SUBSTITUTED PHENYL SULFONAMIDES AS SELECTIVE β3

AGONISTS FOR THE TREATMENT OF DIABETES AND OBESITY

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation-in-part of our copending application Serial Number 08/015689 filed February 9, 1993.

BACKGROUND OF THE INVENTION β-Adrenoceptors have been subclassified as β 1 and β2 since 1967. Increased heart rate is the primary consequence of βl -receptor stimulation, while bronchodilation and smooth muscle relaxation typically result from β2 stimulation. Adipocyte lipolysis was initially thought to be solely a βl -mediated process. However, more recent results indicate that the receptor-mediating lipolysis is atypical in nature. These atypical receptors, later called β3-adrenoceptors, are found on the cell surface of both white and brown adipocytes where their stimulation promotes both lipolysis (breakdown of fat) and energy expenditure.

Early developments in this area produced compounds with greater agonist activity for the stimulation of lipolysis (β3 activity) than for stimulation of atrial rate (βl ) and tracheal relaxtion (β2). These early developments disclosed in Ains worth et ah, U.S. Patents 4,478,849 and 4,396,627, were derivatives of phenylethanolamines.

Such selectivity for β3-adrenoceptors could make compounds of this type potentially useful as antiobesity agents. In addition, these compounds have been reported to show antihypergly- cemic effects in animal models of non-insulin-dependent diabetes mellitus.

A major drawback in treatment of chronic diseases with β agonists is the potential for stimulation of other β-receptors and subsequent side effects. The most likely of these include muscle tremor (β2) and increased heart rate (βl ). Although these phenylethanolamine derivatives do possess some β3 selectively, side effects of this type have

been observed in human volunteers. It is reasonable to expect that these side effects resulted from partial βl and/or β2 agonism.

More recent developments in this area are disclosed in Ainsworth et al, U.S. Patent 5,153,210, Caulkett et al-, U.S. Patent 4,999,377, Alig et ah, U.S. Patent 5,017,619, Lecount et ah, European Patent 427480 and Bloom et l, European Patent 455006.

Even though these more recent developments purport to describe compounds with greater β3 selectively over the β 1 and β2 activities, this selectively was determined using rodents, in particular, rats as the test animal. Because even the most highly selective compounds, as determined by these assays, still show signs of side effects due to residual β l and β2 agonist activity when the compounds are tested in humans, it has become apparent that the rodent is not a good model for predicting human β3 selectivity.

Recently, assays have been developed which more accurately predict the effects that can be expected in humans. These assays utilize cloned human β3 receptors which have been expressed in Chinese hamster ovary cells. The agonist and antagonist effects of the various compounds on the cultivated cells provide an indication of the antiobesity and antidiabetic effects of the compounds in humans.

SUMMARY OF THE INVENTION

The instant invention is concerned with substituted phenyl sulfonamides which are useful as antiobesity and antidiabetic compounds. Thus, it is an object of this invention to describe such compounds. It is a further object to describe the specific preferred stereoisomers of the substituted phenylsulfonamides. A still further object is to describe processes for the preparation of such compounds. Another object is to describe methods and compositions which use the compounds as the active ingredient thereof. Further objects will become apparent from reading the following description.

DESCRIPTION OF THE INVENTION

The compounds of the instant invention are best realized in the following structural formula:

I

where n is 0 to 7; m is 0 or 1 ; r is 0 to 3;

A is phenyl, naphthyl, a 5 or 6-membered heterocyclic ring with from 1 to 4 heteroatoms selected from oxygen, sulfur or nitrogen, a benzene ring fused to a C3-C8 cycloalkyl ring, a benzene ring fused to a 5 or 6-membered heterocyclic ring with from 1 to 3 heteroatoms selected from oxygen, sulfur or nitrogen or a 5 or 6-membered heterocyclic ring with from 1 to 3 heteroatoms selected from oxygen, sulfur or nitrogen fused to a 5 or 6- membered heterocyclic ring with from 1 to 3 heteroatoms selected from oxygen, sulfur or nitrogen;

Rl is hydroxy, oxo, halogen, cyano, nitro, NR8R8 ₅ SR8, trifluoromethyl, C1 -C6 alkyl, -C6 alkoxy, C3-C8 cycloalkyl, phenyl, S02R9, NR8COR9, COR9, NR8SO2R ⁹ , NR CO2R8 or C1 -C6 alkyl substituted by hydroxy, nitro, halogen, cyano, NR8R8, SR8, trifluoromethyl, -C6 alkoxy, C3-C8 cycloalkyl, phenyl, NR8COR9, COR9, S02R9, NR8S02R9, NR8CO2R8, or Rl is a 5 or 6- membered heterocycle with from 1 to 3 heteroatoms selected from oxygen, sulfur or nitrogen;

R2 and R3 are independently hydrogen, Cl -C6 alkyl or Cl -C6 alkyl substituted by 1 to 3 of hydroxy, C1 -C6 alkoxy, or halogen;

X is -CH2-, -CH2-CH2- , -CH=CH- or -CH2O-;

R4 and R5 are independently hydrogen, C1 -C6 alkyl, halogen, NHRg,

R6 is hydrogen or Cl -C6 alkyl;

R7 is C 1 -C6 alkyl, C3-C8 cycloalkyl, or B-(R 1 ) _n ;

B is phenyl, naphthyl, a 5 or 6-membered heterocyclic ring with from 1 to 4 heteroatoms selected from oxygen, sulfur or nitrogen, a benzene ring fused to a C3-C8 cycloalkyl ring, a benzene ring fused to a 5 or 6-membered heterocyclic ring with from 1 to 3 heteroatoms selected from oxygen, sulfur or nitrogen or a 5 or 6-membered heterocyclic ring with from 1 to 3 heteroatoms selected from oxygen, sulfur or nitrogen fused to a 5 or 6- membered heterocyclic ring with from 1 to 3 heteroatoms selected from oxygen, sulfur or nitrogen;

R8 is hydrogen, Cl -Cio alkyl, C3-C8 cycloalkyl, phenyl optionally substituted by 1 to 3 of halogen, C1 -C6 alkyl or C1 -C6 alkoxy, or Cl -ClO alkyl substituted by 1 to 3 of hydroxy, halogen, CO2H, CO2-C1-C6 alkyl, C3-C8 cycloalkyl, C1-C6 alkoxy, or phenyl optionally substituted by from 1 to 3 of halogen, C1 -C6 alkyl or C1-C6 alkoxy;

R9 is R8, NHR8 or NR8R8.

In the above structural formula and throughout the instant specification, the following terms have the indicated meanings:

The alkyl groups specified above are intended to include those alkyl groups of the designated length in either a straight or branched configuration. Exemplary of such alkyl groups are methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, tertiary butyl, pentyl, isopentyl, hexyl, isohexyl, and the like.

The alkoxy groups specified above are intended to include those alkoxy groups of the designated length in either a straight or

branched configuration. Exemplary of such alkoxy groups are methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, tertiary butoxy, pentoxy, isopentoxy, hexoxy, isohexoxy and the like.

The term "halogen" is intended to include the halogen atoms fluorine, chlorine, bromine and iodine.

Certain of the above defined terms may occur more than once in the above formula and upon such occurrence each term shall be defined independently of the other.

The preferred 5 and 6-membered heterocycles and fused heterocycles of A, B and Rl are those heterocycles with from 1 to 4 heteroatoms independently selected from one of oxygen or sulfur or 1 to 4 nitrogen atoms.

The preferred values of A and B are phenyl, naphthyl or the foregoing preferred 5 and 6-membered heterocycles and fused heterocycles.

The more preferred values of A are phenyl, naphthyl, pyridyl, quinolinyl, pyrimidinyl, pyrrollyl, thienyl, imidazolyl, and thiazolyl.

The more preferred values of B are phenyl, naphthyl, quinolinyl, thienyl, benzimidazolyl, thiadiazolyl, benzothiadiazolyl, indolyl, indolinyl, benzodioxolyl, benzodioxanyl, benzothiophenyl, benzofuranyl, benzisoxazolyl, benzothiazolyl, tetrahydronaphthyl, dihydrobenzofuranyl, and tetrahydroquinolinyl.

Further preferred compounds of the instant invention are realized when in the above structural formula: R2 and R3 are hydrogen or methyl; X is -CH2- m is 1 ; r is 0-2; and

R4, R5 and R6 are hydrogen.

Still further preferred compounds of the instant invention are realized when in the above structural formula: A is phenyl, quinolinyl, or a 6-membered heterocyclic ring with

1 or 2 nitrogen atoms;

B is phenyl or quinolinyl;

Rl is NH2, hydroxy, halogen, cyano, trifluoromethyl, phenyl,

NR8COR9, NR8C02R8, C1-C6 alkyl optionally substituted by hydroxy; and r is 0 or 2.

Representative preferred antiobesity and antidiabetic compounds of the present invention include the following:

N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyllamino]ethy l]phenyl]- benzenesulfonamide

]sj_[4_[2-ff2-hydroxy-3-(4-hydroxyphenoxy)propyl]aminoIet hyl]phenyll-

4-iodobenzenesulfonamide

N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]ethy l]phenylJ-

2-naphthalenesulfonamide

N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]ethy l]phenylj-

4-(benzo-2, 1 ,3-thiadiazole)sulfonamide

N-[4-[2-[f2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]ethy l]phenylJ-

2-phenylethanesulfonamide

N-[4-[2-[[3-(4-fluorophenoxy)-2-hydroxypropylJamino]ethyl ]phenyl]-

4-benzenesulfonamide

N-[4-[2-[[3-[(2-amino-5-pyridinyl)oxy]-2-hydroxypropyl]am ino]ethyl]- phenyl]-2-naphthalenesulfonamide

N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]ethy l]phenyl]-

3-quinolinesulfonamide

N _. -[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]et hyl]phenyl]-

4-[(5-methoxycarbonyl)pentanoyl]amino]benzenesulfonamide

N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]ethy l]phenyl ]-

4-f(5-hydroxycarbonyl)pentanoyl]amino]benzenesulfonamide

N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]ethy l]phenyl]-

4-(hexylaminocarbonylamino)benzenesulfonamide

N-[4-[2-[(2-hydroxy-3-phenoxypropyl)amino]ethyl]phenyl]-4 - chlorobenzenesulfonamide

N-[4-f2-[f2-hydroxy-3-(3-cyanophenoxy)propyl]amino]ethyl]phe nyI]-3- quinolinesulfonamide

N-[4-[2-[[3-(4-amino-3-cyanophenoxy)-2-hydroxypropyl]amin o]ethyl]- pheny 1 ]-3 -quinolinesulf onamide

N-[4-[2-[[2-hydroxy-3-[(3-hydroxymethyl)phenoxy]propyljam ino]- ethy ljpheny 1] -3 -quinolinesu If onamide

N-[4-[2-[[2-hydroxy-3-(3-pyridyloxy)propyl]amino]ethyl]ph enyl]-3- quinolinesulfonamide

N-[4-[2-[[2-hydroxy-3-(3-pyridyloxy)propyl]amino]ethyl]ph enyl]-4- iodobenzenesulfonamide

N-[4-[2-[[3-[(2-amino-5-pyridinyl)oxy]-2-hydroxypropyl]am ino]ethyl]- phenyl]-4-isopropylbenzenesulfonamide.

The compounds of the instant invention all have at least one asymmetric center as noted by the asterisk in structural Formulae I and la. Additional asymmetric centers may be present on the molecule depending upon the nature of the various substituents on the molecule, in particular, R2 and R3. Each such asymmetric center will produce two optical isomers and it is intended that all such optical isomers, as separated, pure or partially purified optical isomers or racemic mixtures thereof, be included within the ambit of the instant invention. In the case of the asymmetric center represented by the asterisk in Formula I, it has been found that the compound in which the hydroxy substituent is above the plane of the structure, as seen in Formula la, is more active and thus more preferred over the compound in which the hydroxy substituent is below the plane of the structure.

Compounds of the general Formula I may be separated into diastereoisomeric pairs of enantiomers by, for example, fractional crystallization from a suitable solvent, for example methanol or ethyl acetate or a mixture thereof. The pair of enantiomers thus obtained may be separated into individual stereoisomers by conventional means, for example by the use of an optically active acid as a resolving agent.

Alternatively, any enantiomer of a compound of the general Formula I may be obtained by stereospecific synthesis using optically pure starting materials of known configuration.

The following stereospecific structure represents the preferred stereoisomers of the instant invention.

la

where the various substituents are as defined above.

The instant compounds can be isolated in the form of their pharmaceutically acceptable acid addition salts, such as the salts derived from using inorganic and organic acids. Examples of such acids are hydrochloric, nitric, sulfuric, phosphoric, formic, acetic, trifluoroacetic, propionic, maleic, succinic, malonic and the like. In addition, certain compounds containing an acidic function such as a carboxy or tetrazole, can be isolated in the form of their inorganic salt in which the counterion can be selected from sodium, potassium, lithium, calcium, magnesium and the like, as well as from organic bases. The compounds (I) of the present invention can be prepared from epoxide intermediates such as those of formula II and amine intermediates such as those of formula III. The preparation of these intermediates is described in the following schemes.

where n, m, r, A, Rl , R2, R3, R4, R5, R6, R7 and X are as defined above.

Compounds II can be conveniently prepared by a variety of methods familiar to those skilled in the art. One common route is illustrated in Scheme 1. Alcohol 1 is treated with base such as sodium hydride or potassium t-butoxide in a polar solvent such as anhydrous dimethylformamide. The resultant anion is alkylated with epoxide derivative 2, wherein "L" is a leaving group such as a sulfonate ester or a halide, for 0.5 to 24 hours at temperatures of 20-100°C to provide compound II. The epoxide derivative 2 is conveniently the commercially available, enantiomerically pure (2S) or (2/?)-glycidyI 3- nitrobenzene sulfonate or (2R) or (2S)-glycidyl 4-toluenesulfonate, thus both the (S) and (R) enantiomers of epoxide II are readily available.

,0

Many of the alcohols 1 are commercially available or readily prepared by methods described in the literature and known to those skilled in the art. Rl substituents on the alcohol 1 may need to be protected during the alkylation and subsequent procedures. A description of such protecting groups may be found in: Protective Groups in Organic Synthesis. 2nd Ed., T. W. Greene and P. G. M. Wuts, John Wiley and Sons, New York, 1991. A useful method for protecting the preferred alchohol 1 wherein A (Rl )n is 4-hydroxy- phenyl as its rerr-butyldimethylsilyl (TBS) derivative is illustrated in Scheme 2. Commercially available phenol 3 _. is treated with a silylating

agent such as tøt -butyldimethylsilyl chloride in the presence of a base such as imidazole in an aprotic solvent such as dimethylformamide. The benzyl group is then removed by catalytic hydrogenation to give the desired alcohol 5.

SCHEME 2

d catalyst

Compounds HI can be conveniently prepared by a variety of methods familiar to those skilled in the art. A convenient route for their preparation when R6 is hydrogen is illustrated in Scheme 3. Compound 6 is selectively protected as a suitable carbamate derivative 6a with, for example, di-te/J-butyl dicarbonate or carbobenzyloxy chloride. This compound is then treated with a sulfonyl halide, preferably the sulfonyl chloride 7, and a base such as pyridine in an anhydrous solvent such as dichloromethane or chloroform for 0.5 to 24 hours at temperatures of -20 to 50°C, preferably 0°C, to provide the sulfonamide 8. The protecting group is then removed with, for example, trifluoracetic acid in the case of Boc or catalytic hydrogenation in the case of Cbz, to give the desired amine 9.

SCHEME 3

9

Compounds III where R6 is not hydrogen may be conveniently prepared as illustrated in Scheme 4. Sulfonamide _{_ prepared as described above, is alkylated with an appropriate alkylating agent 10 in the presence of base to provide sulfonamide JJ _. . Removal of the protecting group as above gives the desired compound HI.

SCHEME 4

R ^< R ⁶ -Y

1 I 0 u

GNH-C (X) m >-NS0 ₂ (CH ₂ ) _r -R ⁷ I

R° D5 H base

III

The sulfonyl chlorides 7, many of which are commercially available, can also be readily prepared by a number of methods familiar to those skilled in the art. One suitable method involves the addition of an organolithium reagent or a Grignard reagent to sulfuryl chloride following the procedure of S. N. Bhattacharya, et. ah, J. Chem. Soc. (C), 1265-1267 (1968). Another convenient method involves the treatment of a thiol with sulfuryl chloride and a metal nitrate according to the procedure of Y. J. Park, et. al., Chemistry Letters, 1483-1486 (1992). Sulfonic acids are also conveniently converted to the corresponding sulfonyl chloride by treatment with PCI5, PCI3 or SOCI2 (J. March, Advanced Organic Chemistry. 4th Ed., John Wiley and Sons, New York: 1992, pl297 and references cited therein). Alternatively, aromatic compounds may be treated with chlorosulfonic acid according to the procedure of Albert, et. al.. J. Het. Chem. 15. 529 (1978), to provide the sulfonyl chlorides.

The diamines 6 are commercially available or readily prepared by methods described in the literature or known to those skilled in the art. Compound 6 where R2 or R3 is methyl can be prepared from the corresponding amino acid following the method of J. D. Bloom, et. al, J. Med. Chem., 35, 3081-3084 (1992). As illustrated in Scheme 5 for R3 = methyl, the appropriate (R) amino acid 12 is esterified, conveniently by treatment with methanolic hydrochloric acid, and then treated with άi-tert-h ty\ dicarbonate to give compound 13. The ester group is reduced with a hydride source such as lithium borohydride and the resultant alcohol is converted to a leaving group such as a mesylate. Removal of the Boc protecting groups gives diamine ____. This compound is subjected to catalytic hydrogenation in the presence of base such as sodium acetate to give the desired oc-methyl amine 15. The other enantiomer is available through an analogous sequence starting with the corresponding (S) amino acid.

SCHEME 5

Diamines 6 or sulfonamide amines 9 where X is -CH2O- and m is 1 are also readily prepared by methods described in the literature or known to those skilled in the art. For example, as shown in Scheme 6, the sodium salt of 4-nitrophenol 16 is alkylated with 1 - bromo-2-chloroethane, conveninetly in refluxing 2-butanone with a base such as potassium carbonate, to give chloro derivative JJ _. . The chloride is converted to the corresponding amine by treatment with lithium azide followed by reduction with, for example, triphenylphosphine in aqueous tetrahydrofuran. Protection of the resultant amine, conveniently as its t-butyl carbamate by treatment with di-tert-butvldicarbonate, gives

derivative J_8. The nitro group is then reduced, for example, by catalytic hydrogenation to provide amine J_9. Acylation of intermediate 19 with sulfonyl chloride 7, followed by deprotection with acid such as trifluoroacetic acid gives the desired intermediate 20.

SCHEME 6

1£

H ₂ , Pd/C

BOCNH

ιa

2Q

Alternatively, diamine 6 where X is -CH2O- and m is 1 is available from intermediate \ 9_ by treatment with trifluoroacetic acid. This diamine may then be modified as illustrated in Scheme 3.

Diamines 6 and sulfonamide amines 9 where X is -CH2CH2- and m is 1 are also readily prepared by methods described in the literature or known to those skilled in the art. For example, as shown in Scheme 7, bromo derivative 21 is treated with sodium cyanide to provide nitrile 22. The nitro group is selectively reduced by treatment with hydrogen and catalytic palladium to provide amine 23. Amine 23 is acylated with sulfonyl chloride 7 to give the corresponding sulfonamide 24. Reduction of compound 24 with cobalt chloride and sodium borohydride provides the desired amine 25.

SCHEME 7

H _2> Pd/C R ⁷ (CH ₂ ) _r S0 ₂ CI (Z)

MeOH _N H ₂ pyridine, CH ₂ CI ₂

23

Alternatively, diamine 6 where X is -CH2CH2- and m is 1 is available from intermediate 23 _. by reduction of the nitrile group with, for example, cobalt chloride and sodium borohydride. This diamine may then be modified as illustrated in Scheme 3.

Intermediates II and III are coupled by heating them neat or as a solution in a polar solvent such as methanol, acetonitrile, tetrahydrofuran, dimethylsulfoxide or /V-methyl pyrrohdinone for 1 to 24 hours at temperatures of 30 to 150°C to provide compounds I as shown in Scheme 8. The reaction is conveniently conducted in refluxing methanol. Alternatively, a salt of amine III, such as the trifluoroacetate or hydrochloride salt, may be used. In these cases, a

base such as sodium bicarbonate or diisopropylethylamine is added to the reaction mixture. The product is purified from unwanted side products by recrystallization, trituration, preparative thin layer chromatography, flash chromatography on silica gel as described by W. C. Still, et. ah, J. Org. Chem. 43, 2923 (1978), medium pressure liquid chromatography, or HPLC. Compounds which are purified by HPLC may be isolated as the corresponding salt. Purification of intermediates is achieved in the same manner.

SCHEME 8

In some cases, the coupling product I from the reaction described in Scheme 8 may be further modified, for example, by the removal of protecting groups or the manipulation of substituents on, in particular, Rl and R7. These manipulations may include reduction, oxidation, alkylation, acylation, and hydrolysis reactions which are commonly known to those skilled in the art. One such example is illustrated in Scheme 9. Compound 26, which is prepared as outlined in the Scheme 8 from the corresponding epoxide, is subjected to catalytic

hydrogenation in a polar solvent such as 1 : 1 acetic acid/methanol to provide compound 27. Other examples of substituents on compound I which may be reduced to the corresponding amine by catalytic hydrogenation and methods commonly known to those skilled in the art include nitro groups, nitriles, and azides.

SCHEME 9

21

Scheme 10 illustrates an example of another such modification of the coupling product I. Acetamido derivative 28, which is prepared as outlined in the Scheme 8 from the corresponding epoxide, is subjected to hydrolysis in a protic solvent such as methanol/water with added acid or base such as hydrochloric acid or sodium hydroxide to provide the corresponding aniline derivative 29.

SCHEME 10

(Y = CH, N)

HCI or NaOH MeOH-H ₂ 0

An alternate method for the synthesis of compound I is illustrated in Scheme 1 1. Epoxide II is coupled to amine 6 as described above for coupling intermediates II and IH (Scheme 8) to give aniline derivative 31 a. The secondary amine is selectively protected, for example, as a carbamate by treatment with di-fe/7-butyldicarbonate to provide carbamate 32. Alternatively, nitro amine 30 is used in the coupling reaction to provide 31b. Following protection as described above, the nitro group is reduced, for example, by catalytic hydrogenation, to provide intermediate 32. Treatment with a sulfonyl chloride in the presence of a base such as pyridine followed by removal of the protecting group with, in the case of a ter/-butylcarbamate, acid such as trifluoroacetic acid or methanolic hydrogen chloride, provides the sulfonamide I.

SCHEME 1 1

H (Z = NH ₂ ) 3D. (Z = N0 ₂ )

1) R ⁷ (CH ₂ ) _r -S0 ₂ CI, base

2) TFA or HCI/MeOH

In some cases, sulfonamide I from the reaction sequence illustrated in Scheme 11 may be further modified, for example, by the removal of protecting groups or the manipulation of substituents on, in particular, Rl and R7, as described above. In addition, manipulation of substituents on any of the intermediates in the reaction sequence illustrated in Scheme 1 1 may occur. An example of this is illustrated in

Scheme 12. N-Boc 4-nitrobenzenesulfonamide 33, which is prepared from intermediate 32 and 4-nitrobenzenesulfonyl chloride, is subjected to catalytic hydrogenation and the resultant aniline is acylated with, for example, an acid chloride in the presence of base to give N-Boc intermediate 34- Deprotection with acid such as trifluoroacetic acid or methanolic hydrogen chloride provides the desired sulfonamide 35.

SCHEME 12

33

1) H ₂ , catalytic Pd/C

2) R ⁸ COCI, pyridine

TFA or HCI/MeOH

As previously indicated, the compounds of the present invention have valuable pharmacological properties.

The present invention also provides a compound of the general Formula I or a pharmaceutically acceptable salt thereof for use as an active therapeutic substance.

In one aspect, the present invention provides a compound of the general Formula I or a pharmaceutically acceptable ester thereof: or a pharmaceutically acceptable salt thereof for use in the treatment of obesity in human or non-human animals.

The present invention further provides a compound of the general Formula I, or a pharmaceutically acceptable ester thereof; or pharmaceutically acceptable salt thereof, for use in the treatment of hyperglycemia (diabetes) in human or non-human animals.

The disease diabetes mellitus is characterized by metabolic defects in production and utilization of glucose which result in the failure to maintain appropriate blood sugar levels. The result of these defects is elevated blood glucose or hyperglycemia. Research on the treatment of diabetes has centered on attempts to normalize fasting and postprandial blood glucose levels. Treatments have included parenteral administration of exogenous insulin, oral administration of drugs and dietary therapies.

Two major forms of diabetes mellitus are now recognized. Type I diabetes, or insulin-dependent diabetes, is the result of an absolute deficiency of insulin, the hormone which regulates glucose utilization. Type II diabetes, or insulin-independent diabetes, often occurs in the face of normal, or even elevated levels of insulin and appears to be the result of the inability of tissues to respond appropriately to insulin. Most of the Type II diabetics are also obese.

In addition the compounds of the present invention lower triglyceride levels and cholesterol levels and raise high density lipoprotein levels and are therefore of use in combatting medical conditions wherein such lowering (and raising) is thought to be beneficial. Thus they may be used in the treatment of hyper- triglyceridaemia, hypercholesterolaemia and conditions of low HDL (high density lipoprotein) levels in addition to the treatment of

atherosclerotic disease such as of coronary, cerebrovascular and peripheral arteries, cardiovascular disease and related conditions.

Accordingly, in another aspect the present invention provides a method of lowering triglyceride and/or cholesterol levels and/or increasing high density lipoprotein levels which comprises administering, to an animal in need thereof, a therapeutically effective amount of a compound of the formula (I) or pharmaceutically acceptable salt thereof. In a further aspect the present invention provides a method of treating atherosclerosis which comprises administering, to an animal in need thereof; a therapeutically effective amount of a compound of the formula (I) or pharmaceutically acceptable salt thereof. The compositions are formulated and administered in the same general manner as detailed below for treating diabetes and obesity. They may also contain other active ingredients known for use in the treatment of atherosclerosis and related conditions, for example fibrates such as clofibrate, bezafibrate and ge fibrozil; inhibitors of cholesterol biosynthesis such as HMG-CoA reductase inhibitors for example lovastatin, simvastatin and pravastatin; inhibitors of cholesterol absorption for example beta-sitosterol and (acyl CoAxholesterol acyltransferase) inhibitors for example melinamide; anion exchange resins for example cholestyramine, colestipol or a dialkylaminoalkyl derivatives of a cross-linded dextran; nicotinyl alcohol, nicotinic acid or a salt thereof; vitamin E; and thyromimetics.

The compounds of the instant invention also have the effect of reducing intestinal motility and thus find utility as aiding in the treatment of various gastrointestinal disorders such as irritable bowel syndrome. It has been proposed that the motility of non-sphincteric smooth muscle contraction is mediated by activity at β3 adrenoreceptors. The availability of a β3 specific agonist, with little activity at βl and β2 receptors will assist in the pharmacologic control of intestinal motility without concurrent cardiovascular effects. The instant compounds are administered generally as described below with dosages similar to those used for the treatment of diabetes and obesity.

It has also been found unexpectedly that the compounds which act as agonists at β3 adrenoreceptors may be useful in the treatment of gastrointestinal disorders, especially peptic ulcerations, esophagitis, gastritis and duodenitis, (including that induced by H. pylori), intestinal ulcerations (including inflammatory bowel disease, ulcerative colitis, Crohn's disease and proctitis) and gastrointestinal ulcerations.

In addition, β3 receptors have been indicated to have an effect on the inhibition of the release of neuropeptides in certain sensory fibers in the lung. As sensory nerves may play an important role in the neurogenic inflammation of airways, including cough, the instant specific β3 agonists may be useful in the treatment of neurogenetic inflammation , such as asthma, with minimal effects on the cardio- pulmonary system. β3 adrenoreceptors are also able to produce selective antidepressant effects by stimulating the β3 receptors in the brain and thus an additional contemplated utility of the compounds of this invention are as antidepressant agents.

The active compounds of the present invention may be orally administered as a pharmaceutical composition, for example, with an inert diluent, or with an assimilable edible carrier, or they may be enclosed in hard or soft shell capsules, or they may be compressed into tablets, or they may be incorporated directly with the food of the diet. For oral therapeutic administration, which includes sublingual adminastration, these active compounds may be incorporated with excipients and used in the form of tablets, pills, capsules, ampules, sachets, elixirs, suspensions, syrups, and the like. Such compositions and preparations should contain at least 0.1 percent of active compound. The percentage of active compound in these compositions may, of course, be varied and may conveniently be between about 2 percent to about 60 percent of the weight of the unit. The amount of active compound in such therapeutically useful compositions is such that an effective dosage will be obtained. The active compounds can also be adminastered intranasally as, for example, liquid drops or spray.

The effective dosage of active ingredient employed may vary depending on the particular compound employed, the mode of administration, the condition being treated and the severity of the condition being treated.

When treating diabetes mellitus and/or hyperglycemia generally satisfactory results are obtained when the compounds of the present invention are administered at a daily dosage of from about 0.1 milligram to about 1 milligram per kilogram of animal body weight, preferably given in divided doses two to six times a day, or in sustained release form. For most large mammals, the total daily dosage is from about 3.5 milligrams to about 140 milligrams, preferably from about 3.5 milligrams to about 5 milligrams. In the case of a 70 kg adult human, the total daily dose will generally be from about 7 milligrams to about 70 milligrams. This dosage regimen may be adjusted to provide the optimal therapeutic response.

When treating obesity, in conjunction with diabetes and/or hyperglycemia, or alone, generally satisfactory results are obtained when the compounds of the present invention are administered at a daily dosage of from 1 milligram to about 10 milligrams per kilogram of animal body weight, preferably given in divided doses two to six times a day, or in sustained release form. For most large mammals, the total daily dosage is from about 35 milligrams to about 1 ,400 milligrams, preferably from about 35 milligrams to about 50 milligrams. In the case of a 70 kg adult human, the total daily dose will generally be from about 70 milligrams to about 700 milligrams. This dosage regimen may be adjusted to provide the optimal therapeutic response.

The tablets, pills, capsules, and the like may also contain a binder such as gum tragacanth, acacia, corn starch or gelatin; excipients such as dicalcium phosphate; a disintegrating agent such as com starch, potato starch, alginic acid; a lubricant such as magnesium stearate; and a sweetening agent such as sucrose, lactose or saccharin. When a dosage unit form is a capsule, it may contain, in addition to materials of the above type, a liquid carrier such as a fatty oil.

Various other materials may be present as coatings or to modify the physical form of the dosage unit. For instance, tablets may be coated with shellac, sugar or both. A syrup or elixir may contain, in addition to the active ingredient, sucrose as a sweetening agent, methyl and propylparabens as preservatives, a dye and a flavoring such as cherry or orange flavor.

These active compounds may also be administered parenterally. Solutions or suspensions of these active compounds can be prepared in water suitably mixed with a surfactant such as hydroxy - propylcellulose. Dispersions can also be prepared in glycerol, liquid polyethylene glycols and mixtures thereof in oils. Under ordinary conditions of storage and use, these preparations contain a preservative to prevent the growth of microorganisms.

The pharmaceutical forms suitable for injectable use include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersions. In all cases, the form must be sterile and must be fluid to the extent that easy syringability exists. It must be stable under the conditions of manufacture and storage and must be preserved against the contaminating action of microorganisms such as bacteria and fungi. The carrier can be a solvent or dispersion medium containing, for example, water, ethanol, polyol (e.g. glycerol, propylene glycol and liquid polyethylene glycol), suitable mixtures thereof, and vegetable oils.

The following examples are provided so that the invention might be more fully understood. They should not be construed as limiting the invention in any way.

EXAMPLE 1

(S -2-r (4-Phenylmethoxy phenoxylmethylloxirane

A solution of 1.54 g (7.72 mmol) of 4-benzyloxyphenol in 10 mL of dimethylformamide (DMF) was added dropwise via cannula to a mixture of 310 mg (7.72 mmol) of sodium hydride (60% dispersion in mineral oil). After the mixture was allowed to stir for 1 h, a solution of 2.00 g (7.72 mmol) of (2S)-glycidyl 3-nitrobenzene sulfonate in 10 mL of DMF was added via cannula. The reaction mixture was allowed to stir at room temperature for 4.5 h. It was diluted with ethyl acetate, washed with three portions of water, dried over magnesium sulfate, and concentrated. Purification by flash chromatography (silica gel, 20% ethyl acetate/hexane) gave 1.84 g (93%) of the title compound: l H NMR (200 MHz, CDCI3) δ 7.41 -7.28 (m, 5H), 6.90-6.80 (sym m, 4H), 4.99 (s, 2H), 4.14 (dd, IH, J = 3.2, 1 1 Hz), 3.89 (dd, IH, J = 5.6, 1 1 Hz), 3.29 (m, IH), 2.86 (t, I H, J = 5.1 Hz), 2.71 (dd, IH, J = 2.6, 5.1 Hz); El MS ml 2 256 (M), 165, 91.

EXAMPLE 2

(S)-2-[[4-[[(l ,l-Dimethylethyl)dimethylsilyl]oxy]phenoxy]methylJ- oxirane

A solution of 10.0 g (50.0 mmol) of 4-benzyloxyphenol, 9.04 g (60.0 mmol) of r -butyldimethylsilyl chloride, and 4.42 g (65.0 mmol) of imidazole in dimethylforamide (DMF) was allowed to stir at ambient temperature overnight. The mixture was then diluted with ethyl acetate, washed sequentially with water, 1 M aqueous sodium bisulfate solution, 1 M aqueous sodium hydroxide solution, and brine, dried over magnesium sulfate, and concentrated to give a white solid. The unpurified compound was dissolved in 40 mL of ethyl acetate and allowed to stir over 20% palladium hydroxide on carbon under an atmosphere of hydrogen overnight. The reaction mixture was then filtered through a pad of Celite and concentrated. The resultant phenol

was dissolved in 40 mL of DMF and added dropwise over a 30-min period via cannula to a mixture of 2.60 g (65.0 mmol) of sodium hydride (60% dispersion in mineral oil) at 0°C. A 10-mL portion of DMF was added. After the mixture was allowed to stir at 0°C for 30 min, a solution of 14.3 g (55.0 mmol) of (2S _. )-glycidyl 3-nitrobenzene sulfonate in 40 mL of DMF was added dropwise over a 20-min period. After the reaction was judged to be complete by TLC analysis, it was quenched with water, diluted with ethyl acetate, washed sequentially with water, 1 M aqueous sodium hydroxide solution, and brine, dried over magnesium sulfate, and concentrated. Purification by flash chromatography (silica gel, 10% ethyl acetate/hexane) gave 5.04 g (36% overall yield) of the title compound: l H NMR (400 MHz, CD3OD) δ 6.82 (d, 2H, J = 9.1 Hz), 6.74 (d, 2H, J = 9.1 Hz), 4.22 (dd, IH, J = 2.6, 1 1.2 Hz), 3.79 (dd, IH, J = 6.2, 1 1.2 Hz), 3.30 (m, I H), 2.84 (t, IH, J = 4.6 Hz), 2.71 (dd, IH, J = 2.7, 5.0 Hz), 0.97 (s, 9H), 0.15 (s, 6H).

EXAMPLE 3 CbzNH.

NH

2-(4-Aminophenyl ethylcarbamic acid phenylmethyl ester

A solution of 5.00 g (36.7 mmol) of 2-(4-aminophenyl)- ethylamine in 100 mL of chloroform was cooled to 0°C and 3.72 g

(5.20 mL, 36.8 mmol) of triethylamine was added. A solution of 6.26 g (5.2 mL, 36.8 mmol) of benzyl chloroformate in 40 mL of chloroform was then added dropwise over a 30-min period. The reaction was allowed to stir at 0°C for 2 h. It was diluted with 100 mL of chloroform, washed with 100-mL portions of water and brine, dried over sodium sulfate and concentrated. The residue was dissolved in 50% ethyl acetate/hexane and stirred with 30 g of silica gel, filtered, and concentrated. Further purification by recrystallization from ethyl acetate/hexanes gave 4.82 g (49%) of the title compound as a white solid: lH NMR (400 MHz, CDCI3) 7.33 (s, 5H), 6.94 (d, 2H, J = 8.2

Hz), 6.60 (d, 2H, J = 8.2 Hz), 5.07 (s, 2H), 4.84 (broad s, IH), 3.55 (broad s, 2H), 3.37 (m, 2H), 2.67 (t, 2H, J = 6.9 Hz). FAB MS mlz 271 (M + 1 ).

EXAMPLE 4

BocN

2-(4-Aminophenyl)ethylcarbamic acid l J -dimethylethyl ester

A solution of 817 mg (6.00 mmol) of 2-(4-aminophenyl)- ethylamine in 20 mL of tetrahydrofuran was treated with 1310 mg (6.00 mmol) of di-tert-butyl dicarbonate. After the reaction mixture was stirred at room temperature for 0.5 h, it was concentrated. Trituration from a solution of 5 mL of ether and 20 mL of hexane gave 1.04 g (73%) of the title compound as a pale yellow solid: lH NMR (400 MHz, CDC13) 6.94 (d, 2H, j = 8.2 Hz), 6.59 (d, 2H, J = 8.2 Hz), 4.51 (broad s, IH), 3.58 (broad s, 2H), 3.27 (m, 2H), 2.63 (t, 2H, J = 7.0 Hz), 1.38 (s, 9H). FAB MS mlz 237 (M + 1).

EXAMPLE 5

CbzN

N-[4-f2-[(phenylmethoxycarbonyl)amino]ethyl]phenyl]benzen esulfon- amide

A solution of 868 mg (3.22 mmol) of Cbz amine from Example 3 in 15 mL of dichloromethane was cooled to 0°C and treated with 0.286 mL (3.54 mmol) of pyridine followed by 569 mg (0.41 mL, 3.22 mmol) of benzenesulfonyl chloride. The reaction mixture was stirred at room temperature for 2 h and then partitioned between chloroform and water. The organic phase was washed sequentially with 5% aqueous hydrochloric acid and saturated aqueous sodium

bicarbonate, dried over magnesium sulfate, and concentrated. Purification by recrystallization from ethyl acetate/hexane gave 630 mg (48%) of the title compound as a white solid: 1 H NMR (400 MHz, . CDC13) 7.72 (d, 2H, J = 7.2 Hz), 7.48 (m, IH), 7.39 (m, 2H), 7.33 (m, 5H), 7.02 (d, 2H, J = 8.3 Hz), 6.95 (d, 2H, J = 8.3 Hz), 6.55 (s, IH), 5.06 (s, 2H), 4.68 (broad s, I H), 3.37 (m, 2H), 2.72 (t, 2H, J = 6.9 Hz). FAB MS /z 41 1 (M + 1 ).

EXAMPLE 6

N-[4-(2-aminoethyl phenyl1benzenesulfonamide

A solution of 600 mg (1.46 mmol) of Cbz amine from Example 5 in 18 mL of methanol was stirred over 20% palladium hydroxide on carbon under an atmosphere of hydrogen for 2.5 h. The reaction mixture was filtered through a Celite pad and concentrated to give 360 mg (89%) of a white solid: lH NMR (400 MHz, CD3OD) δ

7.73 (d, 2H, J = 7.1 Hz), 7.52 (t, IH, J = 7.4 Hz), 7.44 (t, 2H, J = 7.5 Hz), 7.04 (d, 2H, J = 8.7 Hz), 6.99 (d, 2H, J = 8.6 Hz), 2.82 (t, 2H, J = 7.3 Hz), 2.66 (t, 2H, J = 7.3 Hz).

(S)-N-[4-[2-[[2-hydroxy-3-[(4-phenylmethoxy)phenoxy]propy l]amino]- ethyllphenyllbenzenesulfonamide

A solution of 406 mg (1.47 mmol) of amine from Example 6 in 8 mL of anhydrous methanol was treated with 280 mg (1.10 mmol)

of epoxide from Example 1. The solution was heated at reflux under nitrogen overnight, then cooled to room temperature and concentrated. Purification by flash chromatography (silica gel, 5:4: 1 ethyl acetate .hexane: 10% methanolic ammonium hydroxide) gave 282 mg (48%) of the title compound: NMR (400 MHz, CD3OD) δ 7.71 (d, 2H), 7.52 (m, IH), 7.1 -7.4 (7H), 7.06 (d, 2H), 7.00 (d, 2H), 6.75 (d, 2H), 6.70 (d, 2H), 5.02 (s, 2H), 3.99 (m, IH), 3.82 (d, 2H), 2.6-2.9 (m, 6H).

EXAMPLE 8

(S _. )-N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]a phenyllbenzenesulfonamide

A solution of 282 mg (0.529 mmol) of benzyl ether from Example 7 in 5 mL of methanol and 5 mL of tetrahydrofuran was treated with 100 mg of 20% palladium hydroxide on carbon under an atmosphere of hydrogen for 2 h. It was then filtered and concentrated. Purification by flash chromatography (silica gel, 5:4:2 ethyl acetate:hexane:10% methanolic ammonium hydroxide) gave 141 mg (60%) of the title compound as a foam: lH NMR (400 MHz, CD3OD) 7.71 (d, 2H, J = 7.1 Hz), 7.52 (m, IH), 7.43 (m, 2H), 7.07 (d, 2H, J = 8.5 Hz), 6.99 (d, 2H, J = 8.5 Hz), 6.75 (d, 2H, J = 9.1), 6.68 (d, 2H, J = 9.1 Hz), 3.98 (m, IH), 3.82 (d, 2H, J = 5.4 Hz), 2.6-2.9 (m, 6H). FAB MS mlz 443 (M + 1).

EXAMPLE 9

N-f4-[2-[l(l ,l -dimethylethoxy)carbonyl]amino]ethyl]phenyl]-4- iodobenzenesulfonamide

In a manner analogous to that of Example 5, the title compound was prepared from the Boc amine in Example 2 and 4- iodobenzenesulfonyl chloride: lH NMR (400 MHz, CD3OD) δ 7.86 (d, 2H), 7.46 (d, 2H), 7.07 (d, 2H), 6.99 (d, 2H), 3.27 (t, 2H), 2.76 (t, 2H), 1.38 (s, 9H).

EXAMPLE 10

N-[4-(2-aminoethyl)phenyll-4-iodobenzenesulfonamide

A solution of 1.80 g of Boc amine from Example 9 in 1 : 1 trifluoroacetic acid:dichloromethane was allowed to stand at room temperature for 15 min at which time TLC analysis indicated the reaction was complete. The solution was then concentrated. Purification by flash chromatography (silica gel, 15% of 10: 1 methanol oncentrated ammonium hydroxide in dichloromethane) gave the title compound as a crystalline solid: lH NMR (200 MHz, CD3OD) δ 7.80 (d, 2H), 7.46 (d, 2H), 7.06 (d, 2H), 6.98 (d, 2H), 2.81 (t, 2H), 2.65 (t, 2H).

EXAMPLE 1 1

(S)-N-[4-[2-[[2-hydroxy-3-f[4-[[(l ,l -dimethylethyl)dimethylsilyl]oxy|- phenoxylpropyllaminolethyllphenyll-4-iodo-benzenesulfonamide In a manner analogous to that of Example 7, the title compound was prepared from the epoxide from Example 2 and the amine from Example 10: l H NMR (400MHz, CD3OD) δ 7.82 (d, 2H, J = 8.6 Hz), 7.43 (d, 2H, 8.6 Hz), 7.10 (d, 2H, J = 8.5 Hz), 6.79 (d, 2H), 6.73 (d, 2H), 4.01 (m, IH), 3.87 (d, 2H), 3.91 -2.69 (m, 6H), 0.96 (s, 9H), 0.15 (s, 6H).

EXAMPLE 12

(S)-N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino] ethyll- phenyll-4-iodobenzenesulfonamide

A 1 2-mg (0.266 mmol) sample of silyl ether from Example 1 1 was treated with 3% methanolic hydrogen chloride (prepared by adding 1 mL of acetyl chloride to 19 mL of methanol at 0°C). After the solution was allowed to stir at room temperature for lh, it was concentrated. Purification by flash chromatography (silica gel, 10% of 10: 1 methanol oncentrated ammonium hydroxide in dichloromethane) gave 106 mg (70%) of the title compound: lH NMR (400MHz, CD3OD) δ 7.82 (d, 2H, J = 8.6 Hz), 7.43 (d, 2H, 8.6 Hz),

7.10 (d, 2H, J = 8.5 Hz), 6.99 (d, 2H, J = 8.5 Hz), 6.74 (d, 2H, J = 9.0 Hz), 6.68 (d, 2H, J = 9.0 Hz), 4.00 (m, I H), 3.83 (d, 2H, J = 5.5 Hz), 3.34-2.67 (m, 6H); FAB MS mlz 569 (M + 1 ), 309, 154.

EXAMPLE 13

N _. -[4-[2-f(phenylmethoxycarbonyl)amino]ethyl]phenyl]-2-n aphthalene- sulfonamide

In a manner analogous to that of Example 5, the title compound was prepared from the Cbz amine from Example 3 and 2- naphthalenesulfonyl chloride: l H NMR (400 MHz, CDCI3) δ 8.32 (s, IH), 7.85 (m, 3H), 7.71 (dd, IH, J = 1.8, 8.7 Hz), 7.61 -7.52 (m, 2H), 7.34-7.28 (m, 5H), 6.99 (s, 4H), 6.77 (br s, IH), 5.04 (s, 2H), 4.65 (br s, IH), 3.33 (br q, 2H, J = 5.9 Hz), 2.68 (t, 2H, J = 7.0 Hz); FAB MS ml z 461 (M + 1), 270.

(S)-N-[4-[2-[f2-hydroxy-3-[(4-phenylmethoxy)phenoxy]propy I]aminoJ- ethyllphenyll-2-naphthalenesulfonamide

The Cbz amine from Example 13 was deprotected as described in Example 6. In a manner analogous to that of Example 7, the title compound was prepared from the resultant amine and the epoxide from Example 1 : lH NMR (400 MHz, CD3OD) δ 8.27 (s, IH), 7.93-7.87 (m, 3H), 7.71 (dd, IH, J = 1.9, 8.7 Hz), 7.62-7.54 (m, 2H),

7.39 (d, 2H, J = 7.2 Hz), 7.34 (t, 2H, J = 7.3 Hz), 7.27 (t, IH, J = 7.1 Hz), 7.04 (d, 2H, J = 9.0 Hz), 7.01 (d, 2H, J = 9.0 Hz), 6.88 (d, 2H, J - 9.1 Hz), 6.79 (d, 2H, J = 9.1 Hz), 4.99 (s, 2H), 3.96 (m, IH), 3.82 (d, 2H, J = 5.3 Hz), 2.80-2.63 (m, 6H); FAB MS mlz 583 (M + 1).

EXAMPLE 15

(S)-N-[4-12-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino] ethyl]- phenyl1-2-naphthalenesulfonamide

In a manner analogous to that of Example 8, the title compound was prepared from the benzyl ether from Example 14: lH NMR (400 MHz, CD3OD) δ 8.28 (s, IH), 7.95-7.89 (m, 3H), 7.72 (dd,

IH, J = 1.9, 8.7 Hz), 7.62-7.57 (m, 2H), 7.07-7.01 (m, 4H), 6.73 (d, 2H, J = 9.0 Hz), 6.67 (d, 2H, J = 9.0 Hz), 3.97 (m, IH), 3.81 (d, 2H, J = 5.2 Hz), 2.85-2.68 (m, 6H); FAB MS mlz 493 (M + 1).

EXAMPLE 16

N-[4-[2-[[(l,l-dimethylethoxy)carbonyl]amino]ethyl]phenyl ]-β- styrenesulfonamide

In a manner analogous to that of Example 5, the title compound was prepared from the Boc amine from Example 4 and β- styrenesulfonyl chloride: l H NMR (400 MHz, CDCI3) δ 7.47 (d, IH, J = 15.4 Hz), 7.42-7.33 (m, 5H), 7.1 1 (s, 4H), 6.77 (d, IH, J = 15.4 Hz),

6.56 (br s, IH), 4.48 (br s, I H), 4.10 (br m, 2H), 2.72 (t, 2H, J = 7.1 Hz), 1.39 (s, 9H).

EXAMPLE 17

N-[4-f 2-[[( 1 , 1 -dimethylethoxy)carbonyl Jamino )ethyl]phenyl]-2- phenylethanesulfonamide

A solution of 204 mg (0.507 mmol) of Boc amine from Example 16 in methanol was stirred over 20% palladium hydroxide under an atmosphere of hydrogen overnight. The reaction mixture was then filtered and concentrated. Purification by flash chromatography (silica gel, 30% ethyl acetate/hexane) gave 168 mg (82%) of the title compound as a white solid: lH NMR (200 MHz, CDCI3) δ 7.39-7.21 (m, 3H), 7.15-7.06 (m, 4H), 6.96 (d, 2H, J = 8.1 Hz), 6.25 (s, IH), 4.49 (br s, IH), 3.35-3.24 (m, 4H), 3.18-3.05 (m, 2H), 2.72 (t, 2H, J = 7.1 Hz), 1.40 (s, 9H).

EXAMPLE 18

N-r4-(2-aminoethyl)phenyl1-2-phenylethanesulfonamide In a manner analogous to that of Example 10, the title compound was prepared from the Boc amine from Example 17: l H NMR (400 MHz, CD3OD) δ 7.25-7.12 (m, 7H), 7.1 1 (d, 2H, J = 6.8 Hz), 3.26 (m, 2H), 3.03 (m, 2H), 2.86 (t, 2H, J = 7.4 Hz), 2.72 (t, 2H, J = 7.4 Hz).

EX AMPLE 19

(S)-N-[4-[2-[[2-hydroxy-3-[(4-phenylmeώoxy)phenoxy]propy llam ethyllphenvπ-2-phenylethanesulfonamide

In a manner analogous to that of Example 7, the title compound was prepared from the amine from Example 18 and the epoxide from Example 1 : lH NMR (400 MHz, CD3OD) δ 7.40-7.09 (m, 14H), 6.88 (d, 2H, J = 9.2 Hz), 6.81 (d, 2H, J = 9.2 Hz), 4.00 (m, IH), 3.85 (d, 2H, J = 5.3 Hz), 3.25 (m, IH), 3.02 (m, IH), 2.91-2.78 (m, 5H), 2.72 (dd, IH, J = 8.1, 12.2 Hz); FAB MS mlz 561 (M + 1 ).

EXAMPLE 20

(S)-N-[4-[2-[f2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino] ethyl]- phenyll-2-phenylethanesulfonamide

In a manner analogous to that of Example 8, the title compound was prepared from the benzyl ether from Example 19: lH NMR (400 MHz, CD3OD) δ 7.25-7.15 (m, 7H), 7.1 1 (d, 2H, J = 7.0 Hz), 6.75 (d, 2H, J = 9.1 Hz), 6.68 (d, 2H, J = 9.1 Hz), 4.05 (m, IH), 3.89-3.83 (overlapping dd, 2H), 3.26 (m, IH), 3.05-2.95 (m, 4H), 2.88- 2.82 (m, 3H); FAB MS mlz 471 (M + 1 ).

EX AMPLE 21

CbzNH

N-[4-[2-[(phenylmethoxycarbonyl)aminoJethyl ]phenyll-8-quinoline- sulfonamide

In a manner analogous to that of Example 5, the title compound was prepared from the Cbz amine from Example 3 and 8- quinolinesulfonyl chloride: lH NMR (400 MHz, d6-DMSO) 9.94 (s, IH), 9J2 (m, IH), 8.49 (dd, IH), 8.31 (dd, IH), 8.24 (dd, IH), 7.70 (m, 2H), 7.2-7.4 (m, 4H), 6.94 (d, 2H), 6.88 (d, 2H), 4.94 (s, 2H), 3.04 (m, 2H), 2.48 (t, 2H). FAB MS mlz 462 (M + 1 ).

EXAMPLE 22

(S)-N-[4-[2-[[2-hydroxy-3-[(4-phenylmethoxy)phenoxy]pro ethyllphenyπ-8-quinolinesulfonamide

The Cbz amine from Example 21 was deprotected as described in Example 6. In a manner analogous to that of Example 7, the title compound was prepared from the resultant amine and the epoxide from Example 1 : lH NMR (400 MHz, CD3OD) 9J2 ( , IH), 8.49 (d, IH), 8.31 (dd, IH), 8.24 (dd, IH), 7.3-7.5 (m, 7H), 7.07 (d, 2H, J = 8.5 Hz), 6.99 (d, 2H, J = 8.5 Hz), 6.75 (d, 2H, J = 9.1 ), 6.68 (d, 2H, J = 9.1 Hz), 5.04 (s, 2H), 3.98 (m, IH), 3.82 (d, 2H, J = 5.4 Hz), 2.5-2.9 (m, 6H). FAB MS mlz 584 (M + 1).

EXAMPLE 23

(S)-N-[4-[2-[f2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino] ethyI]- phenyll-8-quinolinesulfonamide

In a manner analogous to that of Example 8, the title compound was prepared from the benzyl ether from Example 22: 1 H NMR (400 MHz, CD3OD) 9.95 (s, IH), 9.12 (m, IH), 8.48 (d, IH, J = 6.9 Hz), 8.30 (d, IH, J = 6.9 Hz), 8.24 (d, IH, J = 7.0 Hz), 7.52 (m, 2H), 7.07 (d, 2H, J = 8.6 Hz), 6.99 (d, 2H, J = 8.6 Hz), 6.75 (d, 2H, J = 9.1 Hz), 6.68 (d, 2H, J = 9.1 Hz), 3.98 (m, IH), 3.82 (d, 2H, J = 5.4 Hz), 3.34 (s, IH), 2.6-2.9 (m, 6H). FAB MS mlz 494 (M + 1).

EXAMPLE 24

N-[4-[2-[[(l ,l -dimethylethoxy)carbonyl]amino]ethyl]phenyl]-5-(pyridin-

2-yl -2-thiophenesulfonamide

In a manner analogous to that of Example 5, the title compound was prepared from the Boc amine from Example 4 and 5- (pyridin-2-yl)-2-thiophenesulfonyl chloride: lH NMR (400 MHz, CD3OD) 8.48 (d, IH, J = 5.2 Hz), 7.81 (m, 2H), 7.54 (d, IH, J = 4.1 Hz), 7.41 (m, IH), 7.30 (m, IH), 7.1 1 (s, 4H), 3.18 (t, 2H, J = 7.1 Hz), 2.67 (t, 2H, J = 7.1 Hz), 1.38 (s, 9H). FAB MS mlz 460 (M + 1).

EXAMPLE 25

(S)-N-[4-[2-[[2-hydroxy-3-[[4-[f(l ,l-dimethylethyl)dimethylsilyl]oxy]- phenoxy]propyl]aminolethyl]phenyl]-5-(pyridin-2-yl)-2-thioph ene]- sulfonamide

The Boc amine from Example 24 was deprotected as described in Example 10. In a manner analogous to that of Example 7, the title compound was prepared from the resultant amine and the epoxide from Example 2: lH NMR (400 MHz, CD3OD) 8.48 (d, IH, J = 5.1 Hz), 7.80 (m, 2H), 7.54 (d, IH, J = 4.1 Hz), 7.39 (d, IH, J = 4.1 Hz), 7.30 (m, IH), 7.15 (d, 2H, J = 8.7 Hz), 7.10 (d, 2H, J •= 8.8 Hz), 6.74 (d, 2H, J = 9.0 Hz), 6.67 (d, 2H, J = 9.0 Hz), 3.99 (m, IH), 3.82 (d, 2H, J = 5.4 Hz), 2.7-2.9 (m, 6H), 1.01 (s, 9H), 0.15 (s, 6H).

IS)-N-[4-12-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino] ethyl]- phenvn-5-r2-(pyridin-2-yl thiophene1sulfonamide

In a manner analogous to that of Example 12, the title compound was prepared from the silyl ether from Example 25: lH NMR (400 MHz, CD3OD) 8.48 (m, IH), 7.80 (m, 2H), 7.54 (d, IH, J = 4.0 Hz), 7.40 (d, IH, J = 4.0 Hz), 7.29 (m, IH), 7.13 (d, 2H, J = 8.8 Hz), 7.10 (d, 2H, J = 8.8 Hz), 6.74 (d, 2H, J = 9.1 Hz), 6.68 (d, 2H, J = 9.1 Hz), 3.99 (m, IH), 3.83 (d, 2H, J = 5.4 Hz), 2.7-2.9 (m, 6H). FAB MS /r 526 (M + 1).

EXAMPLE 27

BocNH

N _. -[4-[2-[[(l ,l -dimethylethoxy)carbonyl]amino|ethyl]phenyl]-4-(benzo-

2.1 ,3-thiadiazole sulfonamide

In a manner analogous to that of Example 5, the title compound was prepared from the Boc amine from Example 4 and benzo-2,l ,3-thiadiazole-4-sulfonyl chloride: l H NMR (400 MHz, CDC13) 8.23 (m, 2H), 7.71 (dd, IH, J = 7.1 , 8.7 Hz), 7.04 (m, 4H), 3.16 (m, 2H), 2.65 (t, 2H, J = 7.0 Hz), 1.37 (s, 9H). FAB MS mlz 435 (M + 1).

EXAMPLE 28

(S)-N-[4-[2-[[2-hydroxy-3-[[4-[[(l ,l-dimethylethyl)dimethylsilyl]oxy]- phenoxy]propyl]amino]ethyl]phenyl]-4-(benzo-2,l,3-thiadiazol e)- sulfonamide

The Boc amine from Example 27 was deprotected as described in Example 10. In a manner analogous to that of Example 7, the title compound was prepared from the resultant amine and the epoxide from Example 2: lH NMR (400 MHz, CD3OD) 8.15 (m, 2H), 7.69 (dd, IH, J = 7.2, 8.7 Hz), 6.97 (s, 4H), 6.73 (d, 2H, J = 9.1 Hz), 6.69 (d, 2H, J = 9.1 Hz), 4.88 (m, IH), 3.80 (d, 2H, J = 5.1 Hz), 2.6- 2.85 (m, 6H), 0.99 (s, 9H), 0.14 (s, 6H).

EXAMPLE 29

£S)-N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino ]ethyl]- phenyn-4-(benzo-2.1.3-thiadiazole sulfonamide

In a manner analogous to that of Example 12, the title compound was prepared from the silyl ether from Example 28: l H NMR (400 MHz, CD3OD) 8.18 (m, 2H), 7.69 (dd, IH, J = 7.1 , 8.7 Hz), 6.97 (s, 4H), 6.73 (d, 2H, J = 9.1 Hz), 6.67 (d, 2H, J = 9.1 Hz), 4.89 (m, IH), 3.80 (d, 2H, J = 5.0 Hz), 2.6-2.8 (m, 6H). FAB MS mlz 501 (M + 1), 309.

EXAMPLE 30

N-[4-[2-[(phenylmethoxycarbonyl)amino]ethyl]phenyl]cyclop entane- sulfonamide

Cyclopentanesulfonyl chloride was prepared according to the procedure of S. N. Bhattacharya, et. ah, J. Chem. Soc. (C), 1265- 1267 as follows. To a solution of 2.7 g (1.6 mL, 20 mmol) of sulfuryl chloride in 5 mL of hexane at 0°C was added a solution of 5 mL (10 mmol) of 2 M cyclopentylmagnesium chloride in ether over a 15-min period. The reaction mixture was allowed to warm to room temperature and stir overnight. The mixture was recooled to 0°C and a 5-mL portion of ether was added followed by a 10-mL portion of water. The layers were separated and the organic phase was washed with water, dried over sodium sulfate and concentrated to give 1.12

(70%) of cyclopentanesulfonyl chloride. This compound was used without further purification to prepare the title compound from the Cbz amine from Example 3 in a manner analogous to that of Example 5: lH NMR (400 MHz, CDCI3) δ 7.34-7.30 (m, 5H), 7.13 (s, 4H), 6.44 (br s, IH), 5.07 (s, 2H), 4.74 (br s, IH), 3.50-3.39 (m, 3H), 2:76 (br t, 2H), 2.09-1.91 (m, 4H), 1.86-1.76 (m, 2H), 1.64-1.54 (m, 2H); FAB MS mlz 403 (M + 1).

£S)-N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino ]ethyl]- phenyllcvclopentanesulfonamide

Following the procedures outlined in Examples 6, 7, and 8, the title compound was prepared from the Cbz amine from Example 30: lH NMR (400 MHz, CD3OD) δ 7J9 (s, 4H), 6.75 (d, 2H, J = 9.1 Hz), 6.68 (d, 2H, J = 9.0 Hz), 4.02 (m, IH), 3.85 (d, 2H, J = 5.3 Hz), 3.49 (m, IH), 2.95-2.73 (m, 6H), 2.03-1.86 (m, 4H), 1.79-1.71 (m, 2H), 1.64-1.53 (m, 2H); FAB MS mlz 435 (M + 1).

EXAMPLE 32

(S)-N-[2-[4-(aminophenyl)]ethyl]-2-hydroxy-3-[4-[[( 1 , 1 -Dimethylethyl)- dimethylsilylloxylphenoxylpropylamine

In a manner analogous to that of Example 7, the title compound was prepared from the epoxide from Example 2 and 2-(4-

aminophenyl)ethylamine. Purification by flash chromatography (silica gel, 10% methanol :dichloromethane) gave the title compound: l H NMR (400 MHz, CDCI3) δ 6.97 (d, 2H), 6.72 (s, 4H), 6.61 (d, 2H), 3.98 (m, IH), 3.87 (d, 2H), 3.55 (br s, IH), 2.91 -2.66 (m, 6H), 2.00 (br s, 3H), 0.93 (s, 9H), 0.14 (s, 6H).

EXAMPLE 33

(S)-N-[2-[4-(aminophenyl)]ethyl]-2-hydroxy-3-[4-[[(l ,l-Dimethylethyl)- dimethylsilynoxylphenoxylpropylcarbamic acid 1 J -dimethylethyl ester

To a solution of 2.14 g (1.12 mmol) of amine from Example 32 in 50 mL of THF at 0°C was added a solution of άi-tert- butyldicarbonate in 10 mL of THF. The reaction mixture was stirred at 0°C for 4.5 h, then concentrated. Purification by flash chromatography (silica gel, 40% ethyl acetate :hexanes) gave 2.23 g (84%) of the title compound as an oil: lH NMR (400 MHz, CDCI3) δ 7.00-6.90 (br m, 2H), 6.73 (s, 4H), 6.61 (d, 2H, J = 8.3 Hz), 4.06 (br m, IH), 4.90-4.75 (br m, 2H), 3.44-3.28 (br m, 4H), 2.69 (m, 2H), 1.43 (s, 9H), 0.95 (s, 9H), 0.14 (s, 6H).

EXAMPLE 34

3-Ouinolinesulfonyl chloride

A solution of n-butyllithium (20 mL of 2.5 M in hexanes, 50 mmol) in 250 mL of anhydrous ether was cooled in a dry ice-acetone bath and treated over a 10 min period with a solution of 3-

bromoquinoline (5.0 g, 24 mmol) in 50 mL of ether. The resulting slurry was stirred for 15 min at -78°C, and was then rapidly cannulated into a solution of sulfuryl chloride (7 mL, 100 mmol) in 500 mL anhydrous ether cooled to -78°C. The resulting orange slurry was stirred at -78°C for 30 min, and was then warmed to 0°C over 30 min and concentrated under reduced pressure to a thick semisolid yellow mass, which was partitioned between water and ethyl acetate. After addition of sodium bicarbonate, the aqueous layer was removed and extracted with an additional 50 mL of ethyl acetate. The combined organic extracts were dried over sodium sulfate and concentrated to a yellow oil. Flash chromatography (5%, then 25% EtOAc-hexanes eluant) afforded ca. 2 g of a yellow oil, which crystallized upon standing. Trituration with hexanes gave 250 mg of title compound as a white solid. NMR (400 MHz, d-6 DMSO) 9.42 (d, IH, J = 2.0 Hz), 9.32 (s, IH), 8.45 (d, IH, J = 8.1 Hz), 8.28 (d, IH, J = 8.8 Hz), 8.1 1 (apparent t, IH), 7.94 (apparent t, IH).

EXAMPLE 35

(S)-N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino] ethyl]- phenyll-3-quinolinesulfonamide

To a solution of the TBS-protected aniline from Example 33 (260 mg, 0.50 mmol) and pyridine (50 μL, 0.60 mmol) in 4 mL of methylene chloride was added 3-quinolinesulfonyl chloride (1 18 mg, 0.52 mmol). The red solution was stirred at room temperature for one hour and was concentrated under reduced pressure. The residue was dissolved in 2 mL of methanol, and approximately 5 mL of a 3% solution of HC1 in methanol was added. After stirring at room temperature for 2 h, the solution was concentrated, and the residue was

dissolved in 5 mL of 10% methanolic ammonium hydroxide. After removal of solvent in vacuo, the residue was applied directly to a silica gel column. Elution with 5:4:1 EtOAc:hexanes:10% methanolic NH4OH afforded 186 mg (0.38 mmol, 76% yield) of the title compound as an off-white solid. NMR (400 MHz, CD3OD) 9.02 (d, IH, J = 2.1 Hz), 8.67 (d, IH, J = 2.1 Hz), 8.03 (d, IH, J = 8.6 Hz), 7.97 (d, IH, J = 7.9 Hz), 7.86 (apparent t, IH), 7.66 (apparent t, IH), 7.04 (two overlapping d, 4H), 6.72 (d, 2H, J = 9.1 Hz), 6.67 (d, 2H, J = 9.1 Hz), 3.98 (m, IH), 3.81 (d, 2H, J = 5.4 Hz), 2.84 (m, 3H), 2.72 (m, 3H). FAB MS mlz 494 (M + 1).

EXAMPLE 36

(S _. )-N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino ]ethyl]- phenyl1-4-l(5-methoxycarbonyπpentanoyllamino1benzenesulfona mide

Pyridine 0.314 mL (3.88 mmol) and 4-nitrobenzene- sulfonyl chloride 454.3 mg (2.05 mmol) were added to a solution of BOC protected amine from Example 33 (lg, 1.94 mmol) in dichloromethane at 0°C. Stirring was continued for 2h, before diluting with EtOAc (40 ml), and washing with 3M hydrochloric acid (2 x 10ml), saturated sodium bicarbonate solution (2 x 10ml), and brine (20 ml). The solution was dried over anhydrous magnesium sulphate, concentrated, dissolved in methanol (20 ml), and treated with 20% palladium hydroxide on carbon 350 mg, under an atmosphere of hydrogen for 16h. The reaction was diluted with methanol (60 ml), filtered, concentrated, and purified by flash chromatography (silica gel, 2% methanol/ dichloromethane), to give the amine 888 mg (68%).

To amine, prepared above, 60.5 mg (0.09 mmol) and pyridine 0.016 mL (0.2 mmol) in dichloromethane (0.5 ml) at 0°C, was added a solution of monomethyl adipyl chloride (0J mmol, prepared from monomethyl adipate 0.015 mL (0.1 mmol), oxalyl chloride 0.050 mL (2M solution in dichloromethane, 0J mmol), and DMF (1 drop) in dichloromethane at 0°C for 30min). After lh the reaction was diluted with dichloromethane (10 ml), work up as above and purification by flash chromatography, using the same solvent system as above, yielded the desired amide 67 mg. The material was dissolved in THF (1 ml) and treated with tetrabutylammonium fluoride 0.088 mL (I M in THF, 0.088 mmol). After stirring for 2h, the solution was diluted with EtOAc (10 ml), washed with water (10ml), back extracted with EtOAc (2 x5 ml), washed with brine (10ml), dried with anhydrous magnesium sulphate, concentrated and purified by flash chromatography (silica gel, 5% methanol/dichloromethane) to give the phenol 50 mg (70%).

A portion l lmg (0.0157 mmol) was treated with IM hydrogen chloride in methanol (4.5 ml) at ambient temperature for 20 min, before concentration, and purification by preparative tic (silica gel, 10% methanol (1 % ammonium hydroxide)/dichloromethane) to give the title compound 5 mg (53%). lH NMR (CD3OD) 7.66-7.62 (m, 4H), 7.08 (d, 2H, J=9.6 Hz), 7.01 (d, 2H, J=9.6 Hz), 6.74 (d, 2H, J=9.6Hz), 6.67(d, 2H, J=9.6Hz), 4.03 -3.97(m, IH), 3.84-3.82 (m, 2H), 3.63 (s,3H), 2.90-2.70 (m, 6H), 2.38-2.33 (m, 4H), and 1.72-1.60 (m,4H).

EXAMPLE 37

NHCO(CH ₂ ) ₄ C0 ₂ H

(S)-N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]eth ylj- phenyll-4-r( ^' 5-hvdroxycarbonyl)pentanovnamino1benzenesulfonamide

To the BOC protected phenolic methyl ester from Example 36 90 mg (0J29 mmol) in THF/ water (2ml, 1/1) was added lithium hydroxide monohydrate 27 mg (0.645 mmol), strirring was continued for 16h, before the mixture was neutralised with 3M hydrochloric acid, concentrated, and purified by mplc (35 water (0.1 % TFA)/ 65 methanol) to give the acid 86 mg. A portion 22 mg (0.032 mmol) was treated with trifluoroacetic acid/ dichloromethane (1/1, 2 ml) at ambient temperature for 30min, before concentration, and purification by mplc (60 water (0.1 % TFA)/ 40 methanol) to give the title compound 17 mg (90%). lH NMR (CD3OD) 7.67 (m, 4H), 7.18-7.05 (m, 4H), 6.80- 6.68 (m, 4H), 4.21-4.14 (m, IH), 3.98-3.85 (m, 2H), 3.27-3.10 (m, 4H), 2.95-2.89 (m, 2H), 2.42-2.28 (m, 4H), and 1.73-1.60 (m, 4H).

EXAMPLE 38

NHCONH-nHex

(^-N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]e thyl]- phenyll-4-(hexylaminocarbonylamino benzenesulfonamide

To a suspension of 4-chlorosulphonylbenzene isocyanate 50 mg (0.23 mmol) at -40°C in chloroform (0.5 ml), was added hexylamine 0.23 ml (IM solution in chloroform, 0.23 mmol). Stirring was continued with warming to ambient temperature for 16h, then the mixture was cooled to 0°C and a solution of BOC protected amine from Example 33 (100 mg, 0.193 mmol) in dichloromethane (1 mL), containing pyridine 0.032 mL (0.4 mmol), was added. After 3h the solution was diluted with EtOAc (10 ml), washed with water (10ml), back extracted with EtOAc (2 x5 ml), washed with brine (10ml), dried

with anhydrous magnesium sulphate, concentrated, and purified by preparative tic (silica gel, 2%methanol/ dichloromethane) to give the urea 80 mg. This was treated with IM hydrogen chloride in methanol (4.5 ml) at ambient temperature for 20min, before concentration and purification by preparative tic (silica gel, 15% methanol (1 % ammonium hydroxide)/ dichloromethane) to give the title compound 53.6 mg (47%). lH NMR (CD3OD) 7.58 (d, 2H, J = 8Hz), 7.42 (d, 2H, J = 8Hz), 7.09 (d, 2H, J = 8Hz), 7.01 (d, 2H, J = 8Hz), 6.78-6.65 (m, 4H), 4.06-4.00(m, IH), 3.89-3.80 (m, 2H), 3.15 (t, 2H, J = 7.2Hz), 2.87-265 (m, 6H), 1.53-1.46 (m, 2H), 1.40-1.27 (m, 6H), 0.92-0.88 (m, 3H).

Following the procedures outlined for Examples 1-38, the compounds listed in Tables 1 and 2 were prepared.

TABLE 1

EXAMPLE 127

CbzNH,

Me

NHS0 ₂ Ph

(S)-N-[4-[2-[(phenylmethoxycarbonyl)amino]propyl]phenyl]b enzene- sulfonamide

A slurry of 3.00 g (16.6 mmol) of 4-amino-D-phenyl- alanine hydrate in 100 mL of methanol was heated at relux while gaseous hydrogen chloride was bubbled into the flask. After a 2-h period, the reaction mixture was cooled to room temperature, flushed with nitrogen, and concentrated. The residue was dissolved in 120 mL of a mixture of 140 mL of tetrahydrofuran (THF) and 50 mL of water and treated with 9.15 g (49.8 mmol) of sodium bicarbonate portion wise over a 20-min period. A solution of 18 g of di-fert-butyl dicarbonate in remaining 70 mL of the THF-water mixture was added. The reaction mixture was allowed to stir at room temperature overnight and then was filtered and concentrated. The residue was partitioned between water and dichloromethane. The organic phase was dried over magnesium sulfate and concentrated. Purification by flash chromatography gave 5.17 g (79%) of the corresponding N-Boc methyl ester.

A 4.28-g (10.9 mmol) portion of the above compound was dissolved in 50 mL of THF and treated with 1 1 mL (22 mmol) of a 2 M lithium borohydride solution in THF. After the reaction mixture was allowed to stir overnight, it was quenched by the addition of 5 mL of

saturated aqueous ammonium chloride solution and concentrated. The residue was partitioned between water and ethyl acetate. The aqueous phase was extracted with ethyl acetate and the combined organic phases were dried over magnesium sulfate and concentrated. The resultant material was dissolved in 50 mL of dichloromethane, cooled to 0°C, and treated with 1.8 mL of triethylamine and 0.90 mL of methanesulfonyl chloride. After the reaction mixture was allowed to stir at 0°C for 1 h, it was washed sequentially with 5% aqueous hydrochloric acid and saturated aqueous sodium bicarbonate, dried over magnesium sulfate, and concentrated. The resultant semisolid was immediately dissolved in 150 mL of dichloromethane and treated with 30 mL of trifluoroacetic acid. After 1.5 h, the solution was concentrated. The residue was dissoved in 70 mL of ethanol and 5.0 g (49 mmol) of sodium acetate was added. The mixture was stirred over 1 g of 20% palladium hydroxide on carbon under hydrogen at 30 psi for 24 h. It was filtered through Celite and concentrated. Flash chromatography (4:1 dichloromethane: 10% concentrated ammonium hydroxide in methanol) to give 2.01 g of (25)-l -(4-aminophenyl)propyl-2-amine.

A 451 mg (3.0 mmol) portion of the above compound was dissolved in 20 mL of chloroform and 2 mL of DMF and cooled to 0°C. Triethylamine (304 mg, 0.420 mL, 3.0 mmol) was added followed by 512 mg (0.428 mL, 3.0 mmol) of benzyl chloroformate, dropwise. The reaction mixture was allowed to stir at 0°C for 2 h and then allowed to warm to room temperature overnight. It was then partitioned between ethyl acetate and water. The organic phase was dried over magnesium sulfate and concentrated. Purification by flash chromatography (silica gel, 50% ethyl acetate/hexanes) gave 138 mg of the corresponding N- Cbz derivative. This compound was treated with benzenesulfonyl chloride according to the procedure described in Example 5 to give the title compound: lH NMR (400 MHz, CDC13) 7.70 (d, 2H, J = 7.5 Hz), 7.2-7.5 (m, 8H), 7.00 (d, 2H, J = 8.2 Hz), 6.93 (d, 2H, J = 8.2 Hz), 6.48 (s, IH), 5.03 (s, 2H), 4.51 (m, IH), 3.88 (m, IH), 2.73 (m, IH), 2.60 (dd, IH, J = 6.8, 13.5 Hz), 1.55 (s, IH), 1.04 (d, 3H, J = 6.7 Hz). FAB MS mlz 425 (M + 1 ).

EXAMPLE 128

(S _Λ S)-N-f4-[2-f[2-hydroxy-3-[(4-phenylmethoxy)phenoxy]pro pyl]- aminolpropynphenyllbenzenesulfonamide

The Cbz amine from Example 127 was deprotected as described in Example 6. In a manner analogous to that of Example 7, the title compound was prepared from the resultant amine and the epoxide from Example 1 : lH NMR (400 MHz, CD3OD) 7.70 (d, 2H, J = 7.1 Hz), 7.52 (m, IH), 7.2-7.5 (m, 7H), 7.06 (d, 2H, J = 8.6 Hz), 7.00 (d, 2H, J = 8.6 Hz), 6.75 (d, 2H, J = 9.0), 6.68 (d, 2H, J = 9.0 Hz), 5.02 (s, 2H), 3.95 (m, IH), 3.83 (d, 2H, J = 5.1 Hz), 2.85 (m, 2H), 2.67 (dd, IH, J = 6.8, 13.2 Hz), 2.56 (m, 2H), 1.03 (d, 3H, J = 6.3 Hz). FAB MS

EXAMPLE 129

(SiS)-N-[4-[2-[f2-hydroxy-3-(4-hydroxyphenoxy)propyl]amin o]- propyllphenyllbenzenesulfonamide

In a manner analogous to that of Example 8, the title compound was prepared from the benzyl ether from Example 128: lH NMR (400 MHz, CD3OD) 7.71 (d, 2H, J = 7.2 Hz), 7.52 (m, IH), 7.43 (m, 2H), 7.06 (d, 2H, J = 8.6 Hz), 7.00 (d, 2H, J = 8.6 Hz), 6.75 (d, 2H, J = 9.0), 6.68 (d, 2H, J = 9.0 Hz), 3.93 (m, IH), 3.82 (d, 2H, J = 5.2

Hz), 2.88 (m, 2H), 2.66 (dd, IH, J = 6.6, 13.2 Hz), 2.57 (m, 2H), 1.04 (d, 3H, J = 6.3 Hz). FAB MS mlz 457 (M + 1 ).

EXAMPLE 130

_(S)-N-[4-[2-f[2-hydroxy-3-(4-hydroxyphenoxy)propyl]am phenyll-4-aminobenzenesulfonamide

A solution of 67 mg (0.14 mmol) of nitro derivative from Example 54 in 5 mL of methanol was stirred over 20% palladium hydroxide on carbon under an atmosphere of hydrogen for 30 min. The reaction mixture was filtered and concentrated to give 36 mg (59%) of the title compound: lH NMR (400 MHz, CD3OD) δ 7.39 (d, 2H, J = 8.8 Hz), 7.08 (d, 2H, J = 8.5 Hz), 7.00 (d, 2H, J = 8.5 Hz), 6.75 (d, 2H, J = 9.1 Hz), 6.68 (d, 2H, J = 9.0 Hz), 6.56 (d, 2H, J = 8.8 Hz), 4.04 (m, IH), 3.89-3.82 (overlapping dd, 2H), 2.97-2.77 (m, 6H).

EXAMPLE 131

(S)-2-phenoxymethyloxirane

The title compound was prepared from phenol in a manner analogous to that of Example 1 : lH NMR (400 MHz, CDCI3) δ 7.28 (t, 2H), 6.96 (t, IH), 6.91 (d, 2H), 4.20 (dd, IH), 3.96 (dd, IH), 3.34 (m, lH), 2.90 (t, IH), 2.73 (dd, IH).

EXAMPLE 132

(S)-N-r2-[4-(aminophenyl 1ethyl1-2-hvdroxy-3-phenoxypropylamine

In a manner analogous to that of Example 7, the title compound was prepared from the epoxide from Example 131 and 2-(4- aminophenyl)ethylamine: lH NMR (400 MHz, CDCI3) δ 7.25 (t, 2H, J = 8.0 Hz), 6.97 (d, 2H, J = 8.4 Hz), 6.93 (t, IH, J = 7.4 Hz), 6.87 (d, 2H, J = 7.8 Hz), 6.61 (d, 2H, J = 8.4 Hz), 4.00 (m, IH), 3.93 (d, 2H, J = 5.4 Hz), 3.57 (br s, IH), 2.90-2.71 (m, 6H), 1.85 (br s, 3H).

EXAMPLE 133

(S _. )-N-[2-[4-(aminophenyl)]ethyl]-2-hydroxy-3-phenoxyprop ylcarbamic acid 1.1-dimethylethyl ester

In a manner analogous to that of Example 33, the title compound was prepared from the amine from Example 132 and di-tert- butyldicarbonate: lH NMR (400 MHz, CDCI3) δ 7.26 (t, 2H, J = 8.0 Hz), 6-96-6.87 (m, 5H), 6.59 (d, 2H, J = 8.4 Hz), 4.10 (br m, IH), 3.94 (br m, IH), 3.84 (br m, IH), 3.56 (br s, IH), 3.45-3.20 (m, 4H), 2.78 (br m, 2H), 1.55 (br s, 3H), 1.43 (s, 9H).

EXAMPLE 134

(S _. )-N-[4-[2-[(2-hydroxy-3-phenoxypropyl)amino]ethyl]-phe nyl]-4- chlorobenzenesulf onamide

To a solution of the BOC-protected aniline from Example 133 (96 mg, 0.25 mmol) and pyridine (50 μL, 0.6 mmol) in 5 mL of methylene chloride was added 4-chlorobenzenesulfonyl chloride (57 mg, 0.27 mmol). The reaction mixture was stirred at room temperature under nitrogen atmosphere overnight. The red solution was concentrated under vacuum and the residue was purified by preparative thin layer chromatography on silica gel (eluant 2:3 ethyl acetate/hexanes) to give 133 mg (98%) of an off-white solid. This N- BOC sulfonamide (130 mg, 0.227 mmol) was dissolved in 3 mL of methylene chloride and 1 mL of trifluoroacetic acid was added. After stirring at room temperature for lh, the solution was concentrated and the residue was purified by preparative thin layer chromatography on silica gel (eluant 10:90:1 methanol/methylene chloride/30% ammonium hydroxide) to give 130 mg (99%) of the title compound. lH NMR (400 MHz, CD3OD) δ 7.71 (d, 2H, J = 9Hz), 7.47 (d, 2H, J = 9Hz), 7.27 (t, 2H, J = 9Hz), 7.16 (d, 2H, J = 8.5Hz), 7.07 (d, 2H, J = 8.5Hz), 6.94 (dd, 3H), 4.22 (m, IH), 3.99 (m , 2H), 3.21 (m, 3H), 2.94 (m, 2H).

Following the procedures outlined for Examples 131 -134, the compounds listed in Table 3 were prepared.

TABLE 3

5

0

EX AMPLE 141

(S)-2-r(4-Fluorophenoxy)methyl loxirane

The title compound was prepared from 4-fluorophenol in a manner analogous to that of Example 1 : NMR (400 MHz, CDCI3) 6.95 (m, 2H), 6.84 (m, 2H), 4.17 (dd, IH, J = 3.0, 1 1.0 Hz), 3.88 (dd, I H, J = 5.7, 1 1.0 Hz), 3.33 (m, IH), 2.88 (m, I H), 2.73 (dd, IH, J = 2.6, 5.0 Hz).

EXAMPLE 142

£S)-N-f4-[2-[[3-(4-fluorophenoxy)-2-hydroxypropyl]am phenyllbenzenesulf onamide

In a manner analogous to that of Example 7, the title compound was prepared from the amine from Example 6 and the epoxide from Example 141 : lH NMR (300 MHz, CD3OD): 2.93 (m, 2H), 3.1 -3.28 (m, 4H), 3.96 (m, 2H), 4.2 (m, IH), 6.9-7.16 (m, 8H), 7.5 (m, 3H), 7.74 (d, J = 7Hz, IH); FAB-MS mlz 445 (M + 1).

Following the procedures outlined for Examples 141 -142, the compounds listed in Table 4 were prepared.

EXAMPLE 150

(S)-2-I13-Cyanophenoxy1methyl1oxirane

The title compound was prepared from 3-cyanophenol in a manner analogous to that of Example 1 : NMR (400 MHz, CDCL3) δ 7.35 (t, IH), 7.24 (d, IH), 7.13 (m, 2H), 4.27 (dd, I H, J = 2.7, l l .l Hz), 3.89 (dd, IH, J = 6.0, 11.1 Hz), 3.33 (m, IH), 2.90 (t, IH), 2.75 (dd, lH, J = 2.6, 4.8Hz).

EXAMPLE 151

(S)-N-[4-[2-[[2-Hydroxy-3-(3-cyanophenoxy)propyl]amino]et hyl]- phenyllamine

In a manner analogous to that of Example 7, the title compound was prepared from 2-(4-aminophenyl)ethylamine and the epoxide from Example 150: NMR (400 MHz, CD3OD) δ 7.44 (t, IH), 7.27 (m, 3H), 6.97 (d, 2H, J = 8.5Hz), 6.67 (d, 2H, J = 8.4Hz), 4.04 (m, IH), 3.97 (m, 2H), 2.81 (m, 3H), 2.71 (m, 3H).

EX AMPLE 152

(jS)-N-[2-|4-(Aminophenyl)]ethyl]-2-hydroxy-3-(3-cyanophe noxy)- propylcarbamic acid l J -dimethylethyl ester

In a manner analogous to that of Example 33, the title compound was prepared from the amine in the previous Example 151 and di-ferr-butyldicarbonate: NMR (400 MHz, CD3OD) δ 7.44 (t, IH), 7.27 (m, 3H), 6.99 (d, 2H), 6.65 (d, 2H), 4.08 (m, IH), 3.92 (m, 2H), 3.43 (m, 3H), 3.15 (m, IH), 2.70 (t, 2H), 1.42 (s, 9H).

EXAMPLE 153

(S)-N-[4-[2-[[2-Hydroxy-3-(3-cyanophenoxy)propyl]amino]et hyl]- phenyπ-3-quinolinesulfonamide

In a manner analogous to that of Example 134, the title compound was prepared from the amine from Example 152 and 3- quinolinesulfonyl chloride from Example 34. The crude product treated with trifluoroacetic acid to remove Boc group: NMR (400 MHz, CD3OD) δ 9.01 (d, IH, J = 2.2Hz), 8.69 (d, IH, J = 2.2Hz), 8.05 (dd, 2H), 7.90 (t, 2H), 7.70 (t, IH), 7.42 (t, IH), 7.26 (m, 3H), 7.06

(dd, 4H, J =8 .6, 21.6 Hz), 4.03 (m, IH), 3.96 (m, 2H), 2.82 (m, 3H), 2.73 (m, 3H). FAB-MS mlz 503 (M+l ).

EXAMPLE 154

3-Cvano-4-nitrophenol

To a 0°C solution of 578 mg (2.28 mmol) 5-phenyl- methoxy-2-nitrobenzonitrile, prepared according to the procedure of E. Elslager, et. al-, J- Heterocyclic Chem. 1972, 9, 759-773, in 5 mL of dichloromethane at 0°C was added 2.6 mL (2.62 mmol, 1.15 equiv) of a 1.0 M solution of boron tribromide in dichloromethane. After the reaction mixture was stirred for 3 h, it was diluted with ethyl acetate, washed sequentially with 1 N aqueous sodium hydrogen sulfate solution and saturated aqueous sodium chloride solution, dried over magnesium sulfate and concentrated to give 357 mg (96%) of the title compound which was used without further purification: l H NMR (400 MHz, CD3OD) δ 8.17 (d, IH, J = 9.2 Hz), 7.03 (d, IH, J = 2.7 Hz), 6.92 (dd, IH, J = 2.7, 9.3 Hz).

(S)-2-r(3-Cyano-4-nitrophenyl)methyl1oxirane

To a solution of 357 mg (2.18 mmol) of 3-cyano-4- nitrophenol from Example 154 in 5 mL of DMF at 0°C was added 91.0 mg (2.28 mmol) of sodium hydroxide as a 60% dispersion in oil. After the mixture was allowed to stir for 30 min, a solution of 513 mg (1.98 mmol) of (2S)-glycidyl 3 -nitrobenzene sulfonate in 10 mL of DMF was

added via cannula. The reaction mixture was allowed to warm to room temperature and then heated at 55 °C overnight. The reaction was cooled, quenched by the addition of saturated aqueous ammonium chloride solution, and poured into ethyl acetate. The organic phase was washed sequentially with two portions of water and one portion of saturated aqeous sodium chloride solution. The organic phase was dried over magnesium sulfate and concentrated. Purification by flash chromatography (silica, 40% ethyl acetate/hexanes) gave 287 mg (66%) of the title compound as a yellow solid: 1 H NMR (400 MHz, CDCI3) δ 8.29 (d, IH, J = 9.2 Hz), 7.36 (d, IH, J = 2.8 Hz), 7.25 (dd, IH, J = 2.8, 9.2 Hz), 4.47 (dd, IH, J = 2.3, 1 1.3), 4.00 (dd, IH, J = 6.2, 1 1.4 Hz), 3.37 (m, IH), 2.95 (t, IH, J = 4.3 Hz), 2.77 (dd, IH, J = 2.6, 4.7 Hz).

EXAMPLE 156

(£)-N-[4-[2-[13-(4-Amino-3-cyanophenoxy)-2-hydroxypropyl ]amino]- ethyllphenyllbenzenesulfonamide

A solution of 75 mg (0.341 mmol) of the epoxide from Example 155 and 122 mg (0.443 mmol, 1.3 equiv) of amine from Example 6 were heated in methanol at reflux overnight. The mixture was concentrated. Purification by flash chromatography (silica, 5% methanol: dichloromethane) gave 48 mg (28%) of the resultant amino alcohol. This was dissoved in ethanol and treated with 10% palladium on carbon under an atmosphere of hydrogen for 6 h. The reaction mixture was filtered and concentrated. Purification by flash chromatography (silica, 5% 10: 1 methanol: concentrated aqueous ammonium hydroxide in dichloromethane) gave 15 mg of the title compound: lH NMR (400 MHz, CDCI3) δ 7.71 (d, 2H, J = 7.2 Hz), 7.53 (t, IH, J = 7.4 Hz), 7.44 (t, 2H, J = 7.6 Hz), 7.07 (d, 2H, J = 8.6

Hz), 7.01-6.98 (m, 3H), 6.90 (d, IH, J = 2.8 Hz), 6.77 (d, IH, J = 9.0 Hz).

EXAMPLE 157

(S)-M-[4-[2-[[3-(4-Amino-3-cyanophenoxy)-2-hydroxypropyl] amino]- ethyll-phenyn-3-quinolinesulfonamide

In a manner analogous to that of Example 156, the title compound was prepared from the epoxide from Example 155 and N-[4- (2-aminoethyl)phenyl] -3 -quinolinesulf onamide: lH NMR (400 MHz, CD3OD) δ 9.01 (d, IH, J = 2.3 Hz), 8.69 (d, IH, J = 2.3 Hz), 8.06 (d,

IH, J = 8.5 Hz), 8.02 (d, IH, J = 8.5 Hz), 7.90 (m, IH), 7.70 (m, IH), 7.11 (d, 2H), 7.04 (d, 2H), 6.98 (dd, IH), 6.89 (d, IH, J = 3.0 Hz), 6.76 (d, IH, J = 9.0 Hz), 3.98 (m, IH), 3.82 (d, 2H, J = 5.5 Hz), 2.91-2.71 (m, 6H).

EXAMPLE 158

(S -2-ri3-(Hvdroxymethyl phenoxy1methylloxirane

The title compound was prepared from 3-hydroxybenzyl alcohol in a manner analogous to that of Example 1 : NMR (400 MHz, CDCL3) δ 7.26 (m, IH), 6.94 (m, 2H), 6.82 (d, IH), 4.65 (s, 2H), 4.22 (dd, IH, J = 3.2, 11.0 Hz), 3.95 (dd, IH, J = 5.6, 10.7 Hz), 3.33 (m, IH), 2.90 (t, IH), 2.75 (m, IH).

EXAMPLE 159

(S)-N-[4-[2-[r2-Hydroxy-3-[(3-hydroxymethyl)phenoxy]propy l]amino]- ethyllphenyl lamine

In a manner analogous to that of Example 7, the title compound was prepared from 2-(4-aminophenyl)ethylamine and the epoxide from Example 158 above: NMR (400MHz, CD3OD) δ 7.22 (t, IH), 6.98 (d, 2H, J = 4.4Hz), 6.96 (d, 2H), 6.81 (d, IH), 6.67 (d, 2H, J = 4.4 Hz), 4.56 (s, 2H), 4.08 (m, IH), 3.92 (d, 2H, J = 5.4 Hz), 2.90 (m, 3H), 2.71 (m, 3H).

EXAMPLE 160

(S)-N-[2-f4-(Aminophenyl)]ethyl]-2-hydroxy-3-[(3-hydroxym ethyl)- phenoxylpropylcarbamic acid 1.1 -dimethylethyl ester

In a manner analogous to that of Example 33, the title compound was prepared from the amine from Example 159 and di-tert- butyldicarbonate: NMR (400MHz, CD3OD) δ 7.21 (t, IH), 7.09 (m, IH), 6.92 (m, 3H), 6.81 (m, IH), 6.66 (d, 2H), 4.57 (s, 2H), 4.07 (m,

1H), 3.89 (m, 2H), 3.43 (m, 2H), 3.20 (m, 2H), 2.69 (t, 2H), 1.40 (s, 9H).

EXAMPLE 161

(S)-N-[4-[2-[[2-Hydroxy-3-[(3-hydroxymethyl)phenoxy]propy l]aminoJ- ethyllphenyn-3-quinolinesulfonamide

In a manner analogous to that of Example 134, the title compound was prepared from the amine from Example 160 and 3- quinolinesulfonyl chloride from Example 34. The crude product was treated with trifluoroacetic acid to remove the Boc group: NMR (400 MHz, CD3OD) δ 9.01 (d, IH, J = 2.3Hz), 8.68 (d, IH, J = 2.3Hz), 8.04 (dd, 2H), 7.91 (t, 2H), 7.69 (t, IH), 7.21 (t, IH), 7.06 (q, 4H), 6.91 (ran, 2H), 6.79 (m, IH), 4.55 (s, 2H), 4.03 (m, IH), 3.91 (d, 2H, J = 6.6Hz), 2.87 (m, 3H), 2.78 (m, 3H). FAB-MS mlz 508 (M+l ).

EXAMPLE 162

(SV2-(3-pyridyloxymethyPoxirane

To a solution of 1 1.9 g (0.125 mol) of 3-hydroxypyridine in 50 mL of DMSO at 15°C was added 120 mL (0.12 mol) of a 1.0 M solution of sodium hexamethyldisilylazide in THF. After the reaction mixture was allowed to stir for 5 min, 25.9 g (0.10 mol) of (2S glycidyl 3 -nitrobenzene sulfonate was added in one portion. The

mixture was cooled with a room temperature water bath for 30 min. It was then quenched by the addition of 250 mL of water and extracted with three portions of ethyl acetate. The combined aqueous extracts were washed sequentially with water and brine, dried over sodium sulfate, treated with granular charcoal, filtered and concentrated to give 7.7 g (51 %) of an orange oil which was used without further purification. An analytical sample was prepared by flash chromatography (silica gel, 80% ethyl acetate/hexane): lH NMR (400 MHz, CDC13) δ 8.31 (m, IH), 8.21 (m, IH), 7.20-7.22 (m, 2H), 4.29 (dd, IH, J = 1 ,6 Hz), 3.95 (m, IH), 3.34 (m, I H), 2.90 (t, IH, J = 3Hz), 2.75 (m, IH).

EXAMPLE 163

(£)-N-[2-[4-(nitrophenyl)]ethyl]-2-hydroxy-3-pyridinylox ypropyl- carbamic acid 1 Λ -dimethylethyl ester

A solution of 34.6 g (0.224 mol) of epoxide from Example 162 in 300 mL of anhydrous methanol was treated with 38 mL (0.275 mol) of triethylamine and 55.7 g (0.275 mol) of 4-nitrophenethylamine hydrochloride. The solution was heated at reflux for 10 h, then cooled to room temperature and concentrated. The resultant mixture was suspended in 500 mL of dichloromethane and treated with 1 15 g of di- fert-butyldicarbonate in three portions (90 g, 15 g, 10 g) over 4 h. The reaction mixture was stirred overnight. Dilute brine was added and the mixture was extracted three times with dichloromethane. The combined organic extracts were dried over sodium sulfate and concentrated. Purification by flash chromatography (silica gel, 50%, 75%, 100% ethyl acetate/hexane) gave 38.0 g of the title compound: lH NMR (400 MHz, CD3OD) δ 8.23 (d, IH, J = 4Hz), 8.12 (dd, IH, J = 2.4Hz),

7.7 l (d, 2H, J = 8Hz), 7.52 (m, IH), 7.40-7.48 (m, 3H), 7.35 (m, IH),

7.09 (d, 2H, J = 10Hz), 7.00 (d, 2H, J = lOHz), 3.95-4.08 (m, 3H), 2.69- 2.90 (m, 6H).

EXAMPLE 164

(S)-N-[2-[4-(Aminophenyl)]ethyl]-2-hydroxy-3-l(pyridin-3- yl)oxy]- propylcarbamic acid 1.1-dimethylethyl ester

A 37.8-g (0.09 mol) portion of the nitro compound from Example 163 was dissolved in 300 mL of ethyl acetate and hydrogenated over 7.1 g of 20 % palladium hydroxide on carbon overnight. The mixture was filtered and concentrated to give the title compound, which was used without further purification.

EXAMPLE 165

(S)-N-[4-[2-[[2-hydroxy-3-(3-pyridyloxy)propyl]amino]ethy l]- phenyllbenzenesulfonamide

In a manner analogous to that of Example 7, the title compound was prepared from the epoxide from Example 162 and N-[4- (2-aminoethyl)phenyl]benzenesulfonamide (Example 6). Purification by preparative thin layer chromatography on silica gel (eluant 90:10:2 methylen chloride/methanol/30% ammonium hydroxide) gave the title compound. lH NMR (400 MHz, CD3OD) δ 8.23 (d, IH, J = 4Hz), 8.12 (dd, IH, J = 2.4Hz), 7.7 l(d, 2H, J = 8Hz), 7.52 (m, IH), 7.40-7.48 (m,

3H), 7.35 (m, IH), 7.09 (d, 2H, J = lOHz), 7.00 (d, 2H, J = lOHz), 3.95- 4.08 (m, 3H), 2.69-2.90 (m, 6H).

EXAMPLE 166

(S)-N-[4-[2-[[2-hydroxy-3-(3-pyridyloxy)propyljamino]ethy l]-phenyl]-

3-quinolinesulfonamide

To a solution of the aniline (1.0 g, 2.60 mmol) from Example 164 and pyridine (0.21 mL, 2.60 mmol) in 15 mL of methylene chloride was added 3-quinolinesulfonyl chloride (590 mg, 2.60 mmol) from Example 34. The pink solution was stirred at room temperature for 1.5 h and was concentrated under reduced pressure. The residue was dissolved in 20 mL of methanol, and approximately 8 mL of a 6N HCl was added. After warming at reflux for 18 h, the cooled solution was concentrated in vacuo, and the residue was dissolved in 10 mL of 10% methanolic ammonium hydroxide. After removal of solvent in vacuo, the residue was applied directly to a silica gel column. Elution with 9:1 CH2Cl2:10% methanolic NH4OH afforded 0.84 g (1.78 mmol, 68% yield) of the title compound as an yellow solid. NMR (400 MHz, CD3OD) 9.01 (d, IH, J = 2.2 Hz), 8.75 (d, IH, J = 2.2 Hz), 8.22 (d, IH, J = 2.9 Hz), 8.12 (dd, IH, J = 1.3, 4.7 Hz), 8.07 (d, IH, J = 8.6 Hz), 8.04 (d, IH, J = 8.6 Hz), 7.93 (apparent t, IH), 7.72 (apparent t, IH), 7.41 (m, IH), 7.35 (dd, IH, J = 4.7, 7.5 Hz). FAB MS mlz 479 (M + 1).

NHCOPh

(S _. )-N-[4-[2-[[2-hydroxy-3-(3-pyridyloxy)propyl]amino]eth ylJ-phenyl l- 4-benzamidobenzenesulfonamide

To a solution of 1.00 g (2.58 mmol) of Boc aniline derivative from Example 164 and 0.25 mL (3J0 mmol, 1.2 equiv) of pyridine in dichloromethane at 0°C was added a solution of 572 mg (2.58 mmol) of 4-nitrobenzenesulfonyl chloride in 25 mL of dichloromethane via cannula. The reaction mixture was allowed to stir at 0°C for 1.5 h, then concentrated. Purification by flash chromatography (silica gel, ethyl acetate) gave 1.22 g (84%) of the resultant nitrobenzene sulfonamide. An 820-mg portion was dissolved in 15 mL of ethyl acetate and stirred over 20% palladium hydroxide on carbon under an atmosphere of hydrogen overnight. The reaction mixture was then filtered and concentrated. Purification by flash chromatography (silica, ethyl acetate) gave 636 mg (80%) of the corresponding 4-aminosulfonamide. A 203-mg (0.374 mmol) portion was dissolved in 4 mL of dichloromethane and treated with 36 mg (0.036 mL, 0.45 mmol) of pyridine and 58 mg (0.048 mL, 0.41 mmol) of benzoyl chloride. The reaction mixture was allowed to stir at 0°C for 45 min, and then 4 mL of trifluoroacetic acid was added. After 30 min, the reaction was concentrated. Purification by flash chromatography (silica, 7.5 % 10:1 methanol: concentrated aqueous ammonium hydroxide in dichloromethane) gave 144 mg (70%) of the title compound: l H NMR (400 MHz, CD3OD) δ 8.21 (d, IH, J = 2.9

Hz), 8.1 1 (dd, IH, J = 1.3, 4.6 Hz), 7.90 (d, 2H, J = 7.0 Hz), 7.82 (d, 2H, J = 8.9 Hz), 7.69 (d, 2H, J = 8.9 Hz), 7.58 (t, IH, J = 7.4 Hz), 7.49 (t, 2H, J = 7.4 Hz), 7.40 (ddd, IH, J = 1.3, 2.9, 8.5 Hz), 7.34 (dd, IH, J

= 4.5, 8.9 Hz), 7.10 (d, 2H, J = 8.5 Hz), 7.02 (d, 2H, J = 8.5 Hz), 4.06- 3.95 (m, 3H), 2.86-2.69 (m, 6H).

Following the procedures outlined for Examples 162-167, the compounds listed in Tables 5 and 6 were prepared.

TABLE 5

EXAMPLE 185

(S -2-iπ 2-(4-nitrobenzenazo)-5-pyridinyl loxylmethyl loxirane

The title compound was prepared from 5-hydroxy-2-(4- nitrobenzenazo)pyridine (J. A. Moore and F. J. Marascia, J. Amer. Chem. Soc, 81, 6049-6056 (1959)) in a manner analogous to that of Example 1 : lH NMR (400 MHz, CDCI3) δ 8.45 (s, IH), 8.37 (d, 2H, J = 9.0 Hz), 8.1 1 (d, 2H, J = 9.0 Hz), 7.94 (d, IH, J = 8.6 Hz), 7.45 (dd, IH, J = 2.9, 8.8 Hz), 4.46 (dd, IH, J = 2.5, 1 1 Hz), 4.06 (dd, IH, J = 6.0, 1 1 Hz), 3.41 (m, IH), 2.96 (t, IH, J = 4.4 Hz), 2.80 (dd, IH, J = 2.6, 4.6 Hz).

EXAMPLE 186

£S)-N-[4-[2-[[2-hydroxy-3-[[2-(4-nitrobenzenazo propynaminolethyllphenyll-2-naphthalenesulfonamide

The Cbz amine from Example 13 was deprotected as described in Example 6. In a manner analogous to that of Example 7, the title compound was prepared from the resultant amine and the epoxide from Example 185: lH NMR (400 MHz, CD3OD) δ 8.43 (d, 2H, J = 9.0 Hz), 8.38 (d, IH, J = 2.9 Hz), 8.28 (d, IH, J = 1.8 Hz), 8.13 (d, 2H, J = 9.0 Hz), 7.98 (d, IH, J = 9.0 Hz), 7.93-7.88 (m, 3H), 7.72

(dd, IH, J = 1.8, 8.7 Hz), 7.63-7.54 (m, 3H), 7.07 (d, 2H, J = 8.7 Hz), 7.03 (d, 2H, J = 8.7 Hz), 4.16-4.06 (m, 3H), 2.88-2.71 (m, 6H); FAB MS mlz 627 (M + 1).

EXAMPLE 187

{^-N-[4-12-[[3-l(2-amino-5-pyridinyl)oxy]-2-hydroxypropyl ]amino]- ethyllphenyn-2-naphthalenesulfonamide

A solution of 31.1 mg (0.0496 mmol) of the benzenazo derivative from Example 186 in 2 mL of acetic acid and 2 mL of methanol was stirred over 20% palladium hydroxide on carbon under an atmosphere of hydrogen for 1 h. It was then filtered and concentrated. Purification by flash chromatography (silica gel, 10% 10: 1 methanohconcentrated ammonium hydroxide in dichloromethane) gave 19.0 mg (78%) of the title compound: lH NMR (400 MHz, CD3OD) δ 8.27 (d, IH, J = 1.8 Hz), 7.93-7.87 (m, 3H), 7.72 (dd, IH, J = 1.8, 8.7 Hz), 7.62-7.54 (m, 3H), 7.17 (dd, IH, J = 3.0, 9.0 Hz), 7.06- 7.01 (overlapping d, 4H), 6.55 (d, IH, J = 9.2 Hz), 3.95 (m, IH), 3.86- 3.79 (overlapping dd, 2H), 2.82-2.63 (m, 6H); FAB MS mlz 493 (M + l ).

EXAMPLE 188

2-Acetamido-5-hvdroχypyridine

A mixture of 1.72 g (10.4 mmol) of 2-acetamido-5- methoxypyridine, prepared according to the procedure of J.

Lombardino, J. Med. Chem. 1981, 24, 39-42, and 2.54 g (51.8 mmol) of sodium cyanide in 10 mL of DMSO was heated at 165°C under nitrogen for 48 h. The mixture was concentrated under vacuum to remove the DMSO. Purification by flash chromatography (silica, crude product transferred to column in methanol, then diluted With dichloromethane and eluted with 10% 10:1 methanohconcentrated aqueous ammonium hydroxide in dichloromethane) gave 0.881 g (56%) of the title compound as a brown solid: l H NMR (400 MHz, CD3OD) δ 7.84-7.81 (overlapping d, 2H), 7.19 (dd, IH, J = 2.9, 8.9 Hz), 2.12 (s, 3H).

EXAMPLE 189

rSV2-[(2-Acetamidopyridin-5-vDmethyl1oxirane

To a solution of 842 mg (5.53 mmol) of 2-acetamido-5- hydroxypyridine from Example 188 in 15 mL of DMF at 0°C was added 221 mg (5.53 mmol) of sodium hydroxide as a 60% dispersion in oil. After the mixture was allowed to stir for 30 min, 1.58 g (6.09 mmol, 1.1 equiv) of (2S)-glycidyl 3 -nitrobenzene sulfonate was added. The reaction mixture was stirred at room temperature for 4 h, then partitioned between 400 mL of ethyl acetate and 100 mL of saturated aqeous sodium chloride solution. The aqueous layer was washed with 100 mL of ethyl acetate. The combined organic phases were dried over magnesium sulfate and concentrated under high vacuum to remove DMF. Purification by flash chromatography (silica, 80% ethyl acetate/hexane) gave 716 mg (62%) of the title compound as a crystalline solid: lH NMR (400 MHz, CDCI3) δ 8.1 1 (d, IH, J = 9.1 Hz), 7.98 (br s, IH), 7.95 (d, IH, J = 2.9 Hz), 4.26 (dd, IH, J = 2.9, 1 1.0 Hz), 3.92 (d, IH, J = 5.8, 1 1.0 Hz), 3.33 (m, I H), 2.90 (t, 1H, J = 4.5 Hz), 2.74 (dd, IH, J = 2.6, 4.8 Hz), 2.16 (s, 3H).

EXAMPLE 190

(S _. )-N-[2-[4-(Aminophenyl)]ethyl]-2-hydroxy-3-[(2-acetami dopyridin-5- yPoxylpropylcarbamic acid 1.1 -dimethylethyl ester

In a manner analogous to that of Examples 163 and 164, the title compound was prepared from the epoxide from Example 189: l H NMR (400 MHz, CD3OD) δ 7.93-8.02 (m, 2H), 7.38 (d, IH, J = 8Hz), 6.89-6.98 (m, 2H), 6.66 (d, 2H, 10 Hz), 4.06 (m, I H), 3.89-4.00 (m, 2H), 3.38-3.50 (m, 3H), 3.14 (m, IH), 2.70 (t, 2H,J = 8Hz), 2.13 (s, 3H), 1.41 (s, 9H).

EXAMPLE 191

(S)-N-[4-[2-[[3-[(2-ammo-5-pyridinyl)oxy]-2-hy ethyll-phenvn-4-isopropylbenzenesulfonamide

To a solution of the BOC-protected aniline from Example 190 (1.16 g, 2.6 mmol) and pyridine (300 μL, 3.64 mmol, 1.4 eq) in 45 mL of methylene chloride was added 4-isopropylbenzenesulfonyl chloride (577 mg, 2.6 mmol). The reaction mixture was stirred at room temperature under nitrogen atmosphere overnight. The pink solution was poured into brine (20 mL) and the organics were extacted with methylene chloride. The solution was washed with saturated ammonium chloride solution, water and brine and then dried over anhydrous magnesim sulfate. The solution was filtered and

concentrated under vacuum. Purification by flash column chromatography (silica gel, ethyl acetate) gave 1.54 g (94.5%) of the corresponding N-acetyl derivative: lH NMR (400 MHz, CD3OD) δ 7.94-8.00 (m, 2H), 7.60-7.67 (m, 2H), 7,37 (d, I H, J = 10 Hz), 7.31 (d, 2H, J = 10 Hz), 6.98-7.08 (m, 4H), 4.06 (m, IH), 3.89-4.00 (m, 2H), 3.35-3.50 (m, 3H), 3.1 1 (m, IH), 2.91 (m, IH), 2.76 (t, 2H, J = 8 Hz), 2.13 (s, 3H), 1.38 (d, 9H), 1.20 (d, 6H, J = 8 Hz).

A solution of the N-acetyl derivative (1.54 g, 2.46 mmol) in 30 mL of methanol with 20 mL of 2 N _. hydrochloric acid was refluxed at 90°C for 20 h. The solvent was stripped under vacuum and the residue was purified by flash column chromatography (silica gel, 90:10:1 methylene chloride/methanol /30% ammonium hydroxide) to give 970 mg (83 %) of the titled compound. 1 H NMR (400 MHz, CD3OD) δ 7.64 (d, 2H, J = 8 Hz), 7.60 (d, IH, J = 2 Hz), 7.32 (d, 2H, J = 8 Hz), 7.19 (dd, IH, J = 2,10 Hz), 7.08 (d, 2H, J = 8 Hz), 7.00 (d, 2H, J = 8 Hz), 6.56 (d, IH, J = 10 Hz), 3.98 (m, IH), 3.81-3.89 (m, 2H), 2.92 (hept, IH, J = 8 Hz), 2.65-2.86 (m, 6H), 1.21 (d, 6H, J = 8 Hz).FAB-MS mle 485 (M+l).

Following procedures outlined for Examples 185-191 , the compounds listed in Table 7 were prepared.

EXAMPLE 207

(S)-2-l(4-acetamido-3.5-dichlorophenoxy)methyl1oxirane

4- Acetamido-3 ,5-dichlorobenzenediazonium tetrafluoro- borate was converted to the corresponding phenol according to the procedure of T. Cohen, et. ah, J. Org. Chem., 42, 2053-2058 (1977). Thus, 22 g (94 mmol) of copper (II) nitrate was dissolved in 100 mL of water and 300 mg (0.94 mmol) of 4-acetamido-3,5-dichlorobenzene- diazonium tetrafluoroborate was added. Copper (I) oxide (405 mg, 2.8 mmol) was added. The mixture was stirred for 35 min, then filtered through Celite, diluted with 1 N aqueous sodium bisulfate, and extracted with 4 portions of dichloromethane and 8 portions of ethyl acetate. The combined organic phases were dried over magnesium sulfate and concentrated. Purification by flash chromatography (silica, 50% ethyl acetate/hexanes) gave 72 mg (35%) of 4-acetamido-3,5-dichlorophenol. This compound was converted to the title compound in a manner analogous to that of Example 1 : lH NMR (400 MHz, CDCI3) δ 6.97 (s, 2H), 4.21 (dd, IH), 3.86 (dd, IH), 3.32 (m, IH), 2.91 (t, IH), 2.73 (dd, lH), 2.20 (s, 3H).

EXAMPLE 208

£S)-N-l4-f2-[[2-hydroxy-3-(4-acetamido-3,5-dichloropheno xy)propyl]- aminolethvnphenyll-2-naphthalenesulfonamide

The Cbz amine from Example 13 was deprotected as described in Example 6. In a manner analogous to that of Example 7, the title compound was prepared from the resultant amine and the epoxide from Example 207: l H NMR (400 MHz, CD3OD) δ 8.28 (d, IH, J = 1.7 Hz), 7.95-7.90 (m, 3H), 7.72 (dd, IH, J = 1.9, 8.7 Hz), 7.63- 7.57 (m, 2H), 7.09-7.02 (m, 6H), 4.02 (m, IH), 3.97-3.88 (overlapping dd, 2H), 2.89-2.72 (m, 6H), 2.15 (s, 3H).

EXAMPLE 209

(S)-N-[4-[2-[[2-hydroxy-3-(4-amino-3,5-dichlorophenoxy)pr opyl]- aminolethyllphenvn-2-naphthalenesulfonamide

A solution of 28 mg (0.016 mmol) of the acetamide from Example 208 in 5 mL of methanol and 0.24 mL of 2N aqueous hydrochloric acid was heated at reflux for 3 days. It was then cooled and concentrated. Purification by HPLC (ODS-3, 1 :1 methanol:0J % aqueous trifluoroacetic acid) gave 6.7 mg (13%) the title compound as its bis trifluoracetate salt: lH NMR (400 MHz, CD3OD) δ 8.31 (d, IH,

J = 1.5 Hz), 7.96-7.90 (m, 3H), 7.75 (dd, IH, J = 1.9, 8.7 Hz), 7.65- 7.57 (m, 2H), 7.1 1 (s, 4H), 6.89 (s, 2H), 4.12 (m, IH), 3.89 (dd, IH, J =

5.0, 9.9 Hz), 3.85 (dd, IH, J = 5.3, 9.9 Hz), 3.23-3.11 (m, 4 HO, 2.90- 2.86 (m, 2H).

EXAMPLE 210

N-l4-(3-aminopropyl)phenyllbenzenesulfonamide

A mixture of 0.5g (2.17 mmol) 4-nitrophenethyl bromide and 0.134g (2.71 mmol) of sodium cyanide in dry DMSO was stirred at room temperature for 2 h. The resulting reaction mixture was diluted with water (50 mL) and extracted with methylene chloride twice. The combined organic layers were washed with water, brine, dried over magnesium sulfate and concentrated. The product was isolated by column chromatography on silica gel (15% ethyl acetate/85% Hexanes) to give 0.32 g (84 %) of the 4-nitrophenethyl nitrile.

A 0.3 g-portion (1.7 mmol) of nitro compound in methanol was hydrogenated in the presence of 300 mg of 10% Pd/C until hydrogen uptake ceased. The reaction mixture was filtered and the solvent evaporated from the filtrate. The resultant amine (clean by 1 H NMR) was directly used in the next step without any purification.

To a stirred solution of 0.23 g (1.57 mmol) of the resultant amine in methylene chloride (10 mL) at room temperature was added 0.417 g (2.35 mmol) of benzenesulfonyl choride, followed by 0.25 g (3.14 mmol) of pyridine. After 6 h, the reaction mixture was concentrated and purified on silica (2% methanol/ 98 methylene chloride) to yield 0.32 g of the sulfonamide nitrile. To a stirred mixture of 0.318 g (1.1 mmol) of sulfonamide nitrile and 0.53 g ( 2.22 mmol) of cobalt (II) chloride hexahydrate in methanol (10 mL) was added at room temperature in portions 0.42 g (1 1 mmol) of sodium borohydride (exothermic). The resulting reaction mixture (black) was stirred at room temperature for 5 h and acidified with 3N hydrochloric acid until the solution become clear. The reaction

mixture was concentrated and purified on silica (5% methanol/95 methylene chloride) to give 0.2 g of the amine. lH NMR (400 MHz, CD3OD) 7.73 (dd, 2H), 7.54 m,l H), 7.45 (m, 2H), 7.06-7.00 (AA\ BB', 4H).

EXAMPLE 21 1

(^-N-l4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino]p ropyI]- phenyllbenzenesulfonamide

Following the procedures outlined in Examples 7 and 12 the title compound is prepared from the amine from Example 210 and the epoxide from Example 2.

EXAMPLE 212

4-Nitrophenyl 2-chloroethyl ether

A solution of 1.611 g of 4-nitro sodium phenoxide (10 mmol), 2.15g (1.25 mL, 15.0 mmol) of l-bromo-2-chloroethane, and 4J5 g (30.0 mmol) of potassium carbonate in 60 mL of methylethyl ketone was refluxed in an oil bath overnight under nitrogen atmosphere. The reaction was cooled and the solid was filtered off. The filterate was evaporated under vacuum and the residue was purified by flash column chromatography (silica gel, eluant 2: 1 hexanes/ethyl acetate) to give 1.35 g (67%) of the title compound: lH NMR (200 MHz, CDCI3) δ 8.18 (d, 2H, y=9Hz), 6.95 (d, 2H, J=9Hz), 4.29 (t, 2H, 7=6Hz), 3.82 (t, 2H, 7=6Hz).

EX AMPLE 213

4-nitrophenyl 2-azidoethyl ether

A solution of 1 J2 g (5.55 mmol) of 4-nitro 2-chloroethyl ether (Example 212) and lithium azide (544 mg, 1 1.1 mmol) in 3 mL of DMF was heated at 60°C in an oil bath overnight under nitrogen atmosphere. The reaction was poured into water and extracted with ethyl acetate. The organics were washed with water and brine and dried over anhydrous magnesium sulfate and concentrated to give 1.12 g (97%) of the product: l H NMR (200 MHz, CDCI3) δ 8.18 (d, 2H, 7=9Hz), 6.96 (d, 2H, 7=9Hz), 4.21 (t, 2H, 7=5Hz), 3.63 (t, 2H, J=5Hz).

EXAMPLE 214

4-Nitrophenyl 2-aminoethyl ether

A solution of 4-nitro 2-aminoethyl ether (610 mg, 2.93 mmol) from Example 213 in 10 mL of THF/water (9:1 ) was treated with triphenyl phosphine (768 mg, 3.0 mmol) at ambient temperature. After stirring for 3 h, the solvent was removed under vacuum and the residue was purified by flash column chromatography on silica gel (eluant 1 :9 methanol/methylene chloride) to give 480 mg (95%) of the title compound: lH NMR (200 MHz, CD3OD) δ 8.18 (d, 2H, 7=9Hz), 6.96 (d, 2H, 7=9Hz), 4.13 (t, 2H, J=5.5Hz), 3.27 (t, 2H, i=5.5Hz).

EX AMPLE 215

BOCN

2-(4-Nitrophenoxy)ethylcarbamic acid 1 J -dimethylethyl ester

A solution of 480 mg (2.79 mmol) of amine from Example 214 in 20 mL of methylene chloride was treated with 610 mg (2.80 mmol) of di-tert-butyl dicarbonate. After stirring at room temperature for 40 min., the reaction mixture was concentrated and the resulting yellow solid was used for the next step without further purification: l H NMR (200 MHz, CDCI3) δ 8.15 (d, 2H, 7=9Hz), 6.90 (d, 2H, 7=9Hz), 4.94 (bs, IH, N-H), 4.05 (bt, 2H, 7=5.0Hz), 3.50 (q, 2H, 7=5.0Hz).

EXAMPLE 216

BOCNH ^'

NH.

2-(4-Aminophenoxy)ethylcarbamic acid 1 ,1 -dimethylethyl ester

A solution of 775 mg (2.75 mmol) of nitro compound from Example 215 in 20 mL of methanol with 10% palladium on carbon (150 mg) was introduced hydrogen via balloon at room temperature for 4 h. The catalyst was filtered off through Celite, and the filterate was concentrated under vacuum to give 690 mg of the title compound: 1 H NMR (200 MHz, CDCI3) δ 6.69 (d, 2H, 7=8Hz), 6.58 (d, 2H, 7=8Hz), 4.94 (bs, IH, N-H), 3.89 (bt, 2H, 7=5.0Hz), 3.40 (q, 2H, /=5.0Hz), 1.40 (s, 9H).

EXAMPLE 217

NHSO Ph

N-14-[2-[[(l,l-dimethylethoxy)carbonyl]amino]ethoxy]pheny llbenzene- sulfonamide

To a solution of 314 mg( 1.246 mmole) of t-BOC amine from Example 216 in 10 mL of methylene chloride was added pyridine (147 mg, 1.869 mmol, 1.5 eq) followed by benzenesulfonyl chloride (242 mg, 1.370 mmol, 1.1 eq) at room temperature. The reaction mixture was stirred at room temperature overnight and then partitioned between water and chloroform. The organic layer was separated and washed with IN hydrochloric acid, water and brine and then dried over anhydrous sodium sulfate. The solution was filtered, concentrated and the residue was purified by flash column chromatography (eluant 2: 1 hexanes/ethyl acetate) to give 248 mg (51 %) of the product: lH NMR (200 MHz, CDCI3) δ 8.01 (d, IH, 7=8Hz), 7.67 (d, 2H, 7=8Hz), 6.92 (d, 2H, y=9Hz), 6.72 (s, IH, N-H), 6.70 (d, 2H, J=9Hz), 4.90 (bs, IH, N-H), 3.89 (t, 2H, 7=5.0Hz), 3.40 (q, 2H, 7=5.0Hz), 1.40 (s, 9H).

EXAMPLE 218

NHSO Ph

(S)-N-[4-[2-[[2-hydroxy-3-[[4-[[(l ,l-dimethylethyl)dimethylsilyl]oxy]- phenoxylpropyllaminolethyloxylphenyllbenzenesulfonamide

A solution of 248 mg (0.632 mmol) of t-BOC amine from Example 217 in 2 mL of methylene chloride was treated with 1 mL of trifluoroacetic acid for 0.5 h and the reaction mixture was concentrated

under vacuum to give the resultant amine (256 mg, 100%) as a trifluoroacetic acid salt. To a solution of this amine in 5 mL of dry methanol was added diisopropylethylamine (90 mg, .70 mmol) followed by the epoxide from example 2 (70 mg, .25 mmol, 0.4 equiv). The reaction was heated at reflux in an oil bath under nitrogen overnight and then cooled to room temperamre and concentrated. Purification by preparative thin layer chromatography on silica (eluant 12:88 methanol/methylene chloride) gave 1 10 mg (77%) of the desired product as a white solid: l H NMR (400 MHz, CDCI3) δ 7.65 (dd, 2H, 7=8,lHz), 7.39 (t, IH, 7=7.7Hz), 7.38 (t, 2H, 7=7.7 Hz), 6.89 (d, 2H, 7=9Hz), 6.70 (s, 4H), 6.69 (d, 2H, J=9Hz), 4.20 (m, IH), 4.05 (m, 2H), 3.90 (m, 2H), 3.20-3.0 (m, 4H), 0.95 (s, 9H), 0.11 (s, 6H).

NHSO Ph

(S)-N-[4-[2-[[2-hydroxy-3-(4-hydroxyphenoxy)propyl]amino] e phenyllbenzenesulfonamide

In a manner analogous to that of Example 12, the title compound was prepared from the silyl ether from Example 218: lH NMR (200 MHz, CD3OD) δ 7.68 (d, 2H,7=8Hz), 7.53 (t, IH, J=8Hz), 7.43 (t, 2H, 7=8 Hz), 7.0 (d, 2H, 7=9Hz), 6.86 (d, 2H, 7=9Hz), 6.79 (d, 2H, 7=9Hz), 6.69 (d, 2H, 7=9Hz), 4.21 (m, IH), 3.92 (m, 2H), 3.50 (m, 2H), 3.40-3.20 (m, 4H), EI-MS: calculated for C23H26N2O6S 458; found 459 (M+l).