -phenyl]-propyl}-2- methyl-phenyl ester

TfO OMOM _ ΌMOM UF3 CF3 To a solution of 4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-methoxymethoxy-3 - trifluoromethyl-(E)-but-1-enyl)-phenyl]-propyl}-2-methyl-phe nol (compound prepared in Example 30-(1 )) (0.2 g, 0.4 mmol) in dichloromethane (4 ml), pyridine (0.07 ml, 0.87 mmol), and Tf2O (0.08 ml, 0.48 mmol) were added at 0 degrees C and the mixture was stirred at room temperature for 15 minutes. To the mixture, ethyl acetate was added and the mixture was washed with water, dried over MgSO4, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (ethyl acetate/hexane =1/20) to give the title compound (0.22 g, 87%) as colorless oil. 1H-NMR (CDCI3): 0.61 (t, 6H, J=7.3Hz), 2.08 (q, 4H, J=7.3Hz), 2.32 (s, 3H), 2.33 (s, 3H), 2.50 (s, 3H), 4.97 (s, 2H), 6.08 (d, 1H, J=16.6Hz), 6.95-7.15 (m, 5H), 7.30-7.40 (m, 2H).

(2) Preparation of Trifluoro-methanesulfonic acid 4-{1 -ethyl-1 -[3-methyl-4-(4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-(E)-but-1-enyl)-phenyl ]-propyl}-2-methyl- phenyl ester

TfO TfO ΌMOM CF3 To a solution of Trifluoro-methanesulfonic acid 4-{1-ethyl-1-[3-methyl-4-(4,4,4- trifluoro-3'methoxymethoxy-3-trifluoromethyl-(E)-but-1-enyl) -phenyl]-propyl}-2- methyl-phenyl ester (compound prepared in Example 273-(1) (220 mg, 0.35 mmol) in dichloromethane (0.75 ml), trifluoroacetic acid (0.25 ml) was added at room temperature and the mixture was stirred at room temperature for 14 h. The mixture was concentrated in vacuo, and chromatographed on silica gel (ethyl acetate/hexane =1/10) to give the title compound (180 mg, 88%) as colorless oil. 1H-NMR (CDCI3): 0.61 (t, 6H, J=7.3Hz), 2.08 (q, 4H, J=7.3Hz), 2.32 (s, 3H), 2.35 (s, 3H), 3.43 (s, 1H), 6.09 (d, 1 H, J=15.8Hz), 6.90-7.15 (m, 5H), 7.30-7.45 (m, 2H).

(3) Preparation of 5-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-(E)-but-1-enyl)-phenyl]-propyl}-2-methyl-phe nyl)-pent-4-ynoic acid methyl ester

TfO ' ' CFs " ' MeOOC

To a solution of trifluoro-methanesulfonic acid 4-{1 -ethyl-1 -[3-methyl-4-(4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-(E)-but-1-enyl)-phenyl ]-propyl}-2-methyl- phenyl ester (compound prepared in Example 273-(2)) (30 mg, 0.05 mmol) in DMF (1 ml), PdCI2(dppf)2-CH2Cl2 (4 mg, 0.005 mmol), Et3N (0.024 ml, 0.17 mmol), CuI (10 mg, 0.05 mmol), and pent-4-ynoic acid methyl ester (11 mg, 0.1 mmol) were added at room temperature under nitrogen and stirred at 120 degrees C for 14 h. To the mixture, ethyl acetate was added and the mixture was washed with water and brine, dried over MgSO4, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (ethyl acetate/hexane =1/5) to give the title compound (20 mg, 71%) as colorless oil. 1H-NMR (CDCI3): 0.60 (t, 6H, J=7.3Hz), 2.06 (q, 4H, J=7.3Hz), 2.32 (s, 3H), 2.33 (s, 3H), 2.55-2.80 (m, 4H), 3.12 (s, 1 H), 3.71 (s, 3H), 6.08 (d, 1 H, J=15.8Hz), 6.80-7.00 (m, 4H), 7.23 (d, 1 H, J=8.1Hz), 7.30-7.40 (m, 2H). (4) Preparation of 5-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-CEJ-but-i-enyO-pheny∏-propylJ^-methyl-phen ylJ-pθnt^-ynoic acid

^cF3 ► ,y<^ MeOOC" ^^ ' ' CFa HOOC" To a solution of 5-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-CEJ-but-i-enyO-phenylJ-propylJ^-methyl-pheny lJ-penM-ynoic acid methyl ester (compound prepared in Example 273-(3)) (20 mg, 0.036mmol) in MeOH (1 ml), 1 N NaOH aq. (0.2 ml, 0.2 mmol) was added at room temperature and stirred at room temperature for 4 h. To the mixture, ethyl acetate was added and the mixture was washed with 30% NaHaPO4 aq., dried over MgSO4, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (ethyl acetate/hexane =3/1) to give the title compound (12 mg, 62%) as colorless oil. 1H-NMR (CDCI3): 0.60 (t, 6H, J=7.3Hz), 2.06 (q, 4H, J=7.3Hz), 2.32 (s, 3H), 2.34 (s, 3H), 2.60-2.85 (m, 4H), 6.08 (d, 1 H, J=15.7Hz), 6.80-7.00 (m, 4H), 7.23 (d, 1H, J=7.9Hz), 7.30-7.40 (m, 2H); MS(ESI+): 541([M+H]+)

Example 274 Preparation of 6-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl^EJ-but-i-enyO-pheny^-propylJ^-methyl-phenyO- hex-δ-ynoic acid

HOOC

(1) Preparation of 6-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-(E)-but-1-enyl)-phenyl]-propyl}-2-methyl-phe nyl)-hex-5-ynoic acid methyl ester TfO MeOOC

To a solution of trifluoro-methanesulfonic acid 4-{1 -ethyl- 1-[3-methyl-4-(4 ,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-(E)-but-1-enyl)-phenyl ]-propyl}-2-methyl- phenyl ester (compound prepared in Example 273-(2)) (30 mg, 0.05 mmol) in DMF (1 ml), PdCI2(dppf)2-CH2Cl2 (4 mg, 0.005 mmol), Et3N (0.024 ml, 0.17 mmol), CuI (10 mg, 0.05 mmol), and hex-5-ynoic acid methyl ester (13 mg, 0.1 mmol) were added at room temperature under nitrogen and stirred at 120 degrees C for 14 h. To the mixture, ethyl acetate was added and the mixture was washed with water and brine, dried over MgSO4, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (ethyl acetate/hexane =1/5) to give the title compound (20 mg, 69%) as colorless oil. 1H-NMR (CDCI3): 0.60 (t, 6H, J=7.3Hz), 1.80-2.00 (m, 2H), 2.08 (q, 4H, J=7.2Hz), 2.33 (s, 3H), 2.35 (s, 3H), 2.45-2.60 (m, 4H), 3.68 (s, 3H), 6.08 (d, 1H, J=15.7Hz), 6.84-7.02 (m, 4H), 7.20-7.28 (m, 1 H), 7.30-7.40 (m, 2H).

(2) Preparation of 6-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-(E)-but-1-enyl)-phenyl]-propyl}-2-methyl-phe nyl)-hex-5-ynoic acid

MeOOC HOOC

To a solution of 6-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-(E)-but-1-enyl)-phenyl]-propyl}-2-methyl-phe nyl)-hex-5-ynoic acid methyl ester (compound prepared in Example 274-(1)) (20 mg, 0.035mmol) in MeOH (1 ml), 1 N NaOH aq. (0.2 ml, 0.2 mmol) was added at room temperature and stirred at room temperature for 4 h. To the mixture, ethyl acetate was added and the mixture was washed with 30% NaH2PO4 aq., dried over MgSO4, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (ethyl acetate/hexane =3/1 ) to give the title compound (14 mg, 72%) as colorless oil. 1H-NMR (CDCI3): 0.60 (t, 6H1 J=7.3Hz), 1.85-2.00 (m, 2H), 2.06 (q, 4H, J=7.2Hz), 2.33 (s, 3H), 2.35 (s, 3H), 2.54 (t, 2H, J=6.8Hz), 2.58 (t, 2H, J=7.4Hz), 6.11-6.05 (d, 1 H, J=15.8Hz), 6.85-7.05 (m, 4H), 7.20-7.27 (m, 1 H), 7.30-7.40 (m, 2H); MS(ESI+): 555([M+H]+)

Example 275 Preparation of 7-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-(E)-but-1-enyl)-phenyl]-propyl}-2-methyl-phe nyl)-hept-6-ynoic acid

HOOC (1 ) Preparation of 7-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-(E)-but-1-enyl)-phenyl]-propyl}-2-methyl-phe nyl)-hept-6-ynoic acid methyl ester

TfO MeOOC

To a solution of trifluoro-methanesulfonic acid 4-{1-ethyl-1-[3-methyl-4-(4,4,4- trifluoro-3-hydroxy-3-trifluoromethyl-(E)-but-1-enyl)-phenyl ]-propyl}-2-methyl- phenyl ester (compound prepared in Example 273-(2)) (30 mg, 0.05 mmol) in DMF (1 ml), PdCI2(UpPf)2-CH2CI2 (4 mg, 0.005 mmol), Et3N (0.024 ml, 0.17 mmol), CuI (10 mg, 0.05 mmol), and hex-5-ynoic acid methyl ester (14 mg, 0.1 mmol) were added at room temperature under nitrogen and stirred at 120 degrees C for 14 h. To the mixture, ethyl acetate was added and the mixture was washed with water and brine, dried over MgSO4, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (ethyl acetate/hexane =1/5) to give the title compound (18 mg, 61%) as colorless oil. 1H-NMR (CDCI3): 0.60 (t, 6H, J=7.3Hz), 1.55-1.70 (m, 2H), 1.72-1.90 (m, 2H), 2.06 (q, 4H, J=7.3Hz), 2.33 (s, 3H), 2.35 (s, 3H), 2.37 (t, 2H, J=7.1 Hz), 2.46 (t, 2H, J=6.9Hz), 3.16 (s, 1H), 3.67 (s, 3H), 6.08 (d, 1 H, J=16.1 Hz), 6.85-7.05 (m, 4H), 7.20-7.26 (m, 1H), 7.30-7.40 (m, 2H).

(2) Preparation of 7-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hyclroxy-3- trifluoromethyl^E^but-i-enyO-phenylJ-propylJ^-methyl-phenyO- hept-δ-ynoic acid

MeOOC HOOC

To a solution of 7-(4-{1 -Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-CEJ-but-i-enyO-phθnyll-propylJ^-methyl-phen yO-hept-β-ynoic acid methyl ester (compound prepared in Example 275-(1)) (18 mg, 0.031 mmol) in MeOH (1 ml), 1 N NaOH aq. (0.2 ml, 0.2 mmol) was added at room temperature and stirred at room temperature for 4 h. To the mixture, ethyl acetate was added and the mixture was washed with 30% NaHaPO4 aq., dried over MgSO4, concentrated in vacuo, and the obtained residue was chromatographed on silica gel (ethyl acetate/hexane =3/1) to give the title compound (13 mg, 74%) as colorless oil. 1H-NMR (CDCI3): 0.60 (t, 6H, J=7.2Hz), 1.60-1.75 (m, 2H), 1.76-1.90 (m, 2H), 2.06 (q, 4H, J=7.2Hz), 2.32 (s, 3H), 2.35 (s, 3H), 2.39 (t, 2H, J=7.4Hz), 2.47 (t, 2H, J=6.9Hz), 6.08 (d, 1 H, J=16.0Hz), 6.85-7.02 (m, 4H), 7.20-7.27 (m, 1 H), 7.30-7.40 (m, 2H);MS(ESI+): 569([M+H]+)

Example 276 Preparation of (R)-2-[2-(4-{1 -Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-acetylamino]- propionic acid (1) Preparation of (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxy)-acetic acid methyl ester

MeO _ OMOM OMOM CF3 CF3 Using the same procedure as described for the preparation of Example 203-(1 ), the title compound was prepared from 4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phe nyl]-propyl}-2- methyl-phenol (compound prepared in 30-(1)). 1H-NMR(CDCI3): 0.60 (t, 6H), 2.04 (q, 4H), 2.23 (s, 3H), 2.32 (s, 3H), 3.50 (s, 3H), 3.80 (s, 3H), 4.62 (s, 2H), 4.96 (s, 2H), 6.06 (d, 1 H), 6.57 (d, 1H), 6.88-7.05 (m, 4H), 7.30-7.38 (m ,2H)

(2) Preparation of (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxy)-acetic acid

MeO ,, OMOM O CF3 Using the same procedure as described for the preparation of Example 203-(2), the title compound was prepared from (4-{1 -Ethyl- 1-[3-methyl-4-((E)- 4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-eny l)-phenyl]-propyl}-2- methyl-phenoxy)-acetic acid methyl ester (compound prepared in 276-(1)). 1H-NMR(CDCI3): 0.56 (t, 6H), 2.01 (q, 4H), 2.15 (s, 3H), 2.28 (s, 3H), 3.48 (s, 3H), 4.46 (s, 2H), 4.94 (s, 2H), 6.04 (d, 1 H), 6.57 (d, 1 H), 6.85-7.01 (m, 4H), 7.28-7.37 (m, 2H)

(3) preparaton of (R)-2-[2-(4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hy droxy- 3-trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-pheno xy)-acetylamino]- propionic acid

Fmoc-D-Ala-Wang resin OMON Cr3

H HO rNτ or° Fmoc-D-Ala-Wang resin (0.54mmol/g as amino acid loading, 37.0 mg, 0.020mmol amino acid loading) was treated with 20% (v/v) piperidine in DMF (0.5ml) two times to deprotect Fmoc group and washed with DMF (1ml, 5 times). To the resin, solutions of (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-enyl)-phenyl]-propyl} -2-methyl- phenoxy)-acetic acid (prepared in Example 276-(2)) (16.3mg, 0.029mmol) in DMF (0.2ml), benzotriazole-1-yl-oxy-tris(dimethylamino)phosphonium hexafluorophosphate (17.7mg, 0.040mmol) in DMF (0.2ml) and N,N-diisopropyl ethyl amine (0.0105ml, 0.060mmol) in DMF (0.1ml) were added at room temperature, agitated at room temperature for 16h, filtrated, washed with DMF (2ml, 3 times), iPrOH (2ml, 3 times), THF (2ml, 3 times), MeOH (2ml, 3 times) and CH2CI2 (2ml, 3 times) and dried in vacuo. To the resin, 20% TFA in CH2CI2 (v/v) (1 ml) was added at room temperature, agitated at room temperature for 16h, filtrated, washed with CH2CI2 (1 ml, 2 times) and concentrated under vacuum to give the crude titled compound. MS (positive mode): 590 ([M+H∏ Example 277 Preparation of (R)-2-[2-(4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-acetylamino]- propionic acid

= O

(1) Preparation of (4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-pr opyl}-2-methyl-phenoxy)-acetic acid methyl ester

MeO CF3 O ,__OMOM CF3

Using the same procedure as described for the preparation of Example 203-(1), the title compound was prepared from 4-{1-Ethyl-1-[3-methyl-4-(4,4,4- trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phe nyl]-pro pyl}-2-methy!-phenol (compound prepared in 2-(2)). 1H-NMR(CDCI3): 0.59 (t, 6H), 2.04 (q, 4H)1 2.21 (s, 3H), 2.39 (s, 3H), 3.47 (s, 3H), 3.80 (s, 3H), 4.62 (s, 2H), 5.15 (s, 2H), 6.57 (s, 1H), 6.83-7.05 (m, 4H), 7.36 (d, 1 H)

(2) Preparation of (4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3- methoxymethoxy-3-trifluoromethyl-but-1-ynyl)-phenyl]-pr opyl}-2-methyl-phenoxy)-acetic acid MeO. CF3 . "OMOM OMOM CF3 CF3 Using the same procedure as described for the preparation of Example 200-(2), the title compound was prepared from (4-{1-Ethyl-1-[3-methyl- 4-(4,4,4-trifluoro-3-methoxymethoxy-3-trifluoromethyl-but-1- ynyl)-phenyl]-pr opyl}-2-methyl-phenoxy)-acetic acid methyl ester (compound prepared in 277-(I)). 1H-NMR(CDCI3): 0.59 (t, 6H), 2.04 (q, 4H), 2.16 (s, 3H), 2. 39 (s, 3H), 3.48 (s, 3H), 4.65 (s, 2H), 5.15 (s, 2H), 6.61 (d, 1 H), 6.85-7.05 (m, 4H), 7.37 (d, 1 H)

(3) preparaton of (R)-2-[2-(4-{1-Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydrox y-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-acetylamino]- propionic acid

Fmoc-D-Ala-Wang resin CF3 OMOM CF3

Using the same procedure as described for the preparation of Example 276-(3), the crude title compound was prepared from Fmoc-D-Ala-Wang resin and (4-{1 -Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-methoxymethoxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-pr opyl}-2-methyl-phenoxy)-acetic acid (compound prepared in 277-(2)) MS (positive mode): 588 ([M+H∏ Example 278 Preparation of (S)-2-[2-(4-{1-Ethyl-1 -[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy )-acetylamino]-3- phenyl-propionic acid

o

CF?H

Using the same procedure as described for the preparation of Example 276- (3), the crude title compound was prepared from Fmoc-L-Phe-Wang resin and (4-{1-Ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-methoxymeth oxy-3-trifluoromethyl- but-1-enyl)-phenyl]-propyl}-2-methyl-phenoxy)-acetic acid (compound prepared in 276-(2)) MS (positive mode): 666 ([M+H∏

Example 279 Preparation of (S)-2-[2-(4-{1 -Ethyl-1-[3-methyl-4-(4,4,4-trifluoro-3-hydroxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-propyl}-2-methyl-phenoxy )-acetylamino]-3- phenyl-propionic acid

o HO

Using the same procedure as described for the preparation of Example 276-(3), the crude title compound was prepared from Fmoc-L-Phe-Wang resin and (4-{1-Ethyl-1 -[3-methyl-4-(4,4,4-trifluoro-3-methoxymethoxy-3- trifluoromethyl-but-1-ynyl)-phenyl]-pr opyl}-2-methyl-phenoxy)-acetic acid (compound prepared in 277-(2)) MS (positive mode): 664 ([M+H]+) Example 280 3-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2- methyl-phenoxy)-propane-1 ,2-diol

Example 281 3-(4-{1-Ethyl-1-[4-(2-hydroxy-3,3-dimethyl-butyl)-3-methyl-p henyl]-propyl}-2- methyl-phenoxy)-propane-1 ,2-diol

OH

OH Example 282 (R)-3-(4-{1-Ethyl-1-[4-((R)-3-hydroxy-4,4-dimethyl-pentyl)-3 -methyl-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol

HO

Example 283 (S)-3-(4-{1-Ethyl-1-[4-((S)-3-hydroxy-4,4-dimethyl-pentyl)-3 -methyl-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol

OH

Example 284 (R)-3-(4-{1-Ethyl-1-[4-((S)-3-hydroxy-4,4-dimethyl-pentyl)-3 -methyl-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol OH

Example 285 (S)-3-(4-{1-Ethyl-1-[4-((R)-3-hydroxy-4,4-dimethyl-pentyl)-3 -methyl-phenyl]- propyl}-2-methyl-phenoxy)-propane-1 ,2-diol

OH

Example 286 (R)-3-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1 -enyl)-phenyl]-propyl}-2- methyl-phenoxy)-propane-1 ,2-diol

OH

Example 287 (S)-3-(4-{1 -Ethyl-1 -[4-((E)-3-hydroxy-4,4-dimethyl-pent-1 -enyl)-phenyl]-propyl}-2- methyl-phenoxy)-propane-1 ,2-diol

HO

Example 288 (R)-3-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-pheny l]-propyl}-2-methyl- phenoxy)-propane-1 ,2-diol OH

Example 289 (S)-3-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dinnethyl-pentyl)-phen yl]-propyl}-2-methyl- phenoxy)-propane-1 ,2-diol

OH Example 290 (S)-5-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-met hyl-phenyl]-propyl}-2- methyl-phenoxy)-pentane-1 ,4-diol

Example 291 4-(4-{1-Ethyl-1-[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl- phenyl]-propyl}-2- methyl-phenyl)-butane-1 ,2-diol

OH Example 292 4-(4-{1-Ethyl-1-[4-(2-hydroxy-3,3-dimethyl-butoxy)-3-methyl- phenyl]-propyl}-2- methyl-phenyl)-butane-1 ,2-diol

OH Example 293 1 -(4-{1 -Ethyl-1 -[4-(3-hydroxy-propyl)-3-methyl-phenyl]-propyl}-2-methyl- phenoxy)-3,3-dimethyl-butan-2-ol Example 294 1 -(4-{1 -Ethyl-1 -[4-(3-hydroxy-propyl)-3-methyl-phenyl]-propyl}-2-methyl-phe nyl)- 4,4-dimethyl-pentan-3-ol

Example 295 3-(4-{1-Ethyl-1-[4-(2-hydroxy-3,3-dimethyl-butoxy)-3-methyl- phenyl]-propyl}-2- methyl-phenyl)-butan-1 -ol

Example 296 (E)-4-(4-{1-Ethyl-1-[4-(2-hydroxy-3,3-dimethyl-butoxy)-3-met hyl-phenyl]-propyl}- 2-methyl-phenyl)-but-3-en-2-ol

OH Example 297 1 -(4-{1-Ethyl-1-[4-(3-hydroxy-butyl)-3-methyl-phenyl]-propyl} -2-methyl-phenoxy)- 3,3-dimethyl-butan-2-ol

Example 298 3-(4-{1 -Ethyl-1 -[4-(2-hydroxy-3,3-dimethyl-butoxy)-3-methyl-phenyl]-propyl} -2- methyl-phenyl)-propane-1 ,2-diol Example 299 3-(4-{1-Ethyl-1-[4-(2-hydroxy-3,3-dimethyl-butoxy)-3-methyl- phenyl]-propyl}-2- methyl-phenyl)-butane-1 ,2-diol

Example 300 1-(4-{1-[4-(2,3-Dihydroxy-propyl)-3-methyl-phenyl]-1-ethyl-p ropyl}-2-methyl- phenoxy)-3,3-dimethyl-butan-2-one

Example 301 1 -(4-{1 -[4-(2,3-Dihydroxy-1 -methyl-propyl)-3-methyl-phenyl]-1 -ethyl-propyl}-2- methyl-phenoxy)-3,3-dimethyl-butan-2-one

Example 302 1-(4-{1-[4-(1 ,2-Dihydroxy-propyl)-3-methyl-phenyl]-1 -ethyl-propyl}-2-methyl- phenoxy)-3,3-dimethyl-butan-2-one

OH

OH Example 303 1 -(4-{1 -Ethyl-1 -[4-(3-hydroxy-4,4-dimethyl-pentyl)-3-methyl-phenyl]-propyl} -2- methyl-phenyl)-4,4-dimethyl-pentan-3-ol OH OH

The following compounds are prepared in accordance with the procedure described as in the above Examples.

Example 304 Preparation of (R)-5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1-methyl-cyclopentyl)-prop-1 ■ ynyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dihyd ro-furan-2-one

Example 305 Preparation of 5-[4-(1 -Ethyl-1 -{4-[3-hydroxy-3-(1 -methyl-cyclopentyl)-prop-1 - ynyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxy]-4(R)-hydrox y-pentanoic acid

OH

Example 306 Preparation of (R)-5-[4-(1 -ethyl-1 -{4-[3-hydroxy-3-(1 -methyl-cyclopentyl)-propyl]- 3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dihydro-fur an-2-one

OH (1) Preparation of 1-methyl-cyclopentanecarboxylic acid N-methoxy-N-methyl- amide

To a solution of N,O-dimethylhydroxylamine hydrochloride (594.5 mg, 6.09 mmol) in THF (4 ml) was added 2.67M n-butyl lithium in hexane (4.10 ml, 10.95 mmol) dropwise at -78 degrees C, and the mixture was stirred at room temperature for 10 min. The mixture was cooled to -78 degrees C, and 1-methyl- cyclopentanecarboxylic acid methyl ester (430.5 mg, 3.03 mmol) in THF (2 ml) was added dropwise to the mixture. After stirring at -78 degrees C for 1h 45min, diethyl ether was added, and the solution was washed with sat.NH4CI aq. and brine, dried over MgSO4, filtered, concentrated in vacuo, and chromatographed (ethyl acetate/hexane = 0/100 to 15/85) to give the title compound (154.2 mg, 30 %). 1 H-NMR (CDCI3): 1.23 (s, 3H), 1.55-1.66 (m, 6H), 2.03-2.08 (m, 2H), 3.18 (s, 3H), 3.66 (S, 3H); MS(ESI+): 172([M+H]+).

(2) Preparation of 3-(4-{1-[4-(tert-butyl-dimethyl-silanyloxy)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenyl)-1 -(1-methy!-cyclopentyl)-prop-2-yn-1 -one

TBSO^T ^^^ Jb ^J TBS0 o To a solution of tert-butyl-{4-[1-ethyl-1-(4-ethynyl-3-methyl-phenyl)-propyl] -2- methyl-phenoxy}-dimethyl-silane (compound prepared in Example 260-(2)) (434.1 mg, 1.07 mmol) in THF (3 ml), 2.67 M n-butyl lithium in hexane (0.420 ml, 1.12 mmol) was added at -78 degrees C. To the mixture, 1-methyl- cyclopentanecarboxylic acid N-methoxy-N-methyl-amide (compound prepared in Example 306-(1)) (151.9 mg, 0.887 mmol) in THF (2 ml) was added at -78 degrees C, stirred at -78 degrees C to room temperature for 2.5 h. The mixture was poured into brine and extracted with ethyl acetate. Organic layer was washed with brine, dried over MgSO4, filtered, concentrated in vacuo, and chromatographed (ethyl acetate/hexane = 0/100 to 2/98) to give the title compound (434.9 mg, 95 %). 1 H-NMR (CDCI3): 0.19 (s, 6H), 0.58 (t, 6H, J=7.3Hz), 0.99 (s, 9H), 1.32 (s, 3H), 1.42-1.51 (m, 2H), 1.69-1.74 (m, 4H), 2.03 (q, 4H, J=7.2Hz), 2.14 (s, 3H)1 2.24- 2.32 (m, 2H), 2.44 (s, 3H), 6.63 (d, 1 H, J=8.4Hz), 6.79 (dd, 1 H, J=8.4, 2.0Hz), 6.84 (s, 1H), 7.00 (d, 1H, J=8.9Hz), 7.05 (s, 1H), 7.41 (d, 1H, J=8.1 Hz); MS(ESI+): 517([M+H]+).

(3) Preparation of 4-(1 -ethyl-1 -{4-[3-hydroxy-3-(1 -methyl-cyclopentyl)-prop-1 - ynyl]-3-methyl-phenyl}-propyl)-2-methyl-phenol

TBSO I I O OH To a solution of 3-(4-{1-[4-(tert-butyl-dimethyl-silanyloxy)-3-methyl-phenyl] -1- ethyl-propyl}-2-methyl-phenyl)-1 -(1 -methyl-cyclopentyl)-prop-2-yn-1 -one (compound prepared in Example 306-(2)) (432 mg, 0.835 mmol) in MeOH (3 ml) and THF (8 ml), NaBH4 (155.5 mg, 4.11 mmol) was added at room temperature, stirred at room temperature for 30 min. Ethyl acetate was added. The solution was washed with brine, dried over MgSO4, concentrated in vacuo. The residue was dissolved to THF (16 ml), and 1M terabutylammonium fluoride in THF (0.880 ml, 0.880 mmol) was added at -10 degrees C. The mixture was stirred for 5 min. Ethyl acetate was added. The solution was washed with brine, dried over MgSO4, concentrated in vacuo, and purified by preparative TLC (ethyl acetate/hexane = 0/100 to 25/75) to give the title compound (352 mg, quant.). 1 H-NMR (CDCI3): 0.58 (t, 6H, J=7.3Hz), 1.14 (s, 3H), 1.37-1.44 (m, 2H), 1.57- 1.80 (m, 6H), 1.82 (d, 1 H, J=5.9Hz), 2.02 (q, 4H, J=7.3Hz), 2.18 (s, 3H), 2.36 (s, 3H), 4.38 (d, 1 H, J=5.9Hz), 4.51 (s, 1 H), 6.63 (dd, 1H, J=8.8, 1.5Hz), 6.81-6.85 (m, 2H), 6.92 (dd, 1H, J=8.1 , 1.6Hz), 6.98 (s, 1H), 7.27 (d, 1H, J=8.3Hz); MS(ESI+): 405([M+H]+). (4) Preparation of (R)-5-[4-(1-ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopentyl)- propyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dih ydro-furan-2-one

OH o OH O To a solution of 4-(1-ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopentyl)-prop-1-y nyl]- 3-methyl-phenyl}-propyl)-2-methyl-phenol (compound prepared in Example 306- (3)) (140 mg, 0.346 mmol) in MeOH (15 ml), 10%Pd/C (31.1 mg) was added. The mixture was stirred at room temperature for 16 h under hydrogen. The mixture was filtered, concentrated in vacuo. To the residue in N1N- dimethylacetamide (5 ml), K2CO3 (194 mg, 1.40 mmol) and (R)-(-)-dihydro-5-(p- tolylsulfonyloxymethyl)-2(3H)-furanone (152 mg, 0.562 mmol) were added. The mixture was stirred at 90 degrees C for 27 h. After cooled to room temperature, (R)-(-)-dihydro-5-(p-tolylsulfonyloxymethyl)-2(3H)-furanone (10.2 mg, 0.0377 mmol) was added. The mixture was stirred at 90 degrees C for 6.5 h. After cooled to room temperature, brine was added, extracted with ethyl acetate. The organic layer was washed with brine, dried over MgSO4, concentrated in vacuo, and chromatographed (ethyl acetate/hexane = 0/100 to 40/60) to give the title compound (109.1 mg, 62 %). 1 H-NMR (CDCI3): 0.58 (t, 6H, J=7.3Hz), 0.90 (s, 3H), 1.23-1.40 (m, 4H), 1.49- 1.73 (m, 6H), 2.03 (q, 4H, J=7.2Hz), 2.14 (s, 3H), 2.25 (s, 3H), 2.28-2.62 (m, 4H), 2.71-2.87 (m, 2H), 3.30-3.34 (m, 1 H), 4.11 (ddd, 2H, J=28.2, 8.4, 3.29Hz), 4.85-4.90 (m, 1H), 6.65 (d, 1H1 J=8.4Hz), 6.88-7.03 (m, 5H); MS(ESI-): 505([M- H]").

Example 307 Preparation of 5-[4-(1 -Ethyl- 1 -{4-[3-hydroxy-3-(1 -methyl-cyclopentyl)-propyl]-3- methyl-phenyl}-propyl)-2-methyl-phenoxy]-4(R)-hydroxy-pentan oic acid OH

To a solution of (R)-5-[4-(1-ethyl-1-{4-[3-hydroxy-3-(1-methyl-cyclopentyl)- propyl]-3-methyl-phenyl}-propyl)-2-methyl-phenoxymethyl]-dih ydro-furan-2-one (compound prepared in Example 306-(4)) (105.7 mg, 0.209 mmol) in MeOH (10 ml) and THF (10 ml), 1N NaOH solution (2 ml) was added. The mixture was stirred at room temperature for 2 h. The mixture was concentrated in vacuo and purified by preparative TLC (CHCI3/MeOH = 8/3 saturated with H2O) to give the title compound (86.1 mg, 79 %). 1 H-NMR (CDCI3): 0.58 (t, 6H, J=7.2Hz), 0.89 (s, 3H), 1.20-1.80 (m, 10H), 1.87- 1.93 (m, 2H), 2.03 (q, 4H, J=7.2Hz), 2.16 (s, 3H), 2.25 (s, 3H), 2.50-2.63 (m, 3H), 2.79-2.90 (m, 1 H), 3.33 (dd, 1 H, J=10.0, 1.6Hz), 3.83 (dd, 1 H, J=9.6, 6.8Hz), 3.95 (dd, 1 H, J=9.6, 3.5Hz), 4.00-4.10 (m, 1 H), 6.66 (d, 1 H, J=8.3Hz), 6.88-6.95 (m, 4H), 7.01 (d, 1 H, J=8.4Hz); MS(ESI-): 523([M-H]").

Example 308 Preparation of (S)-6-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3 - methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-tetrahydro-py ran-2-one

Preparation of (S)-6-(4-{1 -Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-tetrahydro-py ran-2-one To a solution of 4-{1-ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3-methyl - phenyl]-propyl}-2-methyl-phenol (compound prepared in Example 1-(5)) (50mg, 0.131 mmol), PPh3 (103mg, 0.394mmol), (S)-6-hydroxymethyl-tetrahydro-pyran- 2-one (J. Chem. Soc, Perkin Trans. 1, 2000, 20, 3519.) (51mg, 0.394mmol) in THF (0.2ml), DEAD (69mg, 0.394mmol) was added slowly at room temperature and stirred at room temperature for 37 h. The mixture was concentrated in vacuo and chromatographed (n-hexane/ethyl acetate =1/3 developed once, n- hexane/ethyl acetate =3/1 developed once, n-hexane/ethyl acetate =1/1 developed once) to give the title compound (5.3mg, 8.2%). MS(positive): 510([M+NH4]+).

Example 309 Preparation of (S)-6-(4-{1 -Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-pent-1 -enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid

o OH

Preparation of (S)-6-(4-{1-Ethyl-1 -[4-((E)-3-ethyl-3-hydroxy-ρent-1-enyl)-3- methyl-phenyl]-propyl}-2-methyl-phenoxy)-5-hydroxy-hexanoic acid

To a solution of (S)-6-(4-{1-Ethyl-1-[4-((E)-3-ethyl-3-hydroxy-pent-1-enyl)-3 - methyl-phenyl]-propyl}-2-methyl-phenoxymethyl)-tetrahydro-py ran-2-one (compound prepared in Example 308) (0.53mg, 0.001 mmol) in THF (0.05ml) and , MeOH (0.05ml), 1 N KOH aq (0.05ml, O.Oδmmol) was added at rt and stirred at 60 degrees C for 12 h. The mixture was extracted with ethyl acetate, dried over MgSO4, filtered, concentrated in vacuo to give the title compound. MS(positive): 493([M-OH]+), MS(negative): 509([M-H]-). Test Example Biological activities

Preparation of tested compounds 1 ,25(OH)2D3 was purchased from Solvay Pharmaceuticals (Weesp, The Netherlands). LG190178 (the compound disclosed in WO00/10958 and the corresponding U.S. Patent 6,218,430 B1) was prepared in accordance with the procedure described as the said patent specification (Example 10). Compound A, B1 C, and D (the compounds disclosed in WO03/101978A1 ) were prepared in accordance with the procedure described as the said patent specification (Example 110 and its diastereomers). The compounds of the present invention were prepared as exemplified above. The chemical structure of LG190178 is as follows:

OH The chemical structure of compound A is as follows:

HOOC

The chemical structure of compound B (epimer of compound A) is as follows:

HOOC

The chemical structure of compound C is as follows:

/-NH HOOC

The chemical structure of compound D (epimer of compound C) is as follows: HOOC

Test Example 1 PTH Production From Bovine Parathyroid Cells

Preparation of parathyroid cells Fresh bovine parathyroid glands obtained from a slaughterhouse were transported to the laboratory in ice-cold DMEM/F-12 (GIBCO BAL, NY, USA) containing antibiotic-antimycotic (GIBCO BAL). The parathyroid glands were trimmed of excess fat and connective tissue with scissors and sliced with the slicer. They were minced finely (not more than 1 mm fragments) and suspended in digestion medium consisting of DMEM/F-12 (10 ml digestion medium/1 g parathyroid tissue) containing 2 mg/ml collagenase (Wako Pure Chemical Industries, Ltd., Osaka, Japan), 40 mg/ml deoxyribonuclease Il (SIGMA-ALDRICH Co., St. Louis MO, USA), and antibiotics (penicillin, streptomycin). The mixture was incubated at 37 °C with shaking (120 strokes/min.) for 120-180 min. to disperse the cells. The turbid solution was then filtered through nylon mesh (70 μm cell strainer) and centrifuged at 1100 rpm. (240 x g) for 10 min. at 4 °C. The pellet was resuspended and washed twice in DMEM/F-12. The pellet was finally resuspended in DMEM/F-12 containing 10 % fetal bovine serum (FBS) and aliquots were taken for cell counting.

Parathyroid cell cultures The dispersed cells were plated in 96-well plate at a concentration of 2 x 104 cells/well and incubated for 2 days at 37 °C. The culture medium was then replaced with the same medium containing various concentrations of 1 ,25(OH)2D3 (as a positive control), LG190178 (the compound disclosed in WO00/10958 and the corresponding U.S. Patent 6,218,430 B1) or the compounds of the present invention, and cells were cultured for 3 days at 37 °C. To determine the rate of PTH secretion, the cells were washed once with DMEM/F-12 (FBS free), and then incubate for 4 hr. in fresh FBS free medium at 37 °C. The medium were collected and frozen at -30 °C until assay for the concentration of PTH.

Radio immuno assay of PTH in the medium PTH concentration in the culture media was determined using the PTH assay kit YAMASA RIA kit available from YAMASA Co., (Chiba, Japan).

Comparison of inhibitory activity on PTH release in parathyroid cells The 50 % inhibitory concentration (IC50) values were determined from the PTH concentrations. The inhibitory activity was calculated as the ratio of the IC50 value of the compounds to that of 1 ,25(OH^D3. The results are shown in the following Table 2. The relationship between the diseases and the inhibitory activity on PTH release in parathyroid cells is described in Am J Kidney Pis. 1995 Nov:26(5):852-60 for example.

Test Example 2 The mRNA expression assay of ECAC2 in Caco-2 cells

Caco-2 cell cultures The dispersed cells were plated in 48-well plate at a concentration of 6.3 x 104 cells/well and incubated for 4 days at 37 °C. The culture medium (Dulbecco's Modified Eagle Medium (D-MEM) without NaHCO3 with 44 mM NaHCO3, 1 mM non-essential amino acids, and 2 mM L-glutamine, 90%; fetal bovine serum, 10%) was then replaced with the same medium containing various concentrations of LG190178 (the compound disclosed in WO00/10958 and the corresponding U.S. Patent 6,218,430 B1) or the compounds of the present invention, and cells were cultured for 1 day at 37 °C. The culture medium containing the compounds was changed twice per day. Total RNA isolation from Caco-2 cell Total RNA was isolated from Caco-2 cell following ABI PRISM™ 6100 Nucleic Acid PrepStation protocol from Applied Biosystems.

Real time RT-PCR assay of ECAC2 ECAC2 mRNA expression was determined using TaqMan One-step RT-PCR Master Mix Reagents Kit and PRISM7000 systems from Applied Biosystems. Primer information and cycle conditions are 1)ECAC2, forward 5'- CCTTCACCATCATGATTCAGAAG-S1, reverse 5'- GTCCTCTGTCTGGAAGATGA-S', Taqman probe 51- TTCTGCTGGCTGATGGCTGTGGTC-S', 55 cycles, annealing temperature (Ta) = 600C; 2)GAPDH, forward 5'-GAAGGTGAAGGTCGGAGTC-31l reverse 51-GAAGATGGTGATGGGATTTC-3ll Taqman probe 5- CAAGCTTCCCGTTCTCAGCC-S1, 55 cycles, Ta = 600C. ECAC2 mRNA values were normalized for the expression of GAPDH mRNA within each sample.

Comparison of ECAC2 mRNA value The EC50 values of ECAC2 mRNA values were analyzed by Emax models. The ECAC2 mRNA ratio was calculated as the ratio of the EC50 value of the compounds to that of LG190178. The results are shown in the following Table 4. ECAC2 is a channel-like transporter mediating intestinal calcium absorption. It is described in J Biol Chem. 1999 Aua 6:274(32):22739-46 for example.

Test Example 3

MG-63 Osteocalcin Induction Assay

Preparation of MG-63 Cells

RECTIFIED SHEET (RULE 91) ISA/EP MG-63 cells were cultured in MEM (minimum essential medium) medium (pH 7.0) (Invitrogen Corp., Carlsbad, CA, USA) containing 5% fetal bovine serum (FBS) (Hyclone, Logan, UT, USA) before assay. MG-63 cells were detached by Trypsin-EDTA solution and resuspended in MEM medium. Cell density was adjusted to 4.0 x 104 cells/mL with the MEM medium and 0.2 ml_ of the cells was seeded onto each well of 96-well plate. The cells were incubated at 37 °C in 5% CO2 for 24 hours.

MG-63 Cells Culture The cells were washed once with 200 micro L of MEM medium containing 5% of DCC-FBS. Then, the 180 micro L of MEM medium containing 5% dextran/charcoal-treated FBS (DCC-FBS) were added onto each well of 96-well plate. 1 ,25(OH)2D3 was purchased from Solvay Pharmaceuticals (Weesp, The Netherlands) and was used for standard. Test compounds were diluted to 1.0 x 10-3 mol/L, 1.0 x 10"4 mol/L, 1.0 x lO"5 mol/L, 1.0 x lO'6 mol/L, 1.0 x 10"7 mol/L and 1.0 x 10"8 mol/L with DMSO. These compounds solutions were stored at -20 °C until use. MG-63 cells were treated with these compounds (20 micro L) at final concentration of 1.0 x 10"6 mol/L, 1.0 x 10"7 mol/L, 1.0 x 10"8 mol/L, 1.0 x 10"9 mol/L, 1.0 x 10"10 mol/L and 1.0 x 10"11 mol/L in MEM medium containing 5% DCC-FBS. The plate was mixed gently and incubated at 37 °C and 5% CO2 for 8 hours. The final concentration of DMSO was less than 0.1 %. After the incubation, cultured medium were removed and 200 micro L of MEM containing 5% DCC-FBS were added onto each well of 96-well plate. The cells were incubated at 37 0C and 5% CO2 for 4 days. After 4 days culture, 150 micro L of supernatant was collected into new 96-well plate and stored at -80 °C.

Enzyme Immunoassay of Osteocalcin Osteocalcin concentration of supernatant was determined by Gla-type osteocalcin EIA kit (Takara Bio. Inc., Tokyo, Japan). Frozen supernatant was thawed slowly with shaking gently at room temperature prior to use. The absorbance was measured at 450 nm with a microplate reader (Model 3550, Bio-Rad Laboratories, Hercules, CA, USA). Each concentration was calculated by comparison with standards using Microplate Manager III software (Bio-Rad Laboratories).

Comparison of induction activity on osteocalcin in M6-63 cells The 50 % effect concentration (ECso) values were determined from the osteocalcin concentrations. The inductive activity was calculated as the. ratio of the EC50 value of the compounds to that of 1 ,25(OH)2D3. The results are shown in the following Table 3. The relationship between the diseases and the induction activity on osteocalcin is suggested in Lancet (1984 May 19). 1(83861 1091-3. Steroids 66. 159-170 (2001) or Journal of Steroid Biochemistry & Molecular Biology 89-90. 269-271 (2004) for example.

Test Example 4 Bone mineral density in the ovariectomized (QVX) rats (1 )

Reagents The compounds of the present invention were prepared as exemplified above, dissolved in a vehicle (medium chain triglyceride, MCT) and diluted to a given concentration. The stock solutions were protected from light and stored at 4 0C.

Animals Eight-moπth-old female Sprague-Dawley (Crl:CD(SD)) rats were purchased from Charles River Japan Inc. (Kanagawa, Japan) and acclimated under standard laboratory conditions at 24 ± 2 0C and 50-60% humidity. The rats were allowed free access to tap water and commercial standard rodent chow CE-2 (Clea Japan Inc., Japan).

Experimental design

RECTIFIED SHEET (RULE 91) ISA/EP Sham-operated (n = 8) and the ovariectomized (OVX) rats were used. The OVX rats were divided into each group (n = 8) one day after the surgery. In the sham and OVX control groups, rats received the vehicle (MCT) p.o. at a dose of 1 ml/kg body weight (BW) five times a week. Each compound was given orally five times a week for 4 weeks. These animal studies were carried out in accordance with Chugai Pharmaceutical's ethical guidelines for animal care, and the experimental protocols were approved by the animal care committee of the institution. During the 24 hours from the last administration, urine was collected with metabolic cage, and blood was drawn from the abdominal aorta under ether anesthesia. Blood and urine samples were centrifuged to obtain the supernatant, which were stored at -20 °C until assay. The lumbar vertebrae and femur were removed. The lumbar vertebra and the right femur were stored in 70% ethanol at 4 0C for the measurement of bone mineral density (BMD).

Serum and urine biochemistry Serum calcium (Ca) and inorganic phosphorus (Pi) concentrations were measured with an autoanalyzer (Hitachi 7170, Tokyo, Japan). The serum osteocalcin concentration was measured with Osteocalcin rat ELISA system (Amersham Pharmacia Biotech, Tokyo, Japan). Urinary Ca, Pi, and creatinine (Cre) were measured with an autoanalyzer. Urinary deoxypyridinoline (D-Pyr) was measured using a Metra DPD EIA kit (Quidel Co., USA), and the data were corrected for urinary Cre concentrations.

Measurement of bone mineral density The second through fourth lumbar vertebaral (L2-L4) BMD (mg/cm2) and femoral BMD were measured by dual-energy X-ray absorptiometry (DCS-600-EX, Aloka, Japan). The results are shown in the following Table 5. Test Example 5 Bone mineral density in the ovariectomized (OVX) rats (2) Reagents Alfacalcidol was synthesized in Chugai Pharmaceutical Co., Ltd., Japan, dissolved in a vehicle (medium chain triglyceride, MCT) and diluted to a given concentration. The stock solutions were protected from light and stored at 4 °C.

Animals Eight-month-old female Sprague-Dawley (Crl:CD(SD)) rats were purchased from Charles River Japan Inc. (Kanagawa, Japan) and acclimated under standard laboratory conditions at 23 ± 2 0C and 40-70% humidity. The rats were allowed free access to tap water and commercial standard rodent chow CRF-1 (Oriental Yeast Co. Ltd., Japan).

Experimental design Sham-operated (n = 8) and the ovariectomized (OVX) rats were used. The OVX rats were divided into each group (n = 8) one day after the surgery. In the sham and OVX control groups, rats received the vehicle (MCT) p.o. at a dose of 1 ml/kg body weight (BW) every day. Each compound was given orally seven times a week for 4 weeks. During the 24 hours from the last administration, urine was collected with metabolic cage, and blood was drawn from the jugular vein under ether anesthesia. Blood and urine samples were centrifuged to obtain the supernatant, which were stored at -20 °C until assay. The lumbar vertebrae and femora were removed. The lumbar vertebra and the right femur were stored in 70% ethanol at 4 0C for the measurement of bone mineral density (BMD).

Serum and urine biochemistry Serum calcium (Ca) and inorganic phosphorus (Pi) concentrations were measured with an autoanalyzer (Hitachi 7170, Tokyo, Japan). The serum osteocalcin concentration was measured with Osteocalcin rat ELISA system (Amersham Pharmacia Biotech, Tokyo, Japan). Urinary Ca, Pi, and creatinine (Cre) were measured with an autoanalyzer. Urinary deoxypyridinoline (D-Pyr) was measured using a Metra DPD EIA kit (Quidel Co., USA), and the data were corrected for urinary Cre concentrations.

Measurement of bone mineral density The second through fifth lumbar vertebaral (L2-L5) BMD (mg/cm2) and femoral BMD were measured by dual-energy X-ray absorptiometry (DCS-600-EX, Aloka, Japan). The results are shown in the following Table 6.

Table 2 Example No Inhibitory activity on PTH release in parathyroid cells (%) 1 332 2 431 27 105 30 1688 31 268 49 387 52 617 54 170 56 546 59 485 60 312 62 1990 69 931 77 119 78 765 79 139 84 618 88 111 92 251 106 157 107 734 115 150 154 178 156 400 157 175 170 105 192 182 1,25(OH)2D3 100 LG190178 2 CompoundA 3 CompoundB 1 CompoundC 1 CompoundD 1

Table3 Example No Osteocalcin production activity in MG-63 cells (%) 447 546 27 302 ~28~ 427 ~30~ 3746 429 !Ϊ5~ 1317 ~37~ 238 44 282 48 919 49 1718 52 5219 54 119 55 1288 56 10747 57 341 59 1281 60 1464 61 14230 62 2677 64 807 66 337 67 556 68 1078 69 4906 72 350 75 363 77 1003 78 4571 79 329 80 368 81 454 84 3371 86 271 88 458 92 402 102 856 106 159 107 471 115 173 119 906 121 248 125 618 140 277 141 73 147 241 152 581 153 796 154 4289 155 444 156 4747 157 1959 165 231 166 1344 167 1037 169 3771 170 2164 186 888 187 2176 190 616 192 289 195 530 198 462 1,25(OH)2D3 100 LG190178 185 CompoundA 67 CompoundB 3 CompoundC 43 CompoundD 4

Table 4 Example No ECaC-2 mRNA induction activity in Caco-2 cells (%) 1 36 2 49 27 114 28 2093 30 1777 31 161 35 538 37 639 44 96 48 519 49 987 52 1227 54 172 55 662 56 276 57 24 59 117 60 235 61 918 62 410 64 90 66 126 67 860 68 355 69 > 10000 72 542 75 309 77 534 78 6659 79 178 80 518 81 102 84 1843 86 289 88 845 92 226 102 166 106 399 107 823 115 91 119 12 121 75 125 <10 140 53 141 31 147 75 152 586 153 1662 154 1784 155 86 156 4760 157 1647 165 2017 166 86 167 323 170 191 186 57 187 545 190 22 192 292 195 135 198 271 1 ,25(OH)2D3 556 LG190178 100 Compound A 123 Compound B 15 Compound C 34 Compound D 14

Table 5 Spinal S.E. serum Ca S.E. BMD mg/dL mg/cm2 SHAM 185.8 4.8 10.4 0.1 OVX 166.8 4.3 10.0 0.1 Example 140 compound 186.6 5.6 10.0 0.1 0.75 microgram/kg/week Example 141 compound 184.4 2.5 10.1 0.1 7.5 microgram/kg/week

Table 6 Spinal S.E. serum Ca S.E. BMD mg/dL mg/cm2 SHAM 189.5 3.9 10.7 0.1 OVX 176.6 4 10.2 0.1 Alfacalcidol 182.1 4.5 10.2 0.1 0.125microgram/kg/week Alfacalcidol 180.9 3.7 10.6 0.1 0.25microgram/kg/week Alfacalcidol 185.1 3.8 10.7 0.2 0.5microgram/kg/week

It is understood that the foregoing detailed description and accompanying examples are merely illustrative and are not to be taken as limitations upon the scope of the invention, which is defined solely by the appended claims and their equivalents. Various changes and modifications to the disclosed embodiments will be apparent to those skilled in the art. Such changes and modifications, including without limitation those relating to the chemical structures, substituents, derivatives, intermediates, syntheses, formulations and/or methods of use of the invention, may be made without departing from the spirit and scope thereof.