EP-A-0,260,744, published on March 23,1988, discloses (lH-imidazol-l-ylmethyl) substituted benzimidazoles as inhibitors of the androgen formation from C21-steroids, as inhibitors of the biosynthesis of thromboxane A2, and also having the capability to increase the excretion of ureic acid. EP-A-0,371,559, published on June 6,1990, discloses said benzimidazoles and analogous benzotriazoles as potent suppressers of the plasma elimination of endogenously or exogenously administered retinoic acid.

Retinoic acid (RA) is a key molecule in the regulation of growth and differentiation of epithelial tissues. However, RA is very rapidly metabolized by a series of enzymatic rections, which results in its deactivation. Inhibition of RA-metabolism leads to enhanced RA levels in plasma and tissue. Therefore, compound with such an inhibitory action, also called retinoic mimetic activity, have therapeutic and/or preventive potential in the field of dermatology and oncology.

The present invention is concerne with compound of formula the N-oxides, the pharmaceutically acceptable addition salts and the stereochemically isomeric forms thereof, wherein : X represents O, S or NR3 ; R 1 represents hydrogen, hydroxy, Cl 6alkyl or aryl; R2 represents hydrogen; C1-12 alkyl ; C3 7cycloalkyl; C2 galkenyl; aryl; Hetl; or C1-l2alkyl substituted with one or two substituents selected from C3 7cycloalkyl, hydroxy, Cl 4alkyloxy, cyano, amino, mono-and di (Cl 4alkyl) amino, mono-or di (arylCl_4alkyl) amino, di (arylCl_4alkyl) aminocarbonyloxy, (C1 4alkyl) (arylC1 4alkyl) amino, mono-and di (aryl) amino, (Cl 4alkyl) (di (C1 4alkyl)- aminoC 1 _4alkyl) amino, pyrrolidinyl, piperidinyl, piperazinyl optionally substituted with C1-4 alkyl, morpholinyl, perhydro-azepinyl, carboxyl,

C1-4 alkyloxycarbonyl, aminocarbonyl, mono-and di (Cl_4alkyl) aminocarbonyl, aryl, aryloxy and arylthio; or R1 and R2 taken together may form a bivalent radical of formula-R1-R2- wherein -(CH2)n-whereinnis2,3,4,5or6;R1-R2-represents R3 represents hydrogen, Het1orC1-6alkylsubstitutedwitharyloraryl, Het'; R5 represents hydrogen; hydroxy; mercapto; Cl 6alkyloxy; C1-6alkylthio ; aryloxy; arylthio; Hetl-oxy; Hetl-thio; C1-12alkyl optionally substituted with one, two or three substituents each independently selected from halo, hydroxy, mercapto, Cl 6alkyloxy, Cl 6alkylthio, aryloxy, arylthio, Het1-oxy, Het1-thio, C3-7cycloalkyl optinally substituted with carboxy,C1-6alkyloxy-alkyl, carbonyl, arylCl 6alkyloxy, arylCl 6alkylthio, aryl, het1 ; C2 8alkenyl optionally substituted with one, two or three substituents selected from halo, C3-7cycloalkyl, aryl, Hetl; C2-8alkynyl optionally substituted with halo, C3 7cycloalkyl, aryl; C3 7cycloalkyl optionally substituted with Cl 6alkyl or aryl; C5 7cycloalkenyl optionally substituted with C1-6alkyl or aryl; aryl; Het or -Alk-NR3R5 (i) or -NR3R5 (ii) wherein Alk represents C1-6alkanediyl ; and R5 represents hydrogen, Het1,(arylorHet1)C1-6alkyl,aryl, (aryl or Het1) carbonyl or (aryl or Het') C, _6alkyloxycarbonyl; aryl represents indanyl, indenyl, naphtyl, 5,6,7,8-tetrahydro-2-naphtalenyl, phenyl; said indanyl, indenyl, naphtyl or phenyl may be substituted with one, two, three, four or five substituents each independently selected from hydroxy, halo, nitro, cyano, amino, azido, mono-or di (C1-6alkyl)amino, C1-6alkylcarbonylamino, C1-6alkyl, phenyl,phenyloxy,phenylC1-6alkyloxy,polyhaloC1-6alkyl,hydrox yC1-6alkyl, pyridinylCI-6alkyloxy, Cl-6alkyloxy, fonnyl, carboxyl and Cl-6alkylcarbonyl; or two adjacent carbon atoms on said phenyl may be substituted by a single bivalent radical having the formula Cl-l2alkanediyl or polyhaloC1-12alkanediyl ; Het represents an unsaturated heterocycle selected from pyrrolyl, pyrazolyl, imidazolyl, triazolyl, tetrazolyl and pyridinyl; each of said unsaturated heterocycles may optionally be substituted with amino, mercapto, C1-6alkyl, C1-6alkylthio or aryl; and Hetl represents a monocyclic heterocycle selected from pyrrolidinyl, pyrrolyl, pyrazolyl, imidazolyl, 1,3,4-triazolyl, 1,2,4-triazolyl, tetrahydrofuranyl, furanyl, thiolanyl, thienyl, dioxolanyl, isoxazolyl, oxazolyl, isothiazolyl, thiazolyl, isoxazolidinyl, oxazolidinyl, isothiazolidinyl, thiazolidinyl, piperidinyl, pyridinyl,

piperazinyl, pyridazinyl, pyrimidinyl, pyrazinyl, 1,2,3-triazinyl, 1,2,4-triazinyl, tetrahydropyranyl, pyranyl, morpholinyl and dioxanyl; each of said monocyclic heterocycles may be optionally substituted with one or two substituents each independently selected from C1-4alkyl, hydroxy, amino, halo, aryl, arylcarbonyl or C_4alkyloxycarbonyl; or a bicyclic heterocycle selected from indolinyl, indolyl, indazolyl, benzimidazolyl, benzotriazolyl, benzofuranyl, benzothienyl, 2H-1- benzopyranyl, 3,4-dihydro-2H-1-benzopyranyl, benzthiazolyl, isoquinolinyl, quinolinyl, 3,4-dihydroquinolinyl, cinnolinyl, quinazolinyl, quinoxalinyl, chromanyl, 1,4-benzodioxinyl, 1,4-benzoxathianyl, benzodioxanyl and benzodioxolanyl; each of said bicyclic heterocycles may be substituted with one or two substituents each independently selected from C1-4alkyl, hydroxy, amino, halo, aryl, arylcarbonyl or C, _Qalkyloxycarbonyl.

As used in the foregoing definitions and hereinafter, halo is generic to fluoro, chloro, bromo and iodo; C3 7cycloalkyl is generic to cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and cycloheptyl; C5-7cycloalkenyl is generic to cyclopentenyl, cyclohexenyl and cycloheptenyl; C2 galkenyl defines straight and branch chained hydro-carbon radicals containing one double bond and having from 2 to 8 carbon atoms such as, for example, ethenyl, 1-propenyl, 2-butenyl, 2-pentenyl, 3-pentenyl, 3-methyl- 2-butenyl, 3-hexenyl, 3-heptenyl, 2-octenyl and the like; C1 4alkyl defines straight and branche chain saturated hydrocarbon radicals having from 1 to 4 carbon atoms such as, for example, methyl, ethyl, propyl, butyl, 1-methylethyl, 2-methylpropyl, 2,2-dimethylethyl and the like; C1-6alkyl is meant to include C1-4alkyl and the higher homologues thereof having 5 or 6 carbon atoms such as, for example, pentyl, 2-methylbutyl, hexyl, 2-methylpentyl and the like; C1-12alkyl is meant to include C1-6alkyl and the higher homologues thereof having from 7 to 12 carbon atoms such as, for example, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, 2-methylhexyl, 3- ethyloctyl and the like; C1-12alkanediyl defines bivalent straight and branche chain saturated hydrocarbon radicals having from 1 to 12 carbon atoms such as, for example, 1, 1-methanediyl, 1,2-ethanediyl, 1,3-propanediyl, 1,4-butanediyl, 1,5-pentanediyl, 1,6-hexanediyl, 1,2-propanediyl, 2,3-butanediyl, 1,7-heptanediyl, 1,8-octanediyl, 1,9-nonanediyl, 1,10-decanediyl, 1,11-undecanediyl, 1,12-dodecanediyl, 1,1,4,4-tetra- methylbutane-1,4-diyl and the like; polyhaloCl 6alkyl is defined as polyhalosubstituted C1-6alkyl, in particular C1-6alkyl substituted with 1 to 6 halogen atoms, more in particular difluoro-or trifluoromethyl; polyhaloCl-l2alkanediyl is defined as polyhalo- substituted C1-12alkanediyl, in particular Cl-12alkanediyl substituted with 1 to 12 halogen atoms; triazolyl is meant to include 1,2,4-triazolyl and 1,3,4-triazolyl;

tetrazolyl is meant to include lH-tetrazolyl and 2H-tetrazolyl; benzodioxanyl is meant to include 2,3-dihydro-1,4-benzodioxinyl.

The unsaturated heteroaryl group represented by Het may be attache to the remainder of the molecule of formula (I) through any ring carbon or heteroatom as appropriate.

Thus, for example, when the heteroaryl group is imidazolyl, it may be a 1-imidazolyl, 2-imidazolyl, 4-imidazolyl and 5-imidazolyl; when it is triazolyl, it may be 1,2,4-triazol-1-yl, 1,2,4-triazol-3-yl, 1,2,4-triazol-5-yl, 1,3,4-triazol-1-yl and 1,3,4- triazol-2-yl.

The pharmaceutically acceptable addition salts as mentioned hereinabove are meant to comprise the therapeutically active non-toxic base and acid addition salt forms which the compound of formula (1) are able to form. The acid addition salt form of a compound of formula (I) that occurs in its free form as a base can be obtained by treating said free base form with an appropriate acid such as an inorganic acid, for example, hydrohalic acid, e. g. hydrochloric or hydrobromic, sulfuric, nitric, phosphoric and the like acids; or an organic acid, such as, for example, acetic, hydroxyacetic, propanoic, lactic, pyruvic, oxalic, malonic, succinic, maleic, fumaric, malic, tartaric, citric, methanesulfonic, ethanesulfonic, benzenesulfonic, p-toluenesulfonic, cyclamic, salicylic, p-aminosalicylic, pamoic and the like acids.

The compound of formula (I) containing acidic protons may be converted into their therapeutically active non-toxic base, i. e. metal or amine, addition salt forms by treatment with appropriate organic and inorganic bases. Appropriate base salt forms comprise, for example, the ammonium salts, the alkali and earth alkaline metal salts, e. g. the lithium, sodium, potassium, magnesium, calcium salts and the like, salts with organic bases, e. g. the benzathine, N-methyl-D-glucamine, hydrabamine salts, and salts with amino acids such as, for example, arginine, lysine and the like.

Conversely said salt forms can be converted into the free forms by treatment with an appropriate base or acid.

The term addition salt as used hereinabove also comprises the solvates which the compound of formula (I) as well as the salts thereof, are able to form. Such solvates are for example hydrates, alcoholates and the like.

The N-oxide forms of the compound of formula (I) are meant to comprise those compound of formula (I) wherein one or several nitrogen atoms are oxidized to the

so-called N-oxide.

The term"stereochemically isomeric forms"as used hereinbefore and hereinafter defines all the possible stereoisomeric forms in which the compound of formula (I) exist. Unless otherwise mentioned or indicated, the chemical designation of compound denotes the mixture, and in particular the racemic mixture, of all possible stereochemically isomeric forms, said mixtures containing all diastereomers and enantiomers of the basic molecular structure. Stereochemically isomeric forms of the compound of formula (I) and mixtures of such forms are obviously intended to be encompassed by formula (1).

In particular, some of the compound of formula (I) and some of the intermediates hereinafter have at least one stereogenic center in their structure. This stereogenic center may be present in a R and a S configuration, said R and S notation is used in correspondance with the rules described in Pure Appl. Chem., 1976,45,11-30.

Some of the compound of formula (I) may also exist in their tautomeric forms. Such forms although not explicitly indicated in the above formula are intended to be included within the scope of the present invention. In particular, compound of formula (I) wherein R3 is hydrogen may exist in their corresponding tautomeric form.

Whenever used hereinafter, the term compound of formula (I) is meant to include also the N-oxides, the pharmaceutically acceptable addition salts and all stereoisomeric forms.

Whenever used hereinafter, K1 to R4 and Het are defined as under formula (I) unless otherwise indicated.

A special group of compound are those compound of formula (I) wherein one or more of the following restrictions apply: (a) X represents O, S, NH or N (aryl); more in particular X is O or S; (b) R 1 represents hydrogen, hydroxy or Cl 6alkyl; (c) R2 represents hydrogen; Cl-12alkyl; C3 7cycloalkyl; C2-8alkenyl ; aryl; Het; or Cl-12alkyl substituted with one or two substituents selected from hydroxy, C1 4alkyloxy, cyano, mono-and di (Cl_4alkyl) amino, mono-or di (arylCl_4alkyl)- amino, di (arylCl_4alkyl) aminocarbonyloxy, (c1-4alkyl)(arylC1-4alkyl)amino, (C1-4alkyl) (di (C1_4alkyl) aminoCl_4alkyl) amino, piperidinyl, piperazinyl optionally substituted with CI_4alkyl, morpholinyl, Cl_4alkyloxycarbonyl, aryl,

aryloxy and arylthio; or R1 and R2 taken together may form a bivalent radical of formula-R1-R2-wherein -R1-R2-represents-(CH2)n-wherein n is 2; (d) R represents hydrogen or C1-6alkyl ; more in particular R3 is hydrogen; (e) R4 represents hydrogen; Cl 6alkyloxy; aryloxy; Cl 12alkyl optionally substituted with one, two or three substituents each independently selected from halo, hydroxy, Cl 6alkyloxy, Cl 6alkylthio, aryloxy, arylthio, Hetl-thio, C3 7cycloalkyl optionally substituted with hydroxycarbonylC1-6alkyl, carboxyl, C1-6alkyloxycarbonyl, arylC1-6alkylthio, aryl, Hertz; C2 Salkenyl optionally substituted with one, two or three substituents selected from halo, C3 7cycloalkyl, aryl, Het'; C2 Salkynyl optionally substituted with aryl; C3 7cycloalkyl optionally substituted with Cl 6alkyl or aryl; C5-7cycloalkenyl ; aryl; Hertz; or or-Alk-NR3R5(i) -NR3R5(ii) wherein Alk represents C1-6alkanedyl ; and R5 represents hydrogen, C, 6alkyl, aryl, Het', arylCI-6alkyl, arylcarbonyl or arylC1-6alkyloxycarbonyl.

Aryl is suitably indenyl, naphtyl, 5,6,7,8-tetrahydro-naphtalenyl, phenyl; said indenyl, naphtyl or phenyl may be substituted with one, two, three, four or five substituents each independently selected from hydroxy, halo, nitro, amino, azido, Cl 6alkylcarbonyl- amino, phenyl,C1-6alkyloxy.polyhaloC1-6alkyl, Het is suitably imidazolyl, triazolyl and pyridinyl; each of said unsaturated heterocycles may optionally be substituted with C1-6alkyl, more in particular, Het is 1H-1-imidazolyl or 1,2,4-triazol-1-yl.

Hetl is suitably pyrrolyl, furanyl, thienyl, isoxazolyl, thiazolyl, piperidinyl, pyridinyl, piperazinyl, pyrimidinyl, pyrazinyl, morpholinyl and dioxanyl; each of said monocyclic heterocycles may be optionally substituted with one or two substituents each independently selected from C1-4alkyl, hydroxy, amino, halo, aryl, arylcarbonyl or C1-4alkyloxycarbonyl ; or indolyl, benzimidazolyl, benzotriazolyl, benzofuranyl, benzothienyl, 2H-1-benzopyranyl, 3,4-dihydro-2H-1-benzopyranyl, benzthiazolyl, isoquinolinyl, quinolinyl, quinoxalinyl, 1,4-benzodioxinyl, benzodioxanyl and benzodioxolanyl; each of said bicyclic heterocycles may be substituted with one or two substituents each independently selected from C1-4alkyl, hydroxy, amino, halo, aryl, arylcarbonyl or C1-4alkyloxycarbonyl.

Particular compound are those compound of formula (I) wherein R 2 is C1-12alkyl optionally substituted with mono-and di (Cl_4alkyl) amino, more in particular, R 2 is 3-pentyl, 2-propyl, 2- (dimethylamino)-ethyl or 2- (diethylamino)-ethyl.

Other particular compound are those compound of formula (I) wherein R4 is CI-12alkyl optionally substituted with one, two or three substituents each independently selected from halo, hydroxy, Cl 6alkyloxy, C, 6alkylthio, aryloxy, arylthio, Hetl-thio, C3 7cycloalkyl optionally substituted with hydroxycarbonylC1-6alkyl, carboxyl, Cl 6alkyloxycarbonyl, arylCl 6alkylthio, aryl, Hetl; aryl; Het1 ; or a radical of formula (ii).

Preferred compound are those compound of formula (I) wherein R3 is hydrogen; X is O and R4 is aryl or Cl 12alkyl optionally substituted with one, two or three substituents each independently selected from halo, hydroxy, Cl 6alkyloxy, Cl 6alkylthio, aryloxy, arylthio, Hetl-thio, C3 7cycloalkyl optionally substituted with hydroxycarbonylcl- 6alkyl, carboxyl, C1-6alkyloxycarbonyl, arylC1-6alkylthio, aryl, Het'; or a radical of formula (ii).

Other preferred compound are those compound of formula (I) wherein R3 is hydrogen, X is S and R4 is a radical of formula (ii).

More preferred are the compound of formula (I) wherein X is O ; Het is 1,2, 4-triazol- 1-yl ; R1 and R3 are hydrogen; R 2 is C1-6alkyl optionally substituted with dialkylamino; and R4 is C1-4alkyl optionally substituted with one, two or three substituents each independently selected from halo, hydroxy, C1-6alkyloxy, C1-6alkylthio, aryloxy, arylthio, Het-thio, C3 7cycloalkyl optionally substituted with hydroxycarbonylcl- 6alkyl, carboxyl, C1-6alkyloxycarbonyl, arylC1-6alkylthio, aryl or Hetl.

Most preferred are <BR> <BR> <BR> 4-chloro-N-[4-[2-ethyl-1-(1H-1,2,4-triazol-1-yl)butyl]phenyl ]-α-hydroxybenzeeacetamide; the N-oxides, the pharmaceutically acceptable addition salts and stereoisomeric forms thereof.

In general, the compound of formula (I) can be prepared by reacting an intermediate of formula (ici) wherein W1 is an appropriate leaving group such as, for example, a halogen, hydroxy or an alkylsulfonyloxy group, with an intermediate of formula (III) or a functional derivative thereof. For instance, a functional derivative of imidazole may be 1, 1'-carbonyldiimidazole.

Said rection may be performed in a reaction-inert solvent such as, for example, acetonitrile, dichloromethane or tetrahydrofuran, in the presence of a suitable base such as, for example, potassium carbonate. In case W1 is an hydroxy group, it may be convenient to perform the above rection in the presence of triphenylphosphine and diethyl azodicarboxylate or a functional derivative of any of said reagents, or in the presence of 1-hydroxy-lH-benzotriazole and dicyclohexylcarbodiimide.

In this and the following preparations, the rection products may be isolated from the rection medium and, if necessary, further purifie according to methodologies generally known in the art such as, for example, extraction, crystallization, distillation, trituration and chromatography.

Alternatively, compound of formula (I) may be prepared by N-alkylation of an intermediate of formula (IV) with an intermediate of formula (V) wherein W2 is an appropriate leaving group such as, for example, hydroxy, a phenoxy group or a halogen, in a reaction-inert solvent such as, for example, water, N, N- dimethylformamide, dichloromethane, 1,2-dichloroethane, chloroform, N, N- dimethylacetamide, 2-propanone, benzene or the like, and optionally in the presence of a suitable base such as, for example, triethylamine, pyridine or sodiumcarbonate.

Also functional derivatives of intermediates of formula (V) may be used such as, for example, an anhydride, e. g. glutaric anhydride, dihydro-2H-pyran-2,6 (3H)-dione, acetic acid anhydride; a cyanate; a thiocyanate; an isocyanate or an isothiocyanate. In some instances, it may be convenient to add an acid to the rection medium such as, for instance, acetic acid may be used together with a cyanate.

Compound of formula (I) wherein R4 is a HetICI-12alkyl or a radical of formula (i), said R4 being represented by R4'and said compound being represented by formula (I-a), can be prepared by reacting an intermediate of formula (VI) wherein W3 is a

suitable leaving group such as, for example, a halogen, with an intermediate of formula R4-H (VII) in a reaction-inert solvent such as, for example, acetonitrile, and in the presence of an appropriate base such as, for example, potassium carbonate. Compound of formula (I) wherein R1 is hydroxy, said compound being represented by formula (I-b), may be prepared by reacting an intermediate of formula (VIII) with Het-H (III) or a functional derivative thereof, in the presence of an appropriate reagent such as, for example, n-butyllithium, in a reaction-inert solvent such as tetrahydrofuran and diethylether, and optionally in the presence of chlorotriethylsilane.

Compound of formula (I) wherein R3 is hydrogen and R4 is attache by a nitrogen atom to the remainder of the molecule, said compound being represented by formula (I-c), may be prepared by reacting a primary or secundary amine of formula (VIT) with an intermediate of formula (IX) in a reaction-inert solvent such as, for example, acetonitrile.

Compound of formula (I) wherein R 2 is optionally substituted hydroxymethyl, being represented by formula (I-d), may be prepared by reacting an intermediate of formula (XI) with Het-H (XII) or a functional derivative thereof, in a reaction-inert solvent such as, for example N, N-dimethylformamide. optional substituent HOyoptional substituent X R3 3/ II I R4-C-N/O H-Het R'-C-N/CH-Het (XI) (XII) (I-d)

Compound of formula (I) can also be prepared by reacting an intermediate of formula (XIII) wherein W4 is a suitable leaving group such as, for example, hydroxy, with an intermediate of formula (XIV) in an appropriate solvent such as, for example, acetic acid, and in the presence of an acid such as, for example, concentrated sulfuric acid.

Compound of formula (I) wherein R2 is C1-4alkyloxyC1-12alkyl can be prepared by reacting an intermediate corresponding to a compound of formula (I) wherein R2 is LG-Cl 12alkyl wherein LG is an appropriate leaving group such as, for example, a alkylsulfonyloxy gro1p, with Cl 4alkylO~M+ wherein M+ is a suitable metal ion such as, for example Na+, in a suitable solvent such as methanol.

Compound of formula (I) wherein R2 is optionally substituted Cl 2alkyl, said RZ being represented by R2 and said compound being represented by formula (I-e), can be prepared by reducing an intermediate of formula (XV) using a suitable reducing agent such as, for example, sodiumborohydride, in a suitable solvent such as methanol. Compound of formula (I) wherein R1, R3 and R4 are hydrogen, said compound being represented by formula (I-f), can be prepared by reacting an intermediate of formula (XXIII) with formamide in the presence of an acid such as, for example, acetic acid.

The compound of formula (I) can also be converted into each other following art- known procedures of functional group transformation.

For example, compound of formula (I) wherein R3 is hydrogen may be converted to compound of formula (I) wherein R3 is other than hydrogen using art-known techniques.

Compound of formula (I) containing an aliphatic double bond may be converted to compound of formula (I) wherein said aliphatic double bond is reduced to a single bond using art-known hydrogenation techniques such as, for example, a rection with hydrogen in methanol in the presence of palladium on activated charcoal as catalyst.

Compound of formula (I) containing a carboxyl group may be esterified using art- known esterification techniques. Conversely, compound of formula (I) containing ester may be hydrolyse to compound of formula (I) containing the corresponding carboxyl moiety.

Also, compound of formula (I) containing a C1 6alkyloxycarbonyl substituent, may be transformed to compound of formula (I) wherein said substituent is reduced to hydroxymethyl using for instance, lithium aluminium hydride in tetrahydrofuran; and if desired, said hydroxymethyl substituent may be further transformed to a formyl group.

Said C1 6alkyloxycarbonyl may also be entirely removed. Analogously, other moities which may serve the purpose of protective group such as, for example, phenylmethyl, may also be removed usinez art-known techniques.

Compound of formula (I) wherein Rl is hydroxy can be converted to compound of formula (I) wherein R'is hydrogen using a suitable reagent such as stannous chloride.

Compound of formula (I) wherein R4 is a phenoxy group may be converted to the ureum derivatives thereof using art-known replacement techniques. For instance, a primary or secundary amine may be used optionally in the presence of dimethylamino- pyridine and a base such as triethylamine, and 1,4-dioxane may be used as solvent.

Compound of formula (I) wherein X is O may be converted to compound of formula (I) wherein X is S using art-known techniques such as, for example, the use of phosphorous pentasulfide in pyridine.

The compound of formula (I) may also be converted to the corresponding N-oxide forms following art-known procedures for converting a trivalent nitrogen into its N-oxide form. Said N-oxidation rection may generally be carried out by reacting the starting material of formula (I) with 3-phenyl-2- (phenylsulfonyl) oxaziridine or with an appropriate organic or inorganic peroxide. Appropriate inorganic peroxides comprise, for example, hydrogen peroxide, alkali metal or earth alkaline metal peroxides, e. g. sodium peroxide, potassium peroxide; appropriate organic peroxides may comprise

peroxy acids such as, for example, benzenecarboperoxoic acid or halo substituted benzenecarboperoxoic acid, e. g. 3-chlorobenzenecarboperoxoic acid, peroxoalkanoic acids, e. g. peroxoacetic acid, alkylhydroperoxides, e. g. t-butyl hydroperoxide. Suitable solvents are, for example, water, lower alkanols, e. g. ethanol and the like, hydro- carbons, e. g. toluene, ketones, e. g. 2-butanone, halogenated hydrocarbons, e. g. dichloromethane, and mixtures of such solvents.

Some of the compound of formula (I) and some of the intermediates in the present in- vention may contain an asymmetric carbon atom. Pure stereochemically isomeric forms of said compound and said intermediates can be obtained by the application of art-known procedures. For example, diastereoisomers can be separated by physical methods such as selective crystallization or chromatographic techniques, e. g. counter current distribution, liquid chromatography and the like methods. Enantiomers can be obtained from racemic mixtures by first converting said racemic mixtures with suitable resolving agents such as, for example, chiral acids, to mixtures of diastereomeric salts or compound; then physically separating said mixtures of diastereomeric salts or compound by, for example, selective crystallization or chromatographic techniques, e. g. liquid chromatography and the like methods; and finally converting said separated diastereomeric salts or compound into the corresponding enantiomers. Pure stereochemically isomeric forms may also be obtained from the pure stereochemically isomeric forms of the appropriate intermediates and starting materials, provided that the intervening rections occur stereospecifically.

An alternative manner of separating the enantiomeric forms of the compound of formula (I) and intermediates involves liquid chromatography, in particular liquid chromatography using a chiral stationary phase such as, for example, a Chiracel AD column.

Some of the intermediates and starting materials are known compound, may be commercially available or may be prepared according to art-known procedures.

In particular, intermediates of formula (II) wherein R1 is hydrogen and Wl is hydroxy, said intermediates being represented by formula (il-1), may be prepared by reducing a ketone of formula (VIT). The reduction may be performed in the presence of a suitable reducing agent in an appropriate reaction-inert solvent such as, for example, sodium- borohydride in methanol or lithiumaluminiumhydride in tetrahydrofuran and water. 3 2 X R3R2 reduction X R/R R4-C-N/C-- R4-C-N/CH OU (VIII) (il-1)

In some instances, it may be convenient to replace the hydroxy group in intermediates of formula (II-1) by another leaving group such as, for example, a halogen or a sulfonyl derivative, e. g. ap-toluenesulfonyloxy group or a alkylsulfonyloxy group, thus forming intermediates of formula (II-2) or (il-3). Said rection can be performed in a rection- inert solvent, such as, for example, chloroform, and in the presence of a suitable reagent such as, for example, thionylchloride or methylsulfonyl chloride. 3 2 SOC'2 X R3 =/R2 (II-1)--- R4-C-N/CH (II-2) X R3 R2 II I/ R4-C-N/CH O- (sulfonyl derivative) Cl- (sulfonyl derivative) (il-3)

Intermediates of formula (IV) may be prepared by reacting an intermediate of formula (XVI), wherein P is a protective group such as, for example, C1 4alkylcarbonyl, benzoyl or C1-4alkyloxycarbonyl, with an intermediate of formula (III), and by subsequently reacting the thus formed amide derivative with an acid such as, for example, hydrochloric acid. The preparation of the intermediate amide derivative may be performed using the same procedure as the one used for the preparation of compound of formula (I) starting from an intermediate of formula (II) and (III). R3 R2 R3 R2 P-N/C-W1 + (III) » PN4JX acid i (XVI)

Intermediates of formula (IV) wherein R3 is hydrogen, said intermediates being represented by formula (IV-1), may be prepared by reducing a nitro derivative of formula (XVII). Said reduction may be performed in the presence of a suitable reducing agent such as, for example, hydrogen, in an appropriate solvent such as, for example, methanol and in the presence of a suitable catalyst such as, for example, raney nickel. 2 2 reduction H R 0/wCHet N<RCI Het O/Ri H/Ri (XVII) (IV-1)

Intermediates of formula (VI) can be prepared by further reacting an intermediate of formula (IV) with an intermediate of formula (XVIII) wherein W3 is a suitable leaving group such as, for example, a halogen, in a reaction-inert solvent such as, for example, dichloromethane, and in the presence of a base such as, for example, sodium carbonate.

Intermediates of formula (X) may be prepared by reacting an intermediate of formula (IV-1) with a reagent of formula (XIX) in a rection inert solvent such as, for example, dichloromethane, and in the presence of a suitable base such as, for example, sodium hydroxide.

Intermediates of formula (XI) may be prepared by reductively reacting intramolecularly an intermediate of formula (XX) wherein W4 is a suitable leaving group such as, for example, a halogen in the presence of a suitable reagent such as, for example, sodium- borohydride, in a rection inert solvent such as, for example, methanol, and in the presence of a suitable base such as, for example, sodium hydroxide. W optional substituent optional substituent X R3 X R3 R4 C N/C-- R4 C N alo O (XX) (XI)

Intermediates of formula (XI) can be prepared by first dehydrating and deprotecting an intermediate of formula (XXI) wherein P is a protecting group such as, for example, C1 4alkylcarbonyl, benzoyl or C1 4alkyloxycarbonyl, using a suitable reagent such as, for example, an acid, e. g. hydrochloric acid, thus forming an intermediate of formula (XXII). Consequently, said intermediate of formula (XXII) may be further reacted with

an intermediate of formula (V) in the same manner as described for the rection between intermediates (IV) and (V).

Intermediates of formula (XXIII) can be prepared by first reacting an intermediate of formula (XXIV) with Het-H (ICI) or a functional derivative thereof, in the presence of an appropriate reagent such as, for example, n-butyllithium, in a reaction-inert solvent such as tetrahydrofuran and diethylether, and optionally in the presence of chlorotriethylsilane. The thus formed nitro derivative of formula (XXV) may then be reduced using for example a 15 % solution of TiCl3 in water as reducing agent in a suitable solvent such as, for example, tetrahydrofuran.

The compound of formula (I) suppress the plasma elimination of retinoids, such as all- trans-retinoic acid, 13-cis retinoic acid and their derivatives, resulting in more sustained plasma and tissue concentrations of retinoic acid and improved control of the differentiation and growth of various cell types. This action of the present compound is also called retinoic mimetic activity because administering a compound of formula (I) causes the same effect as if retinoids were administered. As such, the present compound can be used to control the rate of growth and differentiation of normal, preneoplastic and neoplastic cells, whether they are epithelial or mesenchymal; whether they are of ectodermal, endodermal or mesodermal origin.

The property to delay the metabolism of retinoic acid can be evidenced in various in vitro and in vivo experiments. A particular in vitro procedure is described in example C. I and tests the inhibitory activity of the compound of formula (I) on the metabolism of retinoic acid in human breast cancer cells. The compound of the present invention were also effective in suppressing induced vaginal keratinization effects in ovariectomized rats as is described in example C. 2.

In addition, the compound of formula (I) show little or no endocrinological side-

effects and they have good oral availability.

In view of the above described pharmacological properties, in particular their retinoic mimetic activity, the present compound are useful in the treatment and/or the prevention of disorders characterized by anormal proliferation and/or anormal differentiation of cells, in particular of cells of which the growth and differentiation is sensitive to the actions of retinoids. Such disorders are situated in the field of oncology, for example, head-and neck cancer, lung cancer, breast cancer, uterine cervix cancer, gastrointestinal tract cancer, skin cancer, bladder cancer and prostate cancer and similar disorders; and in the field of dermatology, for example, keratinization disorders such as rosacea, acne, psoriasis, severe psoriasis, lamellar ichthyosis, plantar warts, callosities, acanthosis nigricans, lichen planus, molluscum, melasma, corneal epithelial abrasion, geographic tongue, Fox-Fordyce disease, cutaneous metastatic melanoma and keloids, epidermolytic hyperkeratosis, Darier's disease, pityriasis rubra pilais, congenital ichthyosiform erythroderma, hyperkeratosis palmais et plantais, melasma, hyperpigmentation and similar disorders.

Further, the compound of formula (I) are useful in suppressing the metabolism of exogenously administered and of endogenously formed 10c, 25-dihydroxy-vitamin D3 (calcitriol). The inhibitory activity of the compound of formula (I) on the metabolic degradation of calcitriol may be evidenced by measuring the impact of said compound on the calcitriol degradation in human foreskin keratinocytes, pig kidney cells and human hepatoma cells. In view of their inhibitory effect on the calcitriol metabolism, the compound of formula (I) can be used in the treatment of vitamin D deficiency states. The"classic"application of vitamin D compound lies in the field of metabolic bone disorders. Calcitriol has also been described to influence the effects and/or production of interleukins. Further, calcitriol is of use in the treatment of diseases characterized by anormal cell proliferation and/or differentiation, in particular, keratinization disorders such as those described hereinabove (Bouillon et al., Endocrine Reviews, 1995,16,200-257).

In view of the above described uses of the compound of formula (I), it follows that the present invention provides a method of treating warm-blooded animals suffering from diseases which are characterized by an anormal proliferation and/or anormal differentiation of normal, preneoplastic or neoplastic cells, whether they are epithelial or mesenchymal; whether they are of ectodermal, endodermal or mesodermal origin.

Said method comprises the systemic or topical administration of a retinoic mimetic

amount of a compound of formula (I) effective in treating the above described disorders, in particular oncology disorders and keratinization disorders, optionally in the presence of an effective amount of a retinoic acid, a derivative or a stereochemically isomeric form thereof. The present invention further concerns a method of treating patients suffering from a pathological condition which may be beneficially influence by the administration of calcitriol or a prodrug thereof, in particular oncology disorders and keratinization disorders, said method consisting of administering to a patient (a) an effective amount of calcitriol or a prodrug thereof and (b) an effective amount of a compound of formula (I).

The compound of formula (I) may conveniently be used in combination with a chemotherapeutic agent, in particular an anti-neoplastic agent such as, e. g. daunorubicin, doxorubicin, vincristine, vinblastine, etoposide, taxol, taxotere, dactinomycin, mitoxantrone, mitomycin, trimetrexate and the like. The combination may be administered separately, simultaneously, concurrently or consecutively, or the combination may also be presented in the form of one pharmaceutical formulation.

Thus, the present invention also involves a pharmaceutical product comprising (a) a compound of formula (I) and (b) a chemotherapeutic agent, as a combine preparation for simultaneous, separate or sequential use in the therapeutic or prophylactic treatment of warm-blooded animals suffering from disorders characterized by anormal proliferation and/or anormal differentiation of cells. Such a product may comprise a kit comprising a container containing a pharmaceutical composition of a compound of formula (I), and another container comprising a pharmaceutical composition of the chemotherapeutic agent. The product with separate compositions of the two active ingredients has the avantage that appropriate amounts of each component, and timing and sequence of administration can be selected in function of the patient. The present invention further concerns a method of treating patients suffering from disorders characterized by anormal proliferation and/or anormal differentiation of cells, said method consisting of administering to a patient (a) an effective amount of a compound of formula (I) and (b) an effective amount of a chemotherapeutic agent.

Thus, the present invention also relates to compound of formula (I) as defined hereinabove for use as a medicine, in particular, for use in the manufacture of a medicament for the treatment of oncology disorders and keratinization disorders. The present invention further relates to compound of formula (I) as defined hereinabove in combination with a retinoic acid, a derivative or a stereochemically isomeric form thereof, or in combination with calcitriol or a prodrug thereof, or in combination with a

chemotherapeutic agent, in particular an anti-neoplastic agent, for use as a medicine.

For ease of administration, the subject compound may be formulated into various pharmaceutical forms. As appropriate compositions there may be cited all compositions usually employed for systemically or topically administering drugs. To prepare the pharmaceutical compositions of this invention, a retinoic mimetic effective amount of the particular compound, optionally in addition salt form, as the active ingredient is combine in intimate admixture with a pharmaceutically acceptable carrier, which may take a wide variety of forms depending on the form of preparation desired for administration. These pharmaceutical compositions are desirably in unitary dosage form suitable, preferably, for administration orally, rectally, percutaneously, or by parenteral injection. For example, in preparing the compositions in oral dosage form, any of the usual pharmaceutical media may be employe i, such as, for example, water, glycols, oils, alcools and the like in the case of oral liquid preparations such as suspensions, syrups, elixirs and solutions; or solid carriers such as starches, sugars, kaolin, lubricants, binders, disintegrating agents and the like in the case of powders, pills, capsules and tables. Because of their ease in administration, tablets and capsules represent the most advantageous oral dosage unit fors, in which case solid pharmaceutical carriers are obviously employed. For parenteral compositions, the carrier will usually comprise sterile water, at least in large part, though other ingredients, for example, to aid solubility, may be included. Injectable solutions, for example, may be prepared in which the carrier comprises saline solution, glucose solution or a mixture of saline and glucose solution. In the compositions suitable for percutaneous administration, the carrier optionally comprises a penetration enhancing agent and/or a suitable wettable agent, optionally combine with suitable additives of any nature in minor proportions, which additives do not cause any significant deleterious effects on the skin. Said additives may facilitate the administration to the skin and/or may be helpful for preparing the desired compositions. These compositions may be administered in various ways, e. g. as a transdermal patch, as a spot-on or as an ointment. Addition salts of compound of formula (I) due to their increased water solubility over the corresponding base form, are obviously more suitable in the preparation of aqueous compositions.

As appropriate compositions for topical application there may be cited all compositions usually employed for topically administering drugs e. g. creams, gellies, dressings, shampoos, tinctures, pastes, ointments, salves, powders and the like. Application of said compositions may be by aerosol, e. g. with a propellent such as nitrogen, carbon dioxide, a freon, or without a propellent such as a pump spray, drops, lotions, or a

semisolid such as a thickened composition which can be applied by a swab. In particular compositions, semisolid compositions such as salves, creams, gellies, ointments and the like will conveniently be used.

It is especially advantageous to formulate the aforementioned pharmaceutical composi- tions in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form as used in the specification and claims herein refers to physically discrete units suitable as unitary dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. Examples of such dosage unit forts are tablets (included scored or coated tables), capsules, pills, powder packets, wafers, injectable solutions or suspensions, teaspoonfuls, tablespoonfuls and the like, and segregated multiples thereof.

Other such compositons are preparations of the cosmetic type, such as toilet waters, packs, lotions, skin milks or milky lotions. Said preparations contain, besides the active ingredient, components usually employed in such preparations. Examples of such components are oils, fats, waxes, surfactants, humectants, thickening agents, antioxidants, viscosity stabilizers, chelating agents, buffers, preservatives, perfumes, dyestuffs, lower alkanols, and the like. If desired, further ingredients may be incorporated in the compositions, e. g. antiinflamatory agents, antibacterials, antifungals, disinfectants, vitamins, sunscreens, antibiotics, or other anti-acne agents.

The present invention also provides particular pharmaceutical or cosmetical compositions which comprise a pharmaceutically acceptable carrier, an effective amount of a compound of formula (I) and an effective amount of a retinoic acid, a derivative thereof or a stereochemically isomeric form thereof. Said retinoic acid containing compositions are particularly useful for treating acne or for retarding the effects of aging of the skin and generally improve the quality of the skin, particularly human facial skin.

Further, the invention also relates to particular pharmaceutical or cosmetical composi- tions which comprise a pharmaceutically acceptable carrier, an effective amount of a compound of formula (I) and an effective amount of calcitriol or a prodrug thereof.

The latter compositions are particularly useful in treating keratinization disorders.

The invention also relates to a product containing retinoic acid or a derivative thereof and a compound of formula (I) as a combine preparation for simultaneous, separate or

sequential use in dermatological or oncological disorders. The invention also relates to a product containing calcitriol or a prodrug thereof and a compound of formula (I) as a combine preparation for simultaneous, separate or sequential use in dermatological or oncological disorders. Such products may comprise, for example, a kit comprising a container with a suitable composition containing a compound of formula (I) and another container with a composition containing calcitriol or a retinoid Such a product may have the avantage that a physician can select on the basis of the diagnosis of the patient to be treated the appropriate amounts of each component and the sequence and timing of the administration thereof.

Those of skill in the treatment of the disorders described hereinabove could determine the effective therapeutic daily amount from the test results presented in the experimental part. An effective therapeutic daily amount would be from about 0.01 mg/kg to about 40 mg/kg body weight, more preferably from about 0.1 mg/kg to about 10 mg/kg body weight. It may be appropriate to administer the therapeutically effective dose once daily or as two, three, four or more sub-doses at appropriate intervals throughout the day. Said sub-doses may be formulated as unit dosage forms, for example, containing 0.1 mg to 500 mg of active ingredient per unit dosage form.

The exact dosage and frequency of administration depends on the particular compound of formula (I) used, the particular condition being treated, the severity of the condition being treated, the age, weight and general physical condition of the particular patient as well as other medication the patient may be taking, as is well known to those skilled in the art. Furthermore, it is evident that said effective daily amount may be lowered or increased depending on the response of the treated patient and/or depending on the evaluation of the physician prescribing the compound of the instant invention. The effective daily amount ranges mentioned hereinabove are therefore only guidelines.

The following examples are intended to illustrate the scope of the present invention.

Experimental part Of some compound of formula (I) the absolut stereochemical configuration of the stereogenic carbon atom (s) therein was not experimentally determined. In those cases the stereochemically isomeric form which was first isolated is designated as"A"and the second as"B", without further reference to the actual stereochemical configuration.

Said"A"and"B"forms of those compound of formula (I) wherein two asymmetric carbon atoms are present were separated in their pure steroechemically isomeric forms and designated as"Al"and"A2", and"B 1"and"B2", without further reference to the actual stereochemical configuration.

As used hereinafter, "THF" is defined as tetrahydrofuran,"EtOAc"is defined as ethylacetate,"DIPE"is defined as diisopropyl ether and"RT"is defined as room temperature.

A) Preparation of the intermediate compound Example A1 Methanesulfonyl chloride (0.308 mol) was added dropwise to a solution of N- [4- (I-hydroxy-2-methylpropyl) phenyl] acetamide (0.1514 mol) and triethylamine (0.308 mol) in CH2CI2 (600ml) and the mixture was stirred at 0°C for 1 hour. The solvent was evaporated, yielding 44g (100%) of ()-4- (acetylamino)-a- (1-methylethyl) benzenemethanol methanesulfonate (ester) (interm. 1).

Example A2 A mixture of (#)-N-[4-[2-methyl-1-(1H-1, 2,4-triazol-1-yl) propyl] phenyl] acetarri-ide (0.095 mol) in HCI (3N) (250ml) was stirred and heated at 60°C for 5 hours. The mixture was cooled, poured into ice, basified with concentrated NH40H and extracted with CH2Cl2. The organic layer was dried, filtered off and evaporated. The residue was crystallized from 2-propanone/(C2H5)2O and filtered off, yielding 15. 5g (75%) of (#)-4-[2-methyl-1-(1H-1, 2,4-triazol-1-yl) propyl]-benzenamine (interm. 2; mp.

117.8°C).

In a similar manner were also prepared: (A)-4-[2-ethyl-1-(1H-1, 2,4-triazol-1-yl) butyl] benzenamine (interm. 3); (B)-4-[2-ethyl-1-(1H-1, 2,4-triazol-1-yl) butyl] benzenamine (interm. 4); and ()-4- [2-ethyl-l- (IH-1,2,4-triazol-1-yl) butyl] benzenamine (interm. 5).

Example A3 1,2-Dichloroethanone (0.027 mol) was added dropwise at RT to a solution of interme diate (5) (0.0246 mol) in sodium carbonate (10%) (450ml) and CH2Cl2(600ml). The mixture was stirred for 3 hours and then extracted with CH2Cl2. The organic layer was separated, dried, filtered and the solvent was evaporated, yielding 7g (89%) of (#)-2-chloro-N-[4-[2-ethyl-1-(1H-1, 2,4-triazol-1-yl) butyl] phenyl] acetamide (interm. 6).

Example A4 a) (#)-4-(2-methyl-3-phenylpropyl) pyridine (0.114 mol) was added portionwise at 0°C to sulfonic acid (63ml), the mixture was stirred at 0°C for 1 hour and then at RT for 2 hours. The miaxture was poured into ice, basified with NH40H and the precipitate was filtered off, yielding 29.31g (100%) of ()-4- [2-methyl-l- (4-nitrophenyl) propyl]- pyridine 7).

b) Intermediate (7) (0.183 mol) in methanol (470ml), NH40H (47ml) and a solution of thiophene in methanol (4%; lml) was hydrogenated at RT with palladium on activated carbon (10%; 7.7g) as a catalyst over a 2 hour period under a 3 bar pressure in a ParT apparats. After uptake of hydrogen, the catalyst was filtered through celite and the filtrate was evaporated, yielding 42.79g of product. A sample (3g) was taken up in CH2Cl2 and purifie on a glass filter over silica gel (eluent: CH2Cl2/CH3OH 99.5/0.5). The pure fractions were collecte and evaporated. The residue was purifie further by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 97.5/2.5/0.1). The pure fractions were collecte and evaporated. The residue was recrystallized from (C2H5) 20 and filtered off, yielding 0.86g of ()-4- [2-methyl-l- (3-pyridinyl) propyl] benzenamine (interm. 8; mp. 101. 5°C).

Example A5 a) A mixture of N- [4- (2-chloro-1-oxopropyl) phenyl] acetamide (0.19 mol), N-methyl- methanamine hydrochloride (1: 1) (0.38 mol) and K2CO3 (78.8g) in CH3CN (1400ml) was stirred and refluxed for 12 hours. The mixture was cooled, poured into water and extracted with CH2Cl2. The organic layer was dried, filtered and the solvent was evaporated, yielding 39.77g (89%) of (#)-N-[4-[2-(dimethylamino)-1-oxopropyl]phenyl]- acetamide9). b) Sodium tetrahydroborate (2.6 mol) was added portionwise at 0°C under N2 flow to a mixture of intermediate (9) (2.18 mol) in methanol (5000ml). The mixture was stirred for 1 hour, poured out into ice water (5000ml) and extracted with CH2Cl2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was stirred in DIPE, filtered off and dried, yielding 357g (70%) of ()-N- [4- [I-hydroxy- 10).2-(dimethylamino)propyl]phenyl]acetamide(interm.

Example A6 Sodium tetrahydroborate (0.0502 mol) was added portionwise at 0°C to a mixture of ()-N- [4- (2-chloro-1-oxopropyl) phenyl]-3,4-dimethoxybenzeneacetamide (0.0502 mol) in methanol (280ml). The mixture was stirred at 0°C for 1 hour, then poured out into a mixture of NaOH (280ml) and ice, stirred for 1 hour and extracted with CH2Cl2. The organic layer was separated, dried, filtered and the solvent was evaporated, yielding 15.48g (94%) of ()-3, 4-dimethoxy-N- [4- (3-methyl-2-oxiranyl) phenyl] benzeneacetamide (interm.11).

Example A7 a) n-Buthyl-lithium in hexane (1.6M; 71. 6ml) was added dropwise at-70°C under N2 flow to a mixture of 1-methylmidazole (0.1146 mol) in THF (195m1). The mixture was stirred at-70°C for 30 minutes. Chlorotrietylsilane (0.1146 mol) was added. The

mixture was brought slowly to 10°C and cooled again to -70°C. n-Buthyl-lithium in hexane (1.6M; 71. 6ml) was added dropwise. The mixture was stirred at-70°C for 1 hour, brought to-15°C and cooled again to-70°C. A mixture of 4-chlorophenyl-4- nitrophenyl-methanone (0.095 mol) in THF (150ml) was added dropwise. The mixture was stirred at-70°C for 30 minutes, hydrolized and extracted with EtOAc. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2Cl2/CH3/OH/NH4OH 96/4/0.1). The desired fractions were collecte and their solvents were evaporated, yielding 6.5g (20%) of ()-a- (4-chlorophenyl)-1-methyl-a- (4-nitrophenyl)-1H-imidazole-2- methanol (interm 12), 8.7g (26.6%) of ()-a- (4-chlorophenyl)-1-methyl-a- (4-nitrophenyl)- lH-imidazole-5-methanol (interm 13) and 18g (53%) of the mixture of intermediate 12 and 13. b) A mixture of intermediate 12 and 13 (0.09 mol) in THF (600ml) was cooled on an ice bath. TiC13 in H20 (15%; 400ml) was added dropwise quickly. The mixture was stirred at RT for 90 minutes, poured out on ice, alkalized with NaOH 10N, then filtered over celite, pasted up and extracted with CHOC12. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2Cl2/CH3OH 94/6). Two pure fractions were collecte and their solvents were evaporated. Both residues were crystallized from CH3CN and DIPE. Each phe precipitate was filtered off and dried, yielding 2g (7. 1%) of ()-a- (4-aminophenyl)-a- (4-chlorophenyl)-1-methyl-1H-imidazole-2-methanol (interm. 14) and 1. 5g (5.3%) of ()-a- (4-aminophenyl)-a- (4-chlorophenyl)-1-methyl-1H- imidazole-5-methanol (interm. 15).

B) Preparation of the compound of formula (I) Example B 1 A mixture of ()-4- (acetylamino)-a- (1-methylethyl) benzenemethanol methane sulfonate (ester) (0.1541 mol), 1H-1, 2,4-triazole (0.308 mol) and K2CO3 (0.308 mol) in CH3CN (500ml) was stirred and refluxed for 12 hours. The solvent was evaporated and the residue was taken up in water/CH2/Cl2. The organic layer was dried, filtered off and the solvent evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2Cl2/CH3OH 97/3). The pure fractions were collecte and evaporated, yielding 10g (25%) of (#)-N-[4-[2-methyl-1-(1H-1, 2,4-triazol-1-yl) propyl]- phenyl] acetamide (compound 153).

Example B2 A solution of 2-methyl-3-phenyl-2-propenoyl chloride (0.0554 mol) in CH2Cl2 (50ml) was added dropwise to a solution of (#)-4-[2-methyl-1-(1H-1, 2,4-triazol-1-yl) propyl]-

benzenamine (0.037 mol) in pyridine (8ml) and CHZC12 (100m1) and the mixture was stirred at RT for 4 hours. The solvent was evaporated and the residue was taken up in water/EtOAc. The organic layer was dried, filtered and the solvent evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH99/1/0.1). The pure fractions were collecte and evaporated.

The residue was crystallized from (C2H5) 20/methylethylketone, yielding 2.7g (21 %) of ()- (E)-2-methyl-N- [4- [2-methyl-1- ( 1H-1,2,4-triazol-1-yl) propyl] phenyl]-3-phenyl-2- propenamide (compound 154).

Example B3 A mixture of 1-hydroxy-1H-benzotriazole (0.0227 mol) in THF (90mol) was added dropwise at 5°C under N2 flow to a solution of (A)-4-[2-ethyl-1-(1H-1, 2, 4-triazol-1- yl) butyl] benzenamine (0.015 mol) and ()-4-chloro-a-hydroxybenzeneacetic acid (0.0227 mol) in THF (95ml). A mixture of N, N-methanetetraylbis [cyclohexanamine] (0.0227 mol) in CH2Cl2 (37ml) was added dropwise at 5°C under N2 flow. The mixture was stirred at RT for 15 hours. The precipitate was filtered off and washed with CH2CI2. The filtrate was taken up in K2CO3 10% and extracted with CHOC12. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue (9.25g) was purifie by column chromatography over silica gel (eluent: CH2Cl2/ CH30H 96/4). The pure fractions were collecte and the solvent was evaporated, yielding 4.8g (78%) of (#)-(A)-4-chloro-N-[4-[2-ethyl-1-(1H-1, 2,4-triazol-1-yl) butyl]- phenyl]-a-hydroxybenzeneacetamide (compound 16).

Example B4 (#)-(E)-N-[4-[1-(1H-imidazol-1-yl)-2-methylpropyl]phenyl]-2- methyl-3-phenyl-2- propenamide (0.0144 mol) in methanol (200ml) was hydrogenated with palladium-on- charcoal 10% (0.52g) as a catalyst at RT over a 5 hour period under a 1 bar pressure in a Parr apparats. After uptake of hydrogen, the catalyst was filtered through celite and the solvent was evaporated. The residue was crystallized from 2-butanone/DIPE, yielding 4.9g (94%) of ()-N- [4- [1- (1H-imidazol-1-yl)-2-methylpropyl] phenyl]-a-methyl- benzenepropanamide (compound 164).

Example B5 A mixture of 4- [1- (lH-imidazol-1-yl)-2-methylpropyl] benzenamine (0.0185 mol) in formic acid (20mol) was stirred and heated at 120°C for 15 minutes. The mixture was poured into water, basified with NaOH 3N and extracted with EtOAc. The organic layer was dried, filtered off and the solvent evaporated, yielding 3.9g (86.6%) of (#)-N-[4-[1-(1H-imidazol-1-yl)-2-methylpropyl]phenyl] formamide (compound 177).

Example B6 a) A mixture of 4-[1-(1H-imidazol-1-yl)-2-methylpropyl]benzenamine (0.023 mol) and dihydro-2H-pyran-2,6 (31-dione (0.03 mol) in THF (200ml) was stirred and refluxed for 12 hours. When the rection was complete, the solvent was evaporated, yielding 7.5g(#)-5-[[4-[1-(1H-imidazol-1-yl)-2-methylpropyl[]phenyl]a mino]-5-oxopentanoicacid (compound 218). b) A mixture of (compound 218) (0.023 mol) in ethanol (200ml) and H2SO4 (3ml) was stirred and refluxed for 12 hours. When the rection was complete, the solvent was evaporated, the residue was taken up in water and extracted with CH2CI2. The organic layer was dried, filtered and the solvent evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2CI2/CH30H/NH40H 97/3/0.1).

The pure fractions were collecte and evaporated. The residue was crystallized from 2-butanone and DIPE, yielding 1.45g (18%) of (#)-ethyl 5-[[4-[1-(1H-imidazol-1-yl)-2- methylpropyl] phenyl] amino]-5-oxopentanoate (compound 219).

Example B7 A mixture of (A)-N-[4-[1-(1H-imidazol-1-yl)-2-methylpropyl]phenyl]-4-nitr obenzene- acetamide (0.0005 mol) in methanol (soma) was hydrogenated at RT (p=2 bar) for 4 hours with Raney Nickel (0.2g) as a catalyst. After uptake of hydrogen, the catalyst was filtered off over celite,"-ashed with CH30H and the solvent was evaporated. The residue (0.12g) was purifie by column chromatography over silica gel (eluent: CH2CI2/CH30H/NH40H 96. 5/3. 5/0.1). The pure fractions were collecte and the solvent was evaporated. The residue was crystallized from diethyl ether. The precipitate was filtered off and dried, yielding 0. 035g (19%) of (A)-4-amino-N- [4- [I- (lH-imidazol-1-yl)-2-methylpropyl] phenyl] benzeneacetamide (compound 145).

Example B8 A solution of NaNO2 (0.0023 mol) in water (6ml) was added at 0°C/-5°C to a solution of (B)-4-amino-N-[4-[1-[(1H-imidazol-1-yl)-2-methylpropyl]pheny l]-3-iodobenzeneacetamide (0.0021 mol) in HCI 2N (17ml). The mixture was stirred at 0°C for 15 minutes. A solution of NaN3 (0.0023 mol) in water (6ml) was added. The mixture was stirred at 0°C for 2 hours, then neutralized with K2CO3 10% and extracted with CHOC12. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/ NHtOH 97/3/0.1). The pure fractions were collecte and the solvent was evaporated.

The residue was crystallized from 2-butanone and DUPE. The precipitate was filtered off and dried, yielding 0.46g (44%) (B)-4-azido-N- [4- [1- (1H-imidazol-1-yl)-2-methyl- 259).propyl]phenyl]-3-iodobenzenacetamide(compound

Example B9 A mixture of (#)-2-chloro-N-[4-[2-ethyl-1-(1H-1, 2,4-triazol-1-yl) butyl] phenyl] acetamide (0.0218 mol), 1-methylpiperazine (0.0436 mol) and K2CO3 (0.0436 mol) in CH3CN (150ml) was stirred and refluxed for 4 hours. The mixture was cooled, poured out into water and extracted with CH2C12. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue (8.13g) was purifie by column chromato- graphy over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 96/4/0.5). The pure fractions were collecte and the solvent was evaporated. The residue was crystallized from diethyl ether. The precipitate was filtered off and dried, yieldino 3g (35.8%) (#)-N-[4-[2-ethyl-1-(1H,-1,2,4-triazol-1-yl)butyl]phenyl]-4- methyl-1-piperazineacetamide (compound 15).

Example B 10 Compound (16) (0.0116 mol) was separated into its enantiomers by column chromatography (eluent: hexane/2-propanol 50/50; column: CHIRACEL OD 20 pm).

Two pure fractions were collecte and their solvents were evaporated. The residue was crystallized from diethyl ether. The precipitate was filtered off and dried, yielding 1.77g (35%) (#)-A1-4-chloro-N-[4-[2-ethyl-1-(1H-1,2,4-triazol-1-yl)butyl ]phenyl]-α- hydroxybenzeneacetamide (compound 17) and 1.72g (4 ? %) ()- (A2)-4-chloro-N- [4- [2- ethyl)-1-(1H-1, 2,4-triazol-1-yl) butyl] phenyl]-a-hydroxybenzeneacetamide (compound 18).

Example B 11 HCI conc. (3. 6ml) was added at RT to a mixture of (#)-1,1-dimethylethyl 4-[[[4-[2-ethyl- 1-(1H-imidazol-1-yl)butyl]phenyl] amino] carbonyl]-1-piperidinecarboxylate (0.0032 mol) in EtOAc (30ml). The mixture was stirred at RT for 4 hours, then basified with a concentrated NaOH solution and extracted with EtOAc and then CH2CI2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue (1g) was converted into the hydrochloric acid salt (1: 1) in 2-propanol. The precipitate was filtered off and dried, yielding 0.85g (68%) ()-N- [4- [2-ethyl-1- (1H-imidazol-1-yl) butyl]- phenyll-4-piperidinecarboxamide monohydrochloride (compound 57).

Example B12 A mixture of a- (4-chlorophenyl)-3-pyridinemethanol (0. 364mol) and N-phenyl acetamide (0. 364mol) in HOAc (360ml) and H2SO4 36N (38. 6ml) was stirred and refluxed for 6 days. The solvent was evaporated, yielding 122.6- ()-N- [4- [ (4-chloro- phenyl) (3-pyridinyl) methyl] phenyl] acetamide (compound 673).

Example B 13 Butyllithium, 1.6M in hexane (146ml) was added dropwise at-78°C under N2 flow to a

solution of 2-bromopyridine (0.1348 mol) in THF (300ml). The mixture was stirred at -78°C for 20 minutes. A solution of N- (4-formylphenyl) acetamide (0.1226 mol) in THF (300ml) was added at -60°C/-70°C. The mixture was stirred at-60°C/-70°C for 1 hour, then poured out into ice water and extracted with EtOAc. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue (27g) was purifie by column chromatography over silica gel (eluent: CH2CI2/CH3OH/NH4OH 96/4/0.1). The pure fractions were collecte and the solvent was evaporated. The residue was crystallized from diethyl ether and 2-propanone. The precipitate was filtered off and dried, yielding 5.09g (17%) ()-N- [4- [hydroxy (2-pyridinyl) methyl]phenyl]- acetamide (compound 688).

Example B 14 To a solution of 4- [2-methyl-l- (3-pyridinyl) propyl] benzenamine (0.187 mol) into CH2CI2 (400 ml) was added dropwise A120 (100 ml). The mixture was stirred for 24 hours at RT. The mixture was hydrolyzed by H20 and neutralized by NH40H. The organic layer was washed with water and dried. The filtrate was evaporated, yielding 50 g of N-[4-[2-methyl-1-(3-pyridinyl)propyl]phenyl]acetamide (compound 671).

Example B 15 1H-1, 2,4-triazole (0.19 mol) and triphenylphosphine (0.19 mol) were added to a mixture of (#)-N-[4-[1-hydroxy-2-(dimethylamino)propyl]phenyl]acetamide (0.1269 mol) in THF (300ml.) The mixture was cooled to 0°C. Diethyl 1,2-hydrazinedicarboxylate (0.19 mol) was added dropwise. The mixture was stirred at RT overnight. The solvent was evaporated and the residue was taken up in EtOAc and Cl 1N was added. The mixture was separated into its layers. The aqueous layer was washed with EtOAc, basified with a K2CO3 solution and extracted with CH2CI2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 93/7/0.1 and 80/20/0.1). Two pure fractions were collecte and their solvents were evaporated. The desired fraction was recrystallized from 2-propanone/EtOAc. The precipitate was filtered off and dried, yielding 1.2g of (#)-(B)-N-[4-[2-(dimethylamino)-1-(1H-1, 2,4- triazol-1-yl) propyl] phenyl] acetamide (compound 631).

Example B 16 A mixture of ()- (E)-N- [4- [1- (1H-imidazol-1-yl)-2-methylpropyl) phenyl]-2- [ (4-nitrophenyl)- methylene] propanamide (0.00742 mol) in THF (80m1) and TiCl3 (30ml) was stirred at 0°C for 15 minutes. The mixture was poured into water, ice and NaOH 3N and extracted with CH2Cl2 (2x100ml)l. The combine organic layers were dried, filtered and the solvent evaporated. The residue was taken up in CH2CI2 and (C2HS) 20. The

precipitate was filtered off and stirred K2CO3 10% and CH2Cl2, dried, filtered off and evaporated. The residue was crystallized from 2-propanone. The precipitate was filtered off, taken up in Na2CO3 10% and CH2Cl2. The organic layer was dried, filtered off and evaproated. The residue was purifie by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 96/4/0.1). The pure fractions were collecte and evaporated. The residue was crystallized from (C2H5) 20, yielding 1. 5g ()- (E)-2- [(4-aminophenyl)methylene]-N-[4-[1-(1H-imidazol-1-yl)-2-meth ylpropyl]phenyl]propanamide (compound 611).

Example B 17 1, 1'-Carbonyldiimidazole (0.236 mol) was added at 60°C to a solution of ()-N- [4- [1-hydroxy-2-methylpropyl] phenyl] acetarnide (0.115 mol) in tetrahydrofuran (240ml) and the mixture was stirred at 60°C for 12 hours. The solvent was evaporated and the residue was taken up in water/CH2CI2. The organic layer was dried, filtered and the solvent evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH--'C12/CH30H 95/5). The pure fractions were collecte and evaporated. The residue was crystallized from 2-propanone, yielding 28.27g (67%) (#)-N-[4-[1-(1H- imidazol-1-yl)-2-methylpropyl] phenyl] acetamide (compound 521).

Example B 18 LiAIH4 (0.0117 mol) was added portionwise at 0°C to a solution of (#)-ethyl <BR> <BR> (A)-ß-[4-[[(3,4-dimethoxyphenyl)acetyl]amino]phenyl]-α-met hyl-1H-imidazol-1-propanoate (0.0117 mol) in THF (78ml). The mixture was allowed to warm to RT overnight and then cooled to 0°C. LiAlH4 (0.0117 mol) was added portionwise at 0°C. The mixture was allowed to warm to RT, then stirred at RT for 2 hours, poured out on ice and filtered over celite. The filtrate was extracted with EtOAc. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2C12/CH30H/NH40H 95/5/0.1 and 90/10/0.2). Two pure fractions (F1 and F2) were collecte and their solvents were evaporated. F1 was crystallized from 2-propanone. The precipitate was filtered off and dried, yielding 0.9g ()- (A)-3,4-dimethoxy-N- [4- [l- (lH-imidazol-1-yl)-2- (hydroxy- methyl) propyl] phenyl] benzeneacetamide (19%) (compound 386). F2 was purifie by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH95/5/0. 2). The pure fractions were collecte and the solvent was evaporated. The residue was purifie by column chromatography over amino phase (eluent: CH2CI2/CH3OH 95/5). The pure fractions were collecte and the solvent was evaporated, yielding 0. 5g ()- (B)-3, 4-dimethoxy-iV- [4- [l- (lH-imidazol-1-yl)-2- (hydroxymethyl) propyl] phenyl]- benzeneacetamide (10%) (compound 394).

Examnle B 19 A mixture of ()-3,4-dimethoxy-N- [4- [I- (lH-imidazol-1-yl)-2- [methyl (phenylmethyl)- amino] propyl]phenyl] benzenacetamide (0.0066 mol) in ethanol (150mol) was hydrogenated (p=3 bar) for 90 minutes with palladium-on-charcoal 10% (3.3g) as a catalyst. After uptake of hydrogen, the catalyst was filtered off over celite, washed with CH30H and the solvent was evaporated. The residue (2.72g) was purifie by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH92/8/1). Two pure fractions were collecte and their solvents were evaporated. Each residue was crystallized from 2-butanone and diethyl ether. The precipitate was filtered off and dried, yielding 0.39g (14.5%) of ()- (A)-3, 4-dimethoxy-N- [4- [1- (1H-imidazol-1-yl)-2- (methylamino) propyl] phenyl]benzeneacetamide (compound 400).

Example B20 A mixture of ()-3,4-dimethoxy-N- [4- (3-methyl-2-oxlranyl) phenyl] benzeneacetamide (0.0442 mol) and lH-imidazole (0.221 mol) in DMF (116m1) was stirred and refluxed for 6 hours. The mixture was poured out into water and extracted with EtOAc. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2CI2/CH3OH/ NH40H 96/4/0.3). The desired fraction was taken up in CH2CI2, washed with a saturated NaCI solution, dried, filtered and the solvent was evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/ NH40H 93/7/1). The pure fractions were collecte and the solvent was evaporated.

The residue was crystallized from 2-propanone. The precipitate was filtered off and dried, yielding 1.53g (9%) of ()- (B)-3, 4-dimethoxy-N- [4- [2-hydroxy-1- (1H-imidazol- 1-yl) propyl]phenyl] benzeneacetamide monohydrate (compound 402).

Example B21 A mixture of (#)-(A)-3-[4-[[3, 4-dimethoxyphenyl) acetyl] amino] phenyl]-3- (lH- imidazol-1-yl)-2-methylpropyl methanesulfonate (0.0011 mol) in NaOCH3 (lml) and methanol (5mol) was stirred at 80°C for 3 hours. The mixture was poured out on ice and extracted with CH2Cl2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue (0.56g) was purifie by column chromatography over silica gel (eluent: CH2C12/CH3OH/NH4OH 97.5/2.5/0.1). The pure fractions were collecte and the solvent was evaporated. The residue was crystallized from diethyl ether. The precipitate was filtered off and dried, yielding 0.2g (43%) of ()- (A)-3,4- dimethoxy-N- [4- [ 1- (1H-imidazol-1-yl)-3-methoxy-2-methylpropyl] phenyl] benzene- acetamide (compound 404).

Example B22 a) A mixture of compound (698) (0.0329 mol) in NaOH 3N (300ml) was stirred and refluxed for 2 hours. The mixture was cooled, poured into ice, neutralized with concentrated HCl and extracted with CH2Cl2. The organic layer was dried, filtered and the solvent evaporated, yielding 7.91g (88%) of ()-4- [I- (lH-imidazol-1-yl)-2- methylpropyllphenylthiourea (compound 699). b) An alternative rection procedure is the following: A solution of trifluoroacetic acid (0.0715 mol) in benzene (5mol) was added dropwise to a solution of 4- [I- (IH-imidazol- 1-yl)-2-methylpropyl]benzenamine (0.0511 mol) and NaSCN (0.102 mol) in benzene (70ml), the mixture was stirred at RT for 1 hour and stirred further at 60°C for 24 hours. The mixture was cooled to 30°C, and extracted with CHOC12 and K2CO3 10%.

The organic layer was washed with water, dried, filtered and the solvent evaporated.

The residue was purifie by column chromatography over silice gel (eluent : CH2Cl2/CH3OH/NH4OH95/5/0. 5 to 90/10/0.5) (35-70im) and purifie further by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 92/8/0. 5) (15-40pu). The pure fractions were collecte and evaporated. The residue was recrystallized from 2-propanone and (C2Hs) 2O and filtered off. The product was taken up in CH2CI2, CH30H and norit. The product was recrystallized from 2-propanone and (C2H5) 2O and filtered off, yielding 1.42g ()-4- [I- (IH-imidazol-1-yl)-2-methylpropyl]- phenylthiourea (10%) (compound 699).

Example B23 A mixture of compound (206) (0.0104 mol), 2-pyridinamine (0.0104 mol) and N, N- dimethyl-4-pyridinamine (0.0052 mol) in 1,4-dioxane (100 ml) was stirred and refluxed overnight. The solvent was evaporated. The residue was dissolve in CH2CI2. The organic solution was washed with a 10% aqueous K2CO3 solution, with water, dried, filtered and the solvent was evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2CI2/CH3OH/NH40H 97/3/0.1). The pure fractions were collecte and the solvent was evaporated. The residue was crystallized from 2-propanone and DIPE. The precipitate was filtered off and dried, yielding 1.10 g (34.3%)(#)-N-(2-pyridinyl)-N'-[4-[1-(1H-imidazol-1-yl)-2-met hylpropyl]phenyl]urea (compound 274).

Example B24 n-Butyllithium 1.6M in hexane (101. 5ml) was added dropwise at-70°C under N2 flow to a mixture of 1-methyl-1H-imidazole (0.162 mol) in THF (244ml). The mixture was stirred at-70°C for 30 minutes. Chlorotriethylsilane (0.162 mol) was added. The mixture was allowed to warm to RT. n-Butyllithium 1.6M in hexane (101. 5mol) was

added dropwise at -70°C. The mixture was stirred at -70°C for 1 hour and brought to- 15°C. A mixture of intermediate (9) (0.065 mol) in THF (152ml) was added dropwise at -70°C. The mixture was allowed to warm to RT, stirred overnight, then poured out into a saturated Nli4CI solution and extracted with EtOAc. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2CI2/CH3OH/NH40H 96/4/0.5 and 80/20/2). The pure fractions were collecte and the solvent was evaporated. The residue was crystallized from 2-propanone. The precipitate was filtered off and dried, yielding l. Sg () -N- [4- [2- (dimethylamino)-l-hydroxy-l- (3-methyl-3H-imidazol-4-yl)- propyl] phenyl] acetamide (compound 771).

Example B25 Benzoylchloride (0.067 mol) was added to a solution of NH4SCN (5.09g) in 2-propanone (150ml) and the mixture was stirred and refluxed for 20 minutes. A solution of 4- [1- (lH-imidazol-1-yl)-2-methylpropyl] benzenamine (0.0557 mol) in 2-propanone 9150ml) was added and the mixture was stirred and refluxed at 80°C overnight. The mixture was cooled, filtered through celite and the filtrate was evaporated. The residue was taken up in CHOC12. The organic layer was dried, filtered and the solvent evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2CI2/CH3OH/NH4OH 98/2/0.1). The pure fractions were collecte and evaporated. The residue was recrystallized from 2-propanone and DIPE, yielding(#)-N-benzoyl-N'-[4-[1-(1H-imidazol-1-yl)-2-methylpr opyl]phenyl]thiourea (compound 698).

Example B26 A mixture of compound (689) (0.0309 mol) and iodomethane (0.062 mol) in acetonitrile (100ml) was stirred at 50°C for 2 hours. The solvent was evaporated, yielding 10.9g (91%) ()-N- [4- [1-hydroxy-1- (3-pyridinium) methyl] phenyl] acetamide iodide (compound 770) Example B27 A mixture of 1- [2-ethyl-l- (4-isothiocyanatophenyl) butyl]-lH-imidazole (0.0123 mol) and 2-benzothiazolamine (0.0148 mol) in acetonitrile (80mol) was stirred and refluxed for 12 hours. The solvent was evaporated and the residue was taken up in H20 and CH2CI2. The organic layer was separated, dried, filtered and the solvent was evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH 97.5/2.5/0.1). The desired fractions were collecte and the solvent was evaporated. The residue was purifie again by column chromatography over silica gel (eluent: CH2CI2/CH3OH/NH4OH 85/15/0.1). The pure

fractions were collecte and the solvent was evaporated. The residue was crystallized from 2-butanone and DIPE. The precipitate was filtered off and dried, yielding 0.44g (9°Io) ()-N- (2-benzothiazolyl)-N- [4- [1- (1H-imidazol-1-yl)-2-ethylbutylphenyl]- thiourea (compound 705).

Example B28 A mixture of compound (651) (0.0136 mol) and phosphorous pentasulfide (0.0136 mol) in pyridine (200ml) was stirred and heated at 120°C for 12 hours. The solvent was evaporated, the residue was taken up in water, NH40H, CH2Cl2 and CH30H (10%), and the mixture was stirred at RT for 15 minutes. The organic layer was decanted off, dried, filtered and evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2CI2/CH3OH/NH4OH 97/3/0.1). The desired fractions were collecte and evaporated. The residue was recrystallized from 2-propanone and DIPE, filtered off and dried, yielding (22%) 1.15g 4-chloro-N- (4- [1- (lH-imidazol-1-yl)-2-methylpropyl] phenyl] benzenethane-thioamide (compound 764).

Example B29 A solution of methyl N'-(3-fluorophenyl)-N-[4-[1-(1H-imidazol-1-yl)-2-methylpropy l]- phenyl] carbamimidothioate (0.0094 mol) in NH3/CH30H (60ml) was stirred and heated in autoclave at 40°C for 3 days. The solvent was evaporated and the residue was purifie by column chromatography over silica gel (eluent: CH2Cl2/CH3OH/NH4OH94/6/0. 2 to 90.10/0.5). The pure fractions were collecte and evaporated. The residue was crystallized from 2-propanone and (C2H5) 20 and filtered off, yielding 0.89g (46%) N'- (3-fluorophenyl)-N- [4- [I- (lH-imidazol-1-yl)-2- methylpropyl] phenyl] guanidine (compound 744).

Example B30 A solution of KOCN (2.25g) in water was added dropwise at RT to a mixture of 4- [l- (1H-imidazol-1-yl)-2-methylpropyl]benzenamine (0.0278 mol) in acetic acid (4mol) and water (50ml) and the mixture was stirred at RT for 1 hour. The mixture was neutralized with NaOH 3N and extracted with CH2CI2 and CH30H. The organic layer was washed with water, dried, filtered and the solvent evaporated. The residue was purifie by column chromatography over silica gel (eluent: CH2CI2/CH3OH/NH4OH 96/4/0.3). The pure fractions were collecte and evaporated. The residue was recrystallized from 2-propanone, yielding 2.7g (51.4%) ()-4- [I- (IH-imidazol-1-yl)-2- methylpropyl] phenylurea (compound 266).

Example B31 4-Fluorophenylisocyanate (0.017 mol) was added to a solution of 4- [I- (lH-imidazol-l-

yl)-2-methylpropyl]benzenamine (0.014 mol) in dry THF (100ml) and the mixture was stirred and refluxed for 2 hours. The mixture was cooled, the precipitate was filtered off and recrystallized from 2-propanone and CH30H, yielding 1.6g (32%) ()-N- (4- fluorophenyl)-N'-[4-[1-(1H-imidazol-1-yl)-2-methylpropyl]phe nyl]urea (compound 740).

Example B32 CH3I (0.00814 mol) was added at RT to a mixture of compound 792 (0.00814 mol) in 2-propanone (30ml). The mixture was stirred at RT for 6 hours, poured out into H20 and a concentrated NH4OH solution and extracted with CHOC12. The organic layer was separated, dried, filtered and the solvent was evaporated, yielding 3.18g of methyl 796).[4-[(2,5-dichlorophenyl)(1H-imidazol-1-yl)methyl]phenyl ]carbamimidothioate(comp.

Example B33 Formamide (130ml) was added to a mixture of intermediate 15 (0.043 mol) in acetic acid (130ml). The mixture was stirred at 150°C for 2 hours, cooled, poured out into ice water and basified with a concentrated NH40H solution. The precipitate was filtered off, washed with H20 and taken up in CH2Cl2 and a small amount of CH30H. The organic solution was dried, filtered and the solvent was evaporated. This fraction was crystallized from CH2Cl2, CH30H and DIPE. The precipitate was filtered off and dried, yielding 2. 2g (15.1%) of ()-N- [4- [ (4-chlorophenyl) (1-methyl-1H-imidazol-5-yl) methyl]- 793).phenyl]formamide(comp.

Example B34 Compound (779) (0.0132 mol) was separated into its enantiomers by column chromatography over silica gel (eluent: hexane/C2H5OH 80/20; column: CHIRACEL OD 20 Mm). Two pure fractions were collecte and their solvents were evaporated. The residue was dissolve in 2-propanone and 2-propanol and converted into the oxalic acid salt (1: 1). The precipitate was filtered off and dried, yielding 2.55g of (A)-N-[4-[2- (1:1)ethyl-1-(1H-imidazol-1-yl)butyl]phenyl]-3-hydroxybenzen eacetamideethanedioate (comp. 780) and 2.95g of (B)-N- [4- [2-ethyl-1- (1H-imidazol-1-yl) butyl] phenyl]-3-hydroxy- benzeneacetamide ethanedioate (1: 1) (comp. 781).

Tables 1 to 20 list the compound of formula (I) which were prepared analogous to one of the above examples.

Table 1 Co. No X ; R4 ; stereochemical descriptor if Co. No X; R4 ; stereochemical descriptor if (Ex No) not racemic and/or addition salt (Ex No) not racemic and/or addition salt 1 (B1) N; CH3 33 (B2) CH; 3,4-dihydro-2H-1- benzopyran-3-yl 2 (B2) N; C (CH3) =CHC6H5 ; (E) 34 (B2) CH; 1,3-benzodioxolan-2-yl 3 (B2) N; C6H5 35 (B2) CH; 4-OC2H5-C6H4 4 (B3) N; CH (OH) (4-Cl-C6H4) 36 (B2) CH; (2,3-dihydro-1,4- benzodioxin-6-yl)-CH2 5 (B2) N; (1,3-benzodioxolan-5-yl) methyl 38 (B2) CH; (5,5,8,8-tetramethyl-5,6,7,8- tetrahydro-2-naphtalenyl)-CH2 6 (B2) N; (3,4-diOCH3) C6H3 39 (B2) CH; (CH2) 2 (4-OC2HS-C6H4) 7 (B2) N; (2,3-dihydro-1, 4-benzodioxin-6- 40 (B5) CH; H yl)methyl 8 (B3) N; (CH2) 3 (3, 4-diOCH3-C6H3) 41 (B2) CH; CH2-(4-C6H5-C6H4) 9 (B2) N; OC6H5 42 (B2) CH; CH2Cl 10 (B3) N; (CH2) 2 (3, 4-diOCH3-C6H3) 43 (B9) CH; (1-piperidinyl) methyl 11 (B3) N; CH (OH) (3,4-diCH3-C6H3) 44 (B9) CH; (4-CH3-1-piperazinyl)-CH2 12 (B2) N; CH2O(2-OCH3-C6H4) 45 (B3) CH; 2-methoxy-5-pyridinyl 13 (B3) N; (2-NH2-benzothiazol-6-yl)-CH2 46 (B3) CH; 1- (C6H5-CO)-4-piperidinyl 14 (B2) N; CH2Cl 47 (B9) CH; (4-morpholinyl)-CH2 15 (B9) N; (4-CH3-1-piperazinyl)-CH2 48 (B3) CH; (CH2) 3 (4-OC2H5-C6H4) 16 (B3) N; CH (OH) (4-Cl-C6144); (A) 49 (B3) CH; CH2O(2-OH-C6H4) 17 (B 10) N; CH (OH) (4-Cl-C6H4); (A, A) 50 (B2) CH; CH (SCH3) (C6H5) 18 (B 10) N; CH (OH) (4-Cl-C); (A, B) 51 (B3) CH; (2-OCH3-5-pyridinyl)-CH2 19 (B3) N; CH (OH) (4-Cl-C6H4) ; (B) 52 (B3) CH; (CH2) 3 (3,4-diOCH3-C6H3) 20 (B 10) N; CH (OH) (4-Cl-C6H4); (B, A) 53 (B3) CH; 1- (tert-butoxy-carbonyl)-4- piperdinyl 21 (BIO) N; CH (OH) (4-Cl-C6H4) ; (B, B) 54 (B3) CH; CH (OH) (4-Cl-C) 22 (B2) CH; phenyl 55 (B3) CH; CH2N (CH3) 2 23 (B2) CH; 2,3-dihydro-1,4-benzodioxin- 56 (B3) CH; CH (OH) (3,4-diOCH3-C6H3) 2-yl 24 (B3) CH; C (OH) (CH3) 2 57 (Bll CH; 4-piperidinyl CH;1,4-benzodioxin-2-yl58(B3)CH;(2-NH2-6-benzothiazolyl)-CH2 25(B2) Co. No X; R4; stereochemical descriptor if Co. No X; R4; stereochemical descriptor if (Ex No) not racemic and/or addition salt (Ex No) not racemic and/or addition salt 26 (B2) CH; (2,3-dihydro-1,4-benzodioxin- 59 (B3) CH; 1-methyl-4-piperidinyl 2-yl)-CH2 27 (B2) CH; 2-pyrazinyl 60 (B2) CH; OC6H5 28 (B2) CH; (1,3-benzodioxolan-5-yl)-CH2 61 (B10 CH; (CH2) 2 (4-OCZHS-C); (A) 29 (B2) CH; 3,4-dihydro-2H-l-benzopyran-62 (B10) CH; (CH2) 2 (4-OC2Hs-C6H4); (B) 2-yl 30 (B2) CH; 5,5,8,8-tetramethyl-5,6,7,8- 63 (B23 N; 2-benzothiazolyl-NH- tetrahydro-2-naphtalenyl 31 (B2) CH; 2H-1-benzopyran-3-yl 64 (B23) CH; 2-benzothiazolyl-NH- 32 (B2) CH; (CH2) 2 (3, 4-diOCH3-C6H3) 777 (B3 N; 2-benzothiazolyl 37 (B2) CH; CH20 (2-OCH3-C6H4) 778 (B3 CH; 2-benzothiazolyl; oxalic acid 1 (1:1) Table 2 Co. Ex. X (R6)n; stereochemical Co. Ex. X (Rb) n ; stereochemical No. No. deseriptor if not racemic No. No. deseriptor if not raeemic and/or addition salt and/or addition salt 65 B2 N 4-CH3 101 B2 CH 3-OC2H5 ; 4-OC2H5 66 B2 N 4-Cl 102 B2 CH 2-OCH3; 3-OCH3 67 B3 N 3-OH 103 B2 CH 4-OC6H5 68 B2 N 4-F 104 B2 CH 2-CH3 69 B3 N 4-OH 105 B2 CH 4-OCH3 70 B2 N 3-OCH3 106 B2 CH 2-CH3; 5-CH3 71 B2 N 4-OC2HS 107 B3 CH 2-OH 72 B3 N 3-OCH3; 4-OH 108 B3 CH 3-OH; 4-OCH3 73 B2 N 3-OCH3; 4-OCH3 109 B3 CH 3-OH; oxalic acid (1: 1) 74 B2 N 3-Cl ; 4-OCH3 110 B2 CH 3-O CH3 ; 4-CH3 75 B2 N 3-CI; 4-OC2H5 111 B3 CH 4-OH 76 B2 N 3-CH3; 4-OC2H5 112 B2 CH 3-CH3; 4-CH3 77 B2 N 3-CH3; 4-CH3 113 B2 CH 2-OCH3; 4-Cl 78 B3 N 3-CH3; 4-OCH3 114 B2 CH 2-OCH3; 6-OCH3 79 B3 N 3-Cl ; 4-OH 115 B2 CH 2-OCH2C6Hs; 3-OCH3 Co. Ex. X (Rb) n; stereochemical Co. Ex. X (Rb)n; stereochemical No. No. descriptor if not racemic No. No. descriptor if not racemic and/or addition salt and/or addition salt 80 B2 N 3-OCH3; 4-OCH3; 5-OCH3 116 B2 CH 3-Cl ; 4-OCH3 81 B2 N 3-CH3; 4-CH3; 5-CH3 117 B3 CH 3-Cl; 4-OH 82 B3 N 3-OC2HS; 4-OC2H5 118 B2 CH 3-Cl ; 4-OC2H5 83 B3 N 3-OCH3; 4-Cl 119 B2 CH 3-OCH3; 5-OCH3 84 B3 N 3-OCH3; 4-CH3 120 B2 CH 2-OCHZC6H5; 5-OCH3 85 B10 N 3-CH3; 4-OCH3; (A) 121 B3 CH 4- (2-pyridinylmethoxy) 86 B10 N 3-CH3; 4-OCH3; (B) 122 B2 CH 2-OCH3; 5-CH3 87 B2 CH 4-Cl 123 B2 CH 3-CH3; 4-OCH3 88 B2 CH 4-F 124 B3 CH 2-OH; 5-CH3 89 B2 CH 2-OCH3 125 B2 CH 3-CH3; 4-OC2H5 90 B2 CH 3-OCH3 126 B3 CH 2-OCH3; 4-OCH3 91 B2 CH 3-OCH3; 4-OCH3 127 B3 CH 4- (4-pyridinylmethoxy) 92 B2 CH 4-OCH (CH3) 2 128 B3 CH 3-OC2H5; 4-OCH2C6H5 93 B2 CH 4-O(CH2)2CH3 129 B3 CH 2-CH3; 4-OH 94 B2 CH 4-CH3 130 B3 CH 4- (3-pyridinylmethoxy) 95 B2 CH 4-OC2HS 779 B3 CH 3-OH 96 B2 CH 4-O (CH2) 3CH3 780 B34 CL-OH; (A); oxalic acid (1: 1) 97 B3 CH 3-OCH3; 4-OH; 781 B34 CL-OH; (B); oxalic acid (1: 1) oxalic acid (1: 1) 98 B2 CH 2-OCH3; 5-OCH3 782 B34 N 3-OCH3; 4-CH3; (A) 99 B3 CH 4-N (CH3) 2 783 B34 N 3-OCH3; 4-CH3; (B) 100 B2 CH 3-CH3 Table 3 Co. Ex. X (R6)n ; stereochemical Co. Ex. X (Rb) n; stereochemical No. No. descriptor if not racemic No. No. descriptor if not racemic and/or addition salt and/or addition salt 131 B2 N 4-Cl 142 B3 CH 3-OCH3; 4-OH 132 B2 N 4-F 143 B3 CH 3-Cl ; 4-Cl 133 B2 N 4-CH3 144 B2 CH 4-NO2; (A) 134 B3 N 4-OH 145 B7 CH 4-NH2; (A) Co. Ex. X (Rb)n ; stereochemical Co. Ex. X (Rb) n ; stereochemical No. No. descriptor if not racemic No. No. descriptor if not racemic and/or addition salt and/or addition salt 135 B2 N 4-OC2HS 146 B2 CH 4-NO2; (B) 136 B2 N 3-OCH3; 4-OCH3; 147 B7 CH 4-NH2; (B) hydrate (1: 1) 137 B3 N 3-OH 148 B3 CH 3-I ; 4-NH2 138 B3 N 3-OCH3; 4-OH 149 B3 CH 3-I ; 4-NH2; (B) 139 B2 CH 3-OCH3; 4-OCH3; 5-OCH3 150 B3 CH 3-I ; 4-NH2; (A) 140 B2 CH 3-OCH3; 4-OCH3 151 B2 CH 4-NO2 141 B3 CH 2-Cl ; 4-Cl 152 B7 CH 4-NH2 Table 4 o No X; R4 ; stereochemical descriptor zozo No X; R4; stereochemical descriptor if (Ex No) if not additionsalt(ExNo)notrqacemicand/oradditionsaltand/or 153 (B1) N; CH3 216 (B3) CH; 2-quinoxalinyl 154 (B2) N; C (CH3) =CHC6H5; (E) 17 (B2) CH; 3,4-dihydro-2H-1-benzopyran- 2-yl 155 (B2) N; CH=CHC6H5; (E) 18 (B6a) CH; (CH2) 3C (=O) OH 156 (B2) N; C (CH3) =CH (3-Cl-C6H4); (E) 19 (B6b CH; (CH2) 3C (=O) OC2H5 157 (B2) N; C (CH3) =CH (4-F-C6Fi4); (E) 20 (B2) CH; 5-bromo-2-furanyl 158 (B2) N; C (CH3) =CH (4-pyridinyl); (E) 21 (B2) CH; 3-F-C6H4 159 (B2) N; C (CH3) =CH (4-CF3-C6H4); (E) 22 (B3) CH; C (CH3) 2 [O(4-Cl-C6H4)] 160 (B2) N; CF=CHC6H5 ; (Z) 23 (B3) CH; CH2-S-C6H5 161 (B2) N; 1,3-benzodioxolan-2-yl 24 (B3) CH; (2-pyrimidinylthio) methyl 162 (B2) N; (2,3-dihydro-1,4-benzodioxin-25 (B3) CH; 5-methyl-2-pyrazinyl 2-yl)methyl 163 (B2) CH; C2H5 26 (B2) CH; 3-methyl-2-furanyl 164 (B4) CH; CH (CH3)-CH2 (C6H5) 27 (B3) CH; 4-quinolinyl 165 (B2) CH; CH (CH3)-CH=CHC6H5; (E) 28 (B3) CH; 1,2-dihydro-2 (1H)-pyridinone- 3-yl 166 (B2) CH; C6H5 29 (B3) CH; 1-isoquinolinyl 167 (B2) CH; 2-benzofuranyl 30 (B2) CH; 2,3-dihydro-1,4-benzodioxin- S-yl X;R4;stereochemicaldescriptorConoX;R4;stereochemicaldescript orifoNo (Ex No) if not racemic and/or addition salt Ex No) not racemic and/or addition salt 168 (B2) CH; 2-benzothienyl 31 (B2) CH; 3, 4-(OCH3) 2-C6H3 169 (B2) CH; 2-furanyl 32 (B2) CH; 1,3-benzodioxolan-5-yl 170 (B2) CH; 2-pyrazinyl 33 (B3) CH; 5-quinoxalinyl 171 (B2) CH; C (CH3) =C (C6H5) 34 (B2) CH; 1,4-benzodioxin-2-yl (3-pyridinyl); (E+Z) 172 (B2) CH; 3-furanyl 35 (B2) CH; 2-furanylmethyl 173 (B2) CH; 3-thienyl 36 (B3) CH; C (OH) (CH3) 2 174 (B2) CH; 1-cyclohexenyl 37 (B2) CH; (2,3-dihydro-1,4-benzodioxin- 2-yl)methyl 175 (B2) CH; 2,3-dihydro-1,4-benzo- 38 (B2) CH; 4-(C6H5)-C6H4 dioxin-2-yl 176 (B2) CH; C (CH3) =C (C6H5) (CH3); (E) 39 (B3) CH; (4-pyridinylthio) methyl 177 (B5) CH; H 40 (B3) CH; (2-naphtalenyl) methyl 178 (B2) CH; 2-indolyl 41 (B3) CH; 3-quinolinyl 179 (B2) CH; 2-naphtalenyl 42 (B3) CH; 3,5-dimethyl-4-isoxazolyl 180 (B2) CH; 1-methyl-2-indenyl 243 (B2) CH; 2,3-dihydro-1.4-benzoxathiin- 2-yl 181 (B2) CH; 2-oxolanyl 44 (B3) CH; 2-thienylmethyl 182 (B2) CH; 1-naphtalenyl 245 (B3) CH; 3-thienylmethyl 183 (B2) CH; OC2H5 46 (B3) CH; 1-naphtalenylmethyl 184 (B2) CH; l-methylbenzotriazol-6-yl 47 (B3) CH; 2-pyridinylmethyl 185 (B2) CH; 3-oxolanyl 48 (B2) CH; 1,3-benzodioxolan-2-yl 186 (B2) CH; 2-phenyl-4-thiazolyl 49 (B3) CH; CH (OH)-CH3 187 (B2) CH; 2-thienyl 50 (B3) CH; 5-methyl-3-phenyl-4-isoxazolyl 188 (B2) CH; (CH2)2CH2Cl 251 (B3) CH; 3-pyridinylmethyl 189 (B2) CH; C (CH3) (C6H5) z 52 (B2) CH; 5,6,7,8-tetrahydro-5,5,8,8- tetramethyl-2-naphtalenyl 190 (B2) CH; 1-C6H5-cyclopropyl 253 (B2) CH; 3,4-dihydro-2H-1-benzopyran- 3-yl 191 (B2) CH; 1-C6H5-cyclopentyl 254 (B2) CH; 2H-1-benzopyran-3-yl 192 (B2) CH; cyclopentyl 55 (B2) CH; (2,3-dihydro-1,4-benzodioxin- 6-yl)methyl 193 (B2) CH; cyclohexyl 56 (B2) CH; (5,6,7,8-tetrahydro-5,5,8,8- tetramethyl-2-naphtalenyl)methyl 194 (B3) CH; 4-pyridinyl 57 (B1) CH; CH3; (A) X;R4;stereochrmicaldescriptorCoNoX;R4;stereochemicaldescript orifoNo Ex No) if not racemic and/or addition salt Ex No) not racemic and/or addition salt 195 (B3) CH; 1-methyl-2-pyrrolyl 258 (B1) CH; CH3; (B) 196 (B3) CH; 3-pyridinyl 259 (B8) CH; CH2 (3-iodo-4-azido-C6H3); (B) 197 (B2) CH; 2-methylcyclopropyl 260 (B8) CH; CH2 (3-iodo-4-azido-C6H3); (A) 198 (B3) CH; C-C (C6H^) 261 (B3) CH; CH2-NH-C(=O)-C6H5 199 (B3) CH; cyclopropyl 262 (B3) CH; CH2-NH-C(=O)-O-CH2-C6H5 200 (B2) CH; 1-C6H^-cyclohexyl 263 (B23 CH; N (CH3)-CH2-C6H5 201 (B2) CH; 1-methylcyclohexyl 64 (B6a) H; CH2-[1-(CH2COOH)cyclopentyl 202 (B2) CH; 2-methylcyclohexyl 265 (B6a) CH; (CH2)2-C (=O)-OH 203 (B3) CH; C (CH3) =C (C6Hs)-C2Hs; (Z) 66 (B30 CH; NH2 204 (B2) CH; 2-phenylcyclopropyl; 67(B23 CH; NH-CH3 oxalic acid (1: 1) 205 (B2) CH; 3,4-dihydro-2(1H)- 268 (B23 CH; NH-C (CH3) 2 quinolinone-6-yl CH;OC6H5269(B23)CH;NH-CH2-C6H506(B2) 707 (B3) CH; C (CH3) =C (C6H5) (2- 70 (B23 CH; NH- (3-pyridinyl) furanyl);(E) 708 (B3) CH; 2-pyridinyl 71(B23 CH; NH- (2-pyrazinyl) 709 (B2) CH; CH (CH3) CH ; 72 (B31 CH; NH- (I-naphtalenyl) 210 (B3) CH; CH2-S-CH2C6Hs 273 (B23 CH; NH-CH2-(4-Cl-C6H4) 211 (B3) CH; CH2-OC6Hs 274 (B23 CH; NH- (2-pyridinyl) 12 (B3) CH; CH2-OCH3 275 (B23 CH; NH- (4-pyridinyl) 13 (B3) CH; CH2-NH-C6Hs 776 (B23 CH; NH- (6-benzodioxanyl) 14 (B3) CH; 6-quinoxalinyl 277 (B23 CH; NH-(1-CH3-2-benzimidazolyl) 15 (B3) CH; 2-quinolinyl Table 5 Co. Ex. X (Rb) "; stereochemical Co. Ex. X (R6)n ; stereochemical No. No. descriptor if not racemic No. No. descriptor if not racemic and/or addition salt and/or addition salt 278 B2 N 3-OCH3; 4-OCH3; (A) 301 B3 CH 3-OC2Hs; 4-OC2Hs; (B) Co. Ex. stereochemicalCo.Ex.X(Rb)n;stereochemical(Rb)n; No. No. descriptor if not racemic No. No. descriptor if not racemic and/or addition salt and/or addition salt 279 B3 N 3-Cl ; 4-OCH3; (A) 302 B3 CH 3,4, 5-(OCH3) 3; (A) 280 B3 N 3-CH3; 4-CH3; (B) 303 B3 CH 3-Cl; 4-OH; (A) 281 B3 N 4-OCH3; 3-CH3; (B) 304 B2 CH 3-Cl ; 4-OCH3; (A) 282 B3 N 3-CH3; 4-CH3; (A) 305 B3 CH 3-CI; 4-OCH3; (B) 283 B3 N 4-Cl ; (B) 306 B3 CH 3-CH3; 4-CH3; (B) 284 B3 N 3-Cl ; 4-OH; (A) 307 B3 CH 3-Cl ; 4-OH; (B) 285 B3 N 3-OC2HS; 4-OC2H5; (A) 308 B3 CH 3-CH3; 4-CH3; 5-CH3; (A) 286 B3 N 3-CH3; 4-OCH3; (A) 309 B3 CH 3-CH3; 4-CH3; 5-CH3; (B) 287 B3 N 3-OCH3; 4-OCH3; (B) 310 B3 CH 3-OCH3; 4-Cl ; (A) 288 B3 N 3-Cl ; 4-OCH3; (B) 311 B3 CH 3-OCH3; 4-Cl ; (B) 289 B3 N 3-Cl ; 4-OH; (B) 312 B3 CH 3-CH3; 4-OCH3; (A) 290 B3 N 3-CH3; 4-CH3; 5-CH3; (A) 313 B3 CH 3-chu 4-OCH3; (B) 291 B3 N 3-CH3; 4-CH3; 5-CH3; (B) 314 B3 CH 3-OCH3; 4-CH3; (A) 292 B3 N 3,4, 5-(OCH3) 3; (B) 315 B3 CH 3-OCH3; 4-CH3; (B) 293 B3 N 3-OC2H5; 4-OC2H5; (B) 316 B3 CH 4-OCH (CH3) 2; (B) 294 B3 N ;3-OCH3 4-CH3; (A) 317 B3 CH 4-N (CH3) 2; (A) 295 B3 N ;3-OCH3 4-CH3; (B) 318 B3 CH 3-OCH3; 4-OCH3; (A) 296 B3 N ;3-OCH3 4-Cl ; (A) 319 B3 CH 4-O (CH2) 3CH3; (A) 297 B3 N ;3-OCH3 4-Cl ; (B) 320 B3 CH 4-O (CH2) 3CH3; (B) 298 B10 N 3-Cl ; 4-OH; (A, A) 321 B3 CH 4-OCH (CH3) 2; (A) 299 B10 N 3-cul; 4-OH; (A, B) 784 B34 N 4-Cl ; (B, A) 300 B3 CH 3-OC2H5 ; 4-OC2Hs; (A) 1785 B34 N 4-Cl ; (B, B) Table 6 o No X; R4 ; stereochemical descriptor Co No X; R4; stereochemical descriptor if Ex No) if not racemic and/or addition salt (Ex No) not racemic and/or addition salt @22 (B3) N; (2,3-dihydro-1,4-benzodiozin-339 (B3) CH; (2,3-dihydro-1,4-benzodioxin- 6-yl) methyl; (A) 6-yl) methyl; (B) 323 (B2) N; OC6H5; (A) 40 (B2) CH; (1,3-benzodioxolan-5-yl) methyl; (A) 24 (B2) N; 3,4-diOCH3-C6H3; (A) 341 (B3) CH; 3,4-diOCH3-C6H3; (A) o No X; R4 ; stereochemical descriptor o No X; R4 ; stereochemical descriptor if Ex No) if not racemic and/or addition salt Ex No) not racemic and/or addition salt 25 (B2) N; (1,3-benzodioxolan-5-yl)-42 (B3) CH; 3,4-diOCH3-C6H3; (B) methyl;(A) 26 (B3) N; (CH2) 3 (3,4-diOCH3-C6H3); (A) 43 (B2) CH; OC6H5; (A) 27 (B3) N; 3,4-diOCH3-C6H3; (B) 44 (B2) CH; OC6H5 328 (B3) N; (CH2) 2 (3,4-diOCH3-C6H3); (B) 45 (B5) CH; H; (A) 29 (B3) N; (CH2) 3 (3,4-diOCH3-C6H3); (B) 46 (B3) CH; (CH2) 2 (4-OC2H5-C6H4) ; (A) 330 (B3) ; (1,3-benzodioxolan-5- 47 (B9) CH; 4-methylpiperazinyl; (A) yl) methyl; (B) 331 (B5) N; H; (B) 48 (B3) CH; (CH2) 2 (4-OC2H5-C6H4) 332 (B3) N; C (CH3) =CH (C6H5); [B-(E)] 349 (B9) CH; 4-methylpiperazinyl; (B) 333 (B3) N; (2,3-dihydro-1,4-benzodioxin- 50 (B3) CH; CH [O(2-OCH3-C6H4) ; (A) 6-yl) methyl; (B) 34 (B2) N; OC6H5 ; (B) 351 (B3) CH; CH [O(2-OCH3-C6H4)]; (B) 335 (B5) N, H; (A) 52 (B3) CH; (4-CH3-piperazinyl) methyl; (A) 36 (B3) H; (CH2) 3 (3,4-diOCH3-C6H3); (B) 53 (B3) CH; (4-CH3-piperazinyl) methyl; (B) 337 (B3) CH; (1, 3-benzodioxolan-5-yl)- 354 (B3) CH; (4-CH3-piperazinyl) ethyl methyl; (B) 338 (B3) CH; (2,3-dihydro-1,4-benzodioxin- 6-yl)methyl;(A) Table 7 o No Rl; stereochemical descriptor if go No R1; stereochemical descriptor if not Ex No) not racemic and/or addition salt (Ex No) racemic and/or addition salt 355 (B2) (CH2) 2CH (CH3) 2 67 (B2) CH [N (CH3) 2] CH3; (A) 356 (B3) 4-CI-C6H4 p68 (B2) CH [N (CH3) 2] CH3; (B) 357 (B2) C6H5 69 (B2) CH (S-C6H5) CH3; (B) 358 (B2) CH3 70 (B2) CH (O-C6H5) CH3; (A) 359 (B2) CH2CH (CH3) 2 1371 (B2) CH (CH3) CH2CN; (A+B) 60 (B2) CH2-C (CH3) 3 72 (B2) C2H5 61 (B2) 3-CF3-C6H4 73 (B2) 5,6,7,8-tetrahydro-5,5,8,8- tetramethyl-2-naphtalenyl o No R 1; stereochemical descriptor if o No R1; stereochemical descriptor if not Ex No) not racemic and/or addition salt Ex No) racemic and/or addition salt 362 (B2) cyclohexyl 374 (B2) CH (CH3)C3H7 ; (B) 63 (B2) (B2)CH2[N(CH3)2]375 64 (B2) CH (CH3)CH2CH3 376 (B2) CH (S-C6H5) CH3; (A) 365 (B2) C (CH3)3 337 (B2) CH (CH3) CH2C6H5 1-(1-piperidinyl)ethyl;(A)66(B3) Table 8 0 No Rl; stereochemical descriptor if Co No Rl; stereochemical descriptor if not Ex No) not racemic and/or addition salt (Ex No) racemic and/or addition salt 378 (B2) CH (C3H7) 2 399 (B3) CH [N (CH3)(CH2C6H5)]CH3 379 (B3) CH (CH3) [N (CH3)2] ; (B) 400 (19) CH [NH (CH3) ] CH3; (A) 380 (B3) CH2 [N (CH3) 2] 401(B19) CH [NH (CH3)] CH3; (B); hydrate (1: 1) 381 (B3) CH [C (=O) OC2H5]CH3 ; (A) 402 (B20) CH (OH) CH3; (B); hydrate (1: 1) 382 (B3) CH [C (=O) OC2H5]CH3 ; (B) 403 (B18) (CH2)2 (OH) 383 (B3) CH[N(C2H5) 2] CH3; (B) 404 (B21) CH (CH3) CH2OCH3 ; (A) 384 (B3) CH (CH3)C5H11 ; (A) 405 (B21) CH (CH3)CH2OCH3 ; (B) 385 (B3) CH (CH3) C5HlI ; (B) 406 (B3) CH [N (CH3) (C4H9)] CH3; (A) (A)407(B3)CH[N(CH3)[(CH2)2N(CH3)2]]CH3;(A)86(B18)CH(CH3)CH2O H; 87 (B3) CH [N (C2H5) 2] CH3; (A) 408 (B3) 1-(4-morpholinyl) ethyl; (A) 88 (B3) CH [N (CH3) 2] C2H5; (B) 409 (B3) 1-(4-morpholinyl) ethyl; (B) 89 (B3) [1-CH3-2-(1-piperidinyl)]C2H5 ; (B) 410 (B3) 1-methyl-3-piperidinyl; (A) 390 (B3) [1-CH3-2- (I-piperidinyl)] C2H5; (A) 411 (B3) 1-methyl-2-piperidinyl; (A) 91 (B3) CH (CH3) [CH2 [N (CH3)2]] ; (B) 412 (B3) 1- (4-methyl-1-piperazinyl) ethyl; ;(A) hydrate (1: 1) 392 (B3) CH (CH3) [CH2 [N (CH3)2]] ; (A) 413 (B3) CH[N(CH3)(C3H7)]CH3 ; (A) (A)414(B3)CH[N(CH3)(C3H7)CH3;(B)93(B3)[1-N(CH3)2]C3H7; (B)415(B3)CH[N(CH3)[(CH2)2C6H5]]CH394(B18)(1-CH3)C2H5OH; 95 (B3) CH2C (=O) OC2H5 416 (B3) CH[N(CH3)(C2H5)]CH3 ; (A) 396 (B3) CH [N (CH3)(CH2C6H5)]CH3 ; (B) 417 (B3) CH [OC (=O) N (CH2C6H5) 2] CH3; (A) 97(B17) CH2OCH3 418 (B3) CH [N (CH2C6H5) 2]CH3; (B) 98 (B3) CH [N (CH3) (CH2C6H^)] CH3; (A) 419 (B3) CH [N (CH2C6H5)2]CH3 ; (A) Table 9 Co. Ex. X R1 R3 R4; stereochemical descriptor if not No. No. races-tic and/or addition salt 420 B 3 CH C6H5 H CH (OI-nC6H5 421 B2 H CH (CH3) 2 CH3 C (CH3) =CHC6H5: (E) 422 B2 H CH (CH3) 2 C2H5 C (CH3) =CHC6H5; (E) 423 B3 H 4-Cl-C6H4 H CH (OH) C6H5 424 B2 CH C6H5 H 2-pyrazinyl 425 B2 CH C6H5 H 2, 3-dihydro-1, 4-benzodioxin-2-yl 426 B2-H C6HS H (2,3-dihydro-1,4-benzodioxin-2-yl)- methyl 427 B2 CH CH (C2H5) 2 CH3 CH2 (3,4-diOCH3-C6H3) 428 B 3 CH CH [N (CH3) 2] CH3 H CH2 (3,4.5-triOCH «-C6H2); (B) 429 B3 H CH [N (CH3) 2] CH3 H (CH2) 2 (3, 4-diOCH;-C6H ;); (B) 430 B3 CH CH [N (CH3) 2] CH3 H (CH2) 2 (3, 4-diOCH.-C6H); (A) 431 B3 H CH [N (CH3) 2] CH3 H (CH2) 3 (3, 4-diOCH ;-C6H ;); (A); oxalic acid (1: 1) 432 B3 H 2-butyl H CH2 (3-OCH3-4-OH-C6H «) 433 B3 H CH2 [N (CH3) 2] H CH2 (3,4-diCH3-C6H3) 434 B3 CH CH2 [N (CH3) 2] H 3,4-diOCH3-C6H * 435 B2 CH CH2 [N (CH3) 2] H OC6H5 436 CH2[N(CH3)2]H4-methyl-l-pieprazinylCH 437 B2 N CH (CH3) [N (CH3) 2[ CH3 CH2 (3,4-diOCH3-C6H3); (B) 438 B2 N CH (CH3) [N (CH3) 21 CH3 CH2 (3,4-diOCH3-C6H3); (A) 439 B2 CH CH (CH3) [N (CH3) 2] CH3 CH2 (3,4-diOCH3-C6H3); (A) Table 10 o No RI; R6; stereochemical descriptor cl No R1; R6; stereochemical descriptor if Ex No) if not racemic and/or addition salt Ex No) not racemic and/or addition salt 440 (B2) 4-Cl-C6H4 ; H 72 (B3) CH (CH3) 2; cyclopentyl; (E) 41 (B2) 3-Cl-C6H4 ; H 73 (B3) CH (CH3) 2; cyclohexyl; (E) 442 (B2) 3-F-C6H4; H 74 (B2) CH2CH (CH3) 2; CH3; (E) 443 (B2) 4-F-C6H4 ; H 75 (B2) (CH2) 2CH (CH3) 2; CH3; (E) 44 (B2) C6H5; C6H5 76 (B2) CH2C (CH3) 3; CH3; (E); hydrate (2: 1) 45 (B2) C6H5; CH3 477 (B2) 1,3-dioxan-5-yl; CH3; (E) 446 (B2) 4-F-C6H4 ; CH3 78 (B2) CH (C2H5)2 ; CH3; (E) 447 (B2) 4-Cl-C6H4 ; C6H5 79 (B2) CH=CH-CH (CH3) 2; CH3; (E, E) 48 (B2) 3-Cl-C6H4 ; CH3 80 (B2) CH (CH3) C2H5; CH3; (E) 3-Cl-C6H4;C6H5481(B2)C(CH3)3;CH3;(E)49(B2) 450 (B2) 4-F-C6H4; C6H5 482 (B2) CH (CH3) C3H7; CH3; [A- (E)] 51 (B2) 4-Cl-C6H4 ; CH3 83 (B2) CH (S-C6H5) CH3; CH3; (A) 452 (B2) C6H5; C2H5 484 (B2) CH (S-C6H5) CH3; CH3; (B) C6H5;C3H7485(B2)CH(C6H5)2;CH3;(E)53(B2) 54 (B2) CH (CH3) 2; C6H5 486 (B2) CH (C3H7) 2; CH3 ; (E) 55 (B2) CH (CH3) 2; CH3; (E) 87 (B2) CH (CH3) C5HI, ; CH3; [A- (E)] 56 (B2) CH (CH3) 2; 2-CH3-C6H4 88 (B2) CH (CH3) C5HI; CH3; [B-(E)] 457 (B2) CH (CH3) 2; C2H5 489 (B2) CH (C6H5) CH3; CH3; [A-(E)] 58(B10 CH (CH3) 2; CH3; (+)- [A- (E)] 90 (B2) CH (C6H5) CH3; CH3; [B-(E)] 59(B10 CH (CH3) 2; CH3; (-)-[B-(E)] 491 (B2) 5,5,8,8-tetramethyl-5,6,7,8- tetrahydro-2-naphtalenyl; CH3; (E) 460 (B2) C2H5; CH3; (E) 92 (B2) CH (C2H5) C5HlI; CH3; [A- (E)] 61 (B2) CH (CH3) 2; F; (E) 93 (B2) CH (C2H5)C4H9 ; CH3; (E) 62 (B2) 9E)494(B2)CH(C2H5)C5H11;CH3;[B-(E)]CH3; 63 (B2) cyclohexyl; CH3; (E) 95 (B2) CH [N (CH3) 2] CH3; CH3; [A- (E)] 64 (B2) CH (CH3) 2; C3H7; (E) 96 (B3) CH [N (CH3) 2]CH3 ; CH3; [B-(E)] 65 (B2) CH (CH3) 2; C4H9; (E) 97 (B2) C6H5; H 466 (B2) CH3; CH3; (E) 98 (B2) H; H 67 (B2) C3H7; CH3; (E) 99 (B2) CH (CH3) 2; H 68 (B2) cyclohexyl; C6H5; (E) 00 (B2) 4-Br-C6H4 ; H 69 (B2) cyclopropyl; CH3; (E) O1 (B2) 4-CH3-C6H4; H 470 (B2) cyclopentyl ; CH3; (E) 02 (B2) CH (CH3) 2; H; (E) 71 (B3) CH (CH3) 2; CH (CH3) 2; (E) 86 (B3) 2, 5-diCl-C6H5 ; CH3; (E) Table 11 o No Rl; R6; R'; stereochemical Co No Rl; R6; R7; stereochemical Ex No) descriptor if not racemic and/or tEx No) descriptor if not racemic and/or addition salt addition salt 03 (B2) C6H5; H; C6H5 12 (B2) 4-Cl-C6H4 ; H; CH3 504 (B2) 4-Cl-C6H4 ; H; C6H5 13 (B3) 4-Cl-C6H4 ; H; C4H9 OS (B2) 3-Cl-C6H4 ; H; C6H5 514 (B3) 4-Cl-C6H4 ; H; cyclohexyl; (E+Z) 506 (B2) 4-F-C6H4 ; H; C6H5 15 (B3) 4-Cl-C6H4; H; CH (CH3) 2; (E+Z) 507 (B2) -4-Cl-C6H4 ; H; C2H5 516 (B2) 4-CI-C6H4; H; 3-pyridinyl 508 (B2) 4-F-C6H4; H; CH3 17 (B2) 4-F-C6H4; H; 3-pyridinyl 509 (B2) H; H; C6H5 518 (B3) CH (CH3) 2; CH3; 3-thienyl; (E+Z) 10 (B2) CH3; H; C6H5 519 (B3) CH (CH3) 2; CH3; C3H7; (E+Z) CH(CH3)2;H;C6H5520(B3)4-Cl-C6H4;H;3,5-diCl-C6H311(B2) Table 12 o No R'; stereochemical descriptor if Co No R1; stereochemical descriptor if Ex No) not racemic and/or addition salt (Ex No) not racemic and/or addition salt 521 (B 17 CH (CH3) 2 548 (B 1) CH2N (CH3) 2 22 (B 1) 3-Cl-CH4 549 (B1) CH (C2H5) (n-C4Hg) 23 (B 1) 3-F-C6H4 550 (B 17) 1-(ethoxycarbonyl) ethyl 24 (B1) 3-CF3-C6H4 551 (Bl) CHfN (CH3) 2] CH3; (A); hydrate (1: 1) 525 (B1) cyclohexyl 552 (B1) CH [N (CH3) Z) CH3; (B) 553(B1)CH(CH3)[CH2(C6H4)]26(B17)cyclopropyl 27 (B 17 cyclopentyl 554 (B 1) CH [N (C2H5) 2] CH3; (A) 28 (B 17 (CHz) ZCH (CH3) 2 555 (B1) CH [N (CZHS) ZCH3; (B) 529 (B 17 CH2C (CH3) 3 556 (B 1) CH [N (C2H5)2[CH3 530 (B17 1, 3-dioxan-5-yl 557 (B1) CH [N (CH3) 2] C2H5; (A) 531 (B1) CH (C2H5) 2 558 (B1) CH [N (CH3) 2]C2H5 ; (B) o No R 1 ; stereochemical descriptor if Co No R 1; stereochemical descriptor if Ex No) not racemic and/or addition salt (Ex No) not racemic and/or addition salt 532 (B 17 CH=CH-CH (CH3) 2 559 (B1) CH [N (CH3) 2] C2H5 533 (B 1) CH (CH3) C2H5 560 (B 1) (ethoxycarbonyl) methyl 34 (B1) C (CH3) 3 561 (B17) CH [N (CH3) (CH2-C6H5)] CH3 535 (B1) CH [N (CH3) 2] CH3; hydrate (1: l) 562 (B1) CH [N (CH3) (n-C4Hg)] CH3 563(B1)CH[N(CH3)[(CH2)2N(CH3)2]]CH336(B1)CH(CH3)(n-C3H7) 37 (B1) 1-(1-piperidinyl) ethyl 564 (B17) 1- (4-morpholinyl) ethyl 538 (B1) CH (S-C6H5) CH3; (A+B) 565 (B1) CH [N (CH3) 2]C2H5 539 (B1) CH (O-C6H5) CH3 566 (B1) CH [N (CH3) C2H5)] CH3 540 (B 1) CH (CH3) CH2CN 567 (B1) 1-methyl-3-piperidinyl 541 (B1) CH (C6H5) 2 578 (B1) 1-methyl-2-piperidinyl; (A) 542 (B 1) CH (CZHS) (n-C3H) 569 (B1) 1- (4-methyl-1-piperazinyl) ethyl 543 (B1) CH (n-C3H7) 2 570 (B 1) CH [N (CH3) (n-C3H7)] CH3 544 (B 17 CH (C6H5) CH3 571 (B1) CH [N (CH3) (C2H5-C6H5)] CH3 545 (B 17 5,5,8,8-tetramethyl-5,6,7,8- 572 (B 1) CH [N (CH2-C6H5) 2] CH3 tetrahydro-2-naphtalenyl 546 (B 17 CH (CH3) (n-C5Hl l) 573 (B 1) CH [OC (=O) N (CHZ-C6H5) 2) CH3 787(B17)2,5-diCl-C6H347(B17)CH(C2H5)(n-C5H11) Table 13 R7;sterochemicaldescriptorifCoNoR7;seterochemicaldescriptori fnotoNo Ex No) not racemic and/or addition salut eux No) racemic and/or addition salt 574 (B2) CH3; (E) 94 (B2) 2-furanyl; (E) 575 (B3) 3-pyridinyl; (E) 95 (B2) 2-thienyl; (E) 576 (B3) 4-pyridinyl; (E) 96 (B2) 3-thienyl; (E) 577 (B2) 3-Cl-C6H4 ; (E) 97 (B3) H 578 (B2) 3-CF3-C6H4 98 (B2) 2 (1H)-quinolinone-6-yl ; (E); hydrate (2: 1) 579 (B2) 4-CI-C6H4; (E) 99 (B2) 2-methyl-2H-benzotriazole-5-yl; (E) 580 (B2) 4-CF3-C6H4 ; (E) 00 (B2) 2-benzofuranyl; (E) 581 (B2) cyclohexyl; (E) 01 (B2) 5-methyl-2-furanyl; (E) 582 (B2) 4-OCH3-C6Ii4; (E) 02 (B2) 1-methyl-lH-benzotriazole-6-yl; (E) o No R7 ; stereochemical descriptor if o No R'; stereochemical descriptor if not Ex No) not racemic and/or addition salt (Ex No) racemic and/or addition salt 83 (B2) 4-F-C6H4; (E) 603 (B2) 2 (1H)-quinolinone-4-yl ; (E) 84 (B2) 3-OCH3-C6H4; (E) 604 (B3) 2-pyridinyl; (E) 85 (B2) 2-F-C6H4; (E) OS (B3) 1-methyl-2-pyrrolyl 586 (B2) 3-F-C6H4; (E) 06 (B2), 3,5,6-tetra (F)-4-(OC2H5) phenyl; (E) 587 (B2) (CH2)2C6H5 ; (E) 07 (B2) 2,4-di (F)-C6H3; (E) 588 (B2) CH (CH3) 2; (E) 608 (B2) 3-Br-4-F-C6H3; (E) 89 (B2) CH2C6H5; (E) 609 (B2) 2-F-4-CF3-C6H3; (E) 590 (B2) 6-quinolinyl; (E) 10 (B3) 4-NO2-C6H4; (E) 91 (B2) 2-naphtalenyl; (E) 11(B16) 4-NY2-C6H4 ; (E) 592 (B2) 4-quinolinyl; (E); hydrate (2: 1) 612 (B3) 4-(NHC (=O) CH3)-C6H4; (E) 93 (B2) 1-naphtalenyl ; (E) Table 14 Co No R1,R4 ; stereochemical descriptor if Co No R', R4 ; stereochemical descriptor if Ex No) not racemic and/or addition salt Ex No) not racemic and/or addition salt 13 (B1) 3-CF3-C6H4 ; CH3 632 (B2) CH [N (CH3) 2] CH3; (CH3)=CHC6H5;[A-(E)] 14 (B2) 3-CF3-C6H4; CH2C6H5 633 (B1) CH (CH3) CH2C6H5; CH3 15 (B 1) 3-F-CHd; CH3 634 (B2) H (CH3) CH2C6H5; CH2 (4-CI-C6H4) 16 (B1) 3-F-C6H4; CH3 635 (B15) 1-(methyl-1-piperidinyl) ethyl; CH3 17 (B2) 3-CF3-C6H4; CH=CHC6H5 ; (E) 636 (B2) 1-(methyl-1-piperidinyl) ethyl; H2(4-Cl-C6H4) 618 (B2) 3-F-C6H4; CH=CHC6H5 ; (E) 637 (B1) CH (CH3) (n-C3H7); CH3 19 (B2) 3-F-C6H4; CH2C6H5 638 (B2) H (CH3) (n-C3H7); CH2(4-Cl-C6H4) 620 (B2) 3-F-C6H4; C (CH3) =CHC6H5; (E) ; 639 (B3) H (CH3) (n-C3H7); nitrate (1: 1) CH2 (3,4-diOCH3-C6H3) 21 (B2) CH (C2H5) 2; 1,3-benzodioxolan-2-yl 640 (B3) H (CH3) C2H5; CH2(3,4-diOCH3-C6H3) CH3641(B1)C(CH3)3;CH322(B1)CH2C(CH3)3; 23 (B2) CH2C (CH3) 3; CH2(4-Cl-C6H4) 642 (B3) C (CH3) 3; CH2 (3,4-diOCH3-C6H3); hydrate (1; 1) 24 (B2) CH [C (=O) OC2H5] CH3; 643 (B1) H (n-C3H) Z; CH3 CH2 (4-CI-C6H4) o No R', R4; stereochemical descriptor if o No R', R4; stereochemical descriptor if Ex No) not racemic and/or addition salt Ex No) not racemic and/or addition salt 25 (B1) CH (CH3) C2H5; CH3 644 (B2) H(n-C3H7)2 ; CH2 (3.4-diOCH3- C6H3) 626 (B2) CH (CH3) C2H5; CH2(4-Cl-C6H4) 645 (B 1) CH [N (CH3) 2] C2Hs; CH3; (A) 27 (B1) CH [N (CH3) 2] CH3; CH3; (A) 646 (B3) CH [N (CH3) z) CzHs; CH2 (3,4-diOCH3-C6H3); (A) 628 (B2) CH [N (CH3) 2] CH3; CH2(4-Cl-C6H4) ; 647 (B1) CH [N (C2HS) 2] CH3; CH3; (A) (A) 29 (B3) CH [N (CH3) 2] CH3; 648 (B 1) CH [N (C2HS) 2] CH3; CH3; (A+B) (CH2) 2 (3,4-diOCH3-C6H3); (A) 30 (B3) CH [N (CH3) 2] CH3; 649 (B 3) CH [N (C2H5)2] CH3; CH2 (3, 4,5-triOCH3-C6H2); (A) CH2 (3,4-diOCH3-C6H3); (A) 31(B15)CH[N(CH3)2]CH3;CH3;(B) Table 15 Co No R4, Rb; stereochemical descriptor if o No R4,Rb ; stereochemical descriptor if (Ex No) not racemic and/or addition salt Ex No) not racemic and/or addition salt 650 (B2) H; H 61 (B2) cyclohexyl; H 51 (B2) H; 4-Cl 662 (B2) H; 4-OCH3 652 (B2) H; 3-Cl 663 (B2) H; 4-OC2H5 653 (B2) H; 4-F 64 (B2) H; 2-Cl 54 (B2) H; 3-CF3 65 (B2) H; 3-OCH3 655 (B2) C6H5; H 66 (B3) H; 4-CH3 656 (B2) H; 3-F 67 (B3) H; 3-OH 57 (B2) CH3; H 68 (B3) H; 4-OH 658 (B2) CH (CH3) 2; H 69 (B3) OH; 4-Cl 59 (B2) cyclopentyl; H 70 (B3) OCH3; H; [R- (R*, R*)] + [R- (R*, S*)] 60 (B2) C2H5; H

Table 16 o No yridinyl R', R4; stereochemical o No pyridinyl R, R4; stereochemical (Ex No) position descriptor if not racemic Ex No) osition descriptor if not racemic and/or addition salt and/or addition salt 71(B14 3 CH (CH3) 2; CH3 84 (B3) 3 4-Cl-C6H4 ; CH=C (C6H5) (3-Cl-C6H4) 672 (B2) 3 C6H5; CH=CH-C6H5 85 (B2) 4 CH (CH3) 2; CH2(4-Cl-C6H4) 73 (B 12 3 4-Cl-C6H4 ; CH3 86 (B3) 3 CH (CH3) 2; CH2(4-Cl-C6H4 34-Cl-C6H4;CH=CH=C6H5687(B2)3CH(CH3)2;CH2(4-Cl-C6H4)74(B2) 75 (B2) 3 C6H5; 2OH;CH3688(B13) 76 (B2) 3 4-Cl-C6H4 ; CH=C (C6H5) 2 89 (B 13 3 OH; CH3 44-Cl-C6H4;CH=CC6H5)2690(B31)3CH(CH3)2;NH(3-F-C6H4)77(B3) 78 (B2) 3 3-F-C6H4; CH=CH-C6H5 91 (B31 2 CH (CH3) 2; NH (3-F-C6H4) 79 (B2) 3 CH (CH3) 2; 92(B21 4 CH (CH3) 2; NH (3-F-C6H4) C (CH3) =CH-C6H5; (E) 680 (B3) 2 4-Cl-C6H4 ; CH=C (C6H5) 2 788 (B3) 4 H; CH=C (C6H5) (3-Cl-C6H4) 81 (B2) 4 CH (CH3) 2; 89 (B3) 4 CH (CH3) 2; C (CH3) =CH-C6H5; (E) CH=C (C6H5)(3-Cl-C6H4) 682 (B2) 2 CH (CH3) 2; 90 (B3) 4 cyclohexyl; C (CH3) =CH-C6H5; (E) CH=C (C6H5)(3-Cl-C6H4) 83 (B3) 3 4-CI-C6H4; CH=CH (3-Cl-C6H4) 2

Table 17 methylR1,R4;stereochemicalCoNomethylR1,R4;stereochemicaloNo Ex No) position descriptor if not racemic ; Ex No) position descriptor if not racemic and/or addition salt and/or addition salt 93 (B2) 5 4-Cl-C6H4; 95 (B2) 2 CH (CH3) 2; CH=C(C6H5)(3-Cl-C6H4);CH2(4-Cl-C6H4) (E+Z) 94 (Bl) 2 CH (CH3) 2; CH3 Table 18 Co. Ex. No. R'R4 X Stereochemical No. escriptor if not racemic and/or addition salt 696 B31 CH(CH3)2 CH3 CH 697 B31 CH (CH3) 2 C6H5 CH 698 B25 CH (CH3) 2 C6H5C(=O)- CH 699 B22a CH (CH3) 2 H CH B22b 700 B31 CH (CH3) 2 2F-C6H4 CH 701 B31 CH (CH3) 2 3F-C6H4 CH 702 B25 CH (C2H5) 2 C6H5-C (=O)- CH 703 B22a CH (CI) H5) 2 H CH 704 B27 CH (CH3) [N (CH3) 2] 2-benzothiazolyl CH (A) 705 B27 CH (C2H5) 2 2-benzothiazolyl CH 706 B27 CH (C2H5) 2 2-benzothiazolyl N 791 B25 2, 5-diCl-C6H3 C6H5-C(=O)- CH 792 B22a 2, 5-diCl-C6H3 H H Table 19 No.(Ra)nR1XStereochemicalCo.No.Ex. descriptor if not racemic 707 B31 4-(O-C2H5) CH (CH3) 2 CH 708 B23 3,4-di (OCH3) CH (CH3) 2 CH 709 B31 2,5-di (F) 3- (CF3)-C6H4 CH 710 B31 2,5-di (F) CH (C2H5) 2 CH 711 B31 3-F 3-(CF3)-C6H4 N 712 B31 2,5-di (F) CH (C2HS) 2 N 713 B31 2-F CH (C2H5)2 CH 714 B31 2-F 3- (CF3)-C6H4 CH 715 B31 2-F CH (C2H5) 2 N 716 B31 4-OCH3 3-(CF3)-C6H4 CH Co. No. Ex. No. (Ra)n R1 X Stereochemical descriptor if not racemic 717 B23 3, 4-di (OCH3) CH (CH3) [N (CH3) 2] N (A) 718 B23 3,4-di(OCH3) CH (C2H5) 2 N 719 B23 3,4-dI (OCH3) CH (CH3) [N (CH3)2] CH (A) 720 B23 3,4-di (OCH3) CH (CH3) [N (CH3)2] N (B) 721 B23 3, 4-di (OCH3) CH2-N (CH3) 2 CH 722 B31 4-OCH3 CH (CH3) 2 CH 723 B31 3-F CH (C2H5) 2 N 724 B31 3-F CH (C2H5) 2 CH 725 B31 3-F CH (CH3) 2 N 726 B31 2-F CH (CH3) 2 CH 727 B7 3-NH2 CH (CH3) 2 CH 728 B31 2,5-di (F) CH (CH3) 2 CH 729 B31 3-F 3-(CF3)-C6H4 CH 730 B31 3-CF3 CH (CH3) 2 CH 731 B31 3-F 4-Cl-C6Ha CH 732 B31 3,4-di (CI) CH (CH3) 2 CH 733 B31 3-OCH3 CH (CH3) 2 CH 734 B31 2,4-di (F) CH (CH3) 2 CH 735 B31 3-F C6H5 CH 736 B31 3-CH3 CH (CH3) 2 CH 737 B31 3-NO2 CH (CH3) 2 CH 738 B31 3-Cl CH (CH3) 2 CH 739 B31 4-Cl CH (CH3) 2 CH 740 B31 4-F CH (CH3) 2 CH 741 B31 3-F CH (CH3) 2 CH 742 B31 H CH Table 20 R2R4XHetStereochemicalo.No.R1 (Ex. No.) escriptor if not acemic 43(B29) CH(CH3)2 H 1H-1-imidazolylN-C6H5 44(B29) CH(CH3)2 H N-(3F-1H-1imidazolyl Co. No. Rl RZ R4 X Het tereochemical (Ex. No.) lescriptor if not acemic C6H4) 745 (B2) CH (CH3) 2 CH (CH3) 2-CH2- (4-CI-C6H4) O 1,2,4-triazol-1-yl 46 (B31) CH (CH3) 2 CH (CH3) 2-NH- (3-F-C6H4) 0 IH-1-imidazolyl 47 (B1) CH (CH3) 2 CH (CH3) 2 CH3 O 1,2,4-triazol-1-yl 748 (B1) CH (CH3) 2 H CH3 O 1,2,4-triazol-4-yl 749 (B2) CH (CH3) 2 H-C (CH3) =CH-C6H5 O 1,2,4-triazol-4-yl 50 (B 1) CH (CH3) 2 CH (CH3) 2 CH3 O lH-1-imidazolyl 751 (B2) CH (CH3) 2 CH (CH3) 2-C (CH3) =CH-C6H5 0 IH-1-imidazolyl (E) 752 (B 17) CH3 CH3 CH3 0 IH-1-imidazolyl 753 (B2) CH3 CH3-C (CH3) =CH-C6H5 O 1H-1-imidazolyl 54 (B1) CH (CH3) 2 C2Hs CH3 O 1H-1-imidazolyl 755 (B2) CH (CH3) 2 C2H5 (4-Cl-C6H4)-CH2-0 IH-1-imidazolyl 56 (B1) CZHS CZHS CH O 1H-1-imidazolyl 757 (B 1) CH (C2HS) 2 CH (CH3) 2 CH3 O 1H-1-imidazolyl 758 (B2) CH (CH3) 2 C2Hs-C (CH3) =CH-C6Hs O lH-l-imidazolyl (E) 59 (Bl) CH (CH3) 2 CH3 CH3 O lH-1-imidazolyl 60 (Bl) CH (CH3) 2 n-C4H9 CH3 O 1H-1-imidazolyl 761 (B2) CH (CH3) 2 n-C4Hg-C (CH3) =CH-C6Hs O 1H-1-imidazolyl (E) 762 (B2) CH (CH3) 2 CH (CH3) 2 CHZ- [3, 4-di- O 1H-1-imidazolyl (OCH3)-C6H3] 763 (B2) CH (CH3) 2 CH (CH3) 2-CH2- (4-Cl-c6H4) 0 IH-1-imidazolyl 64 (B28) CH (CH3) 2 H-CHZ- (4-Cl-C6H4) S 1H-1-imidazolyl 765 (B9) CH (C2HS) 2 n-C3H7 CH3 O lH-l-imidazolyl 766 (B2) CH (C2HS) 2 n-C3H7-CH2- (4-Cl-C6H4) 0 IH-1-imidazolyl 767 (B 1) CH (C2HS) 2 C2HS CH3 O 1H-1-imidazolyl 768 (B2) CH (C2HS) 2 C2H5-CH2- (4-Cl-C6H4) 0 1H-1-imidazolyl N 769 (B25) OH H CH3 O C + N 770 (B25) OH H CH3 O C 71 (B24) OH CH (CH3)-CH3 O 1-methyl-5- N (CH3) 2 midazolyl 772 (B24) OH CH (C2HS) 2 CH3 O l-methyl-5- imidazolyl R2R4XHetStereochemicalCo.No.R1 ifnotEx.No.descriptor acemic 773 (B31) CH (CH3) 2 H -NH-(3-F-C6H4) O 2-methyl-1- imidazolyl 93 (B33) 4-Cl-C6H4 H H O 1-methyl-5- imidazolyl 94 (B3) 4-CI-C6Hq OH CH (OH) (3-Cl-C6H4) O 1-methyl-5- imidazolyl 795 (B3) 4-Cl-C6H4 H CH (OH) (3-Cl-C6H4) O 1-methyl-5- imidazolyl 96(32) -S-CH3NH1H-1-imidazolylH C6H3 97 (B29) 2, 5-diCl- H -NH-CH3 NH IH-1-imidazolyl HCI (1: 2) C6H,- ; Table 20 Co. No. R4 n (Ex.No.) 774 (B 17)-CHZ- (4-Cl-C6H4) 3 775 (B17) CH3 3 776 (B 17) 1 CH3 14 Table 21 lists the experimental elemental analysis values for carbon, hydrogen and nitrogen of some of the compound as prepared in the experimental part hereinabove.

Table 21 Comp C H N Comp C H N Comp C H N No. No. No. 17 64.0 6.2 12.7 64 65.9 5.8 16.3 123 74.0 7.9 10.3 18 63.8 6.3 13.0 85 70.8 7.7 13.8 125 74.3 8.1 10.0 20 63.5 6.7 12.8 86 70.7 7.8 13.9 131 64.7 5.7 15.2 21 64.2 6.6 12.8 87 69.6 6.7 10.6 142 69.6 6.8 11.0 30 72.3 8.3 8.4 119 71.3 7.5 10.0 143 62.7 5.2 10. 3 52 72.0 8.1 9.3 120 75.1 7.0 8.4 145 71.4 7.0 15.2 53 68.7 8.6 12.2 121 74.4 6.9 11.9 147 72.1 7.0 15.4 61 74.2 8.2 10.0 122 73.9 7.9 10.2 148 52.6 5.0 11.5 Comp C H N Comp C H N Comp C H N No. No. No. 152 72.3 7.2 16.0 417 71.2 6.0 9.0 514 75.2 6.2 8.4 154 73.5 6.8 15.7 419 75.1 6.4 9.5 515 73.7 5.8 9.1 162 66.9 5.9 14.0 420 75.2 5.5 11.0 521 69.9 7.4 16.3 163 70.2 7.8 15.3 425 72.9 5.1 10.2 523 70.0 5.2 13.6 164 76.9 7.6 11.6 426 72.9 5.5 9.6 524 63.4 4.5 11.7 194 71.0 6.4 17.5 438 65.5 7.2 16.1 566 67.6 8.1 18.6 237 70.6 6.5 10.7 445 79.6 5.9 10.7 572 76.2 7.1 12.7 247 71.7 6.6 16.6 454 79.9 6.3 10.0 574 71.4 7.7 14.0 248 69.4 5.6 11.5 455 77.0 7.0 11.7 575 73.3 6.8 15.6 259 50.5 4.3 16.5 456 79.5 6.7 9.5 576 73.2 6.7 15.6 260 50.6 4.4 16.6 457 77.3 7.4 11.2 577 69.5 6.0 10.6 298 60.1 6.0 16.5 458 76.5 7.1 11.5 578 67.3 5.6 9.8 299 60.7 6.0 16.5 459 76.3 7.1 11.5 579 69.7 6.1 10.5 318 68.2 7.3 13.5 460 75.4 6.6 12.0 580 67.4 5.6 9.8 343 68.9 6.5 14.8 461 72.0 6.0 11.3 581 75.6 8.6 11.4 348 69.6 7.5 12.7 462 77.0 7.3 11.2 582 73.7 7.0 10.7 349 65.1 8.2 22.5 463 78.1 7.4 10.4 583 73.3 6.4 11.1 360 69.3 6.6 10.5 464 77.1 7.6 10.7 584 73.4 7.0 10.5 367 67.0 6.2 14.3 465 77.5 7.8 10.4 585 72.9 6.4 11.1 368 65.1 6.2 13.8 466 75.6 6.3 12.6 586 72.9 6.4 11.1 369 67.5 5.1 8.9 467 76.9 7.0 11.7 587 76.4 7.5 10.6 376 62.7 4.5 8.3 468 80.8 6.8 9.0 588 74.1 8.6 13.2 383 69.4 7.6 12.1 469 77.4 6.5 11.7 589 77.2 7.4 11.2 389 69.5 7.5 11.0 470 77.8 7.1 10.8 602 68.6 6.2 19.8 391 67.2 7.1 11.7 471 77.6 7.7 10.9 612 71.9 6.8 13.5 392 68.3 7.4 12.7 472 78.2 7.5 10.1 613 59.8 4.2 15.3 394 64.8 6.2 9.0 482 77.2 7.6 10.8 614 65.9 4.4 12.7 397 66.2 6.3 10.3 483 73.5 6.0 9.1 615 65.8 4.9 18.2 402 64.6 6.5 9.6 484 73.7 6.2 9.1 616 65.7 4.7 18.2 404 67.9 6.9 9.8 485 81.8 5.9 8.6 617 66.9 4.1 12.4 405 67.9 7.0 9.7 497 78.7 5.6 10.8 618 72.1 4.7 14.0 410 66.9 7.2 11.8 502 75.9 6.6 12.0 619 71.3 4.9 14.6 411 69.8 7.1 12.1 511 79.7 6.4 9.9 620 64.5 4.7 14.2 414 68.9 7.6 12.1 512 72.8 5.2 9.6 636 66.0 6.6 14.9 415 71.6 7.2 10.8 513 74.8 6.2 8.9 644 67.4 7.3 11.5 Comp C H N Comp C H N Comp C H N No. No. 650 75.1 6.8 12.5 704 60.3 5.7 18.7 786 67.0 4.5 8.9 666 76.1 7.4 11.9 705 63.3 6.2 15.7 788 76.0 4.9 6.5 667 71.9 6.5 11.9 706 60.5 5.4 19.2 789 76.9 5.8 5.9 676 79.3 5.1 5.5 720 61.5 6.6 19.3 793 66.1 4.9 12.7 677 79.8 5.1 5.5 734 64.8 5.4 15.2 794 61.8 4.4 8.4 679 80.8 7.0 7.4 749 73.4 6.7 15.6 795 63.5 4.6 8.6 680 78.9 5.0 5.6 771 63.9 7.7 17.2 797 46. 9 4.6 14. 5 681 81.4 7.2 7.5 777 65.1 5.6 17.2 682 80.8 7.1 7.5 782 70.6 7.7 13.9 695 68.0 6.2 10.7 783 70. 5 7.7 113.8

C. examples Example C. 1: Inhibition of retinoic acid (RA) metabolism MCF-7 human breast cancer cells were grown as stock cultures according to art-known protocols. One day before the experiment, RA is added to the stock cultures to stimulate RA-metabolism. At the start of the experiment, cell suspensions were incubated in a tissue culture medium containing 3H-RA as the substrat. Different concentrations of the test compound (dissolve in 1 % DMSO) were added to the incubation mixtures, and at the end of the incubation, the unmetabolized RA is separated from its polar metabolites.

The fraction containing the polar 3H-labelled metabolites was collecte and counted in a scintillation conter. For each experiment, a control and a blank incubation were run in parallel. Table 22 list the IC50 value (defined as the concentration in M needed to reduce the amount of metabolites to 50 % of the control). Table 22 Co. IC50 Co. IC50 Co. IC50 Co. IC50 Co. IC50 Co. IC50 No. (in M) No. (in (inM)No.(inM)No.(inM)No.No. 1 138E-10 13 3.57E-11 28 2.76E-09 38 1.04E-09 52 9.07E-10 67 3.34E-10 2 3. 00E-11 17 9.99E-10 29 8.12E-09 39 1.04E-10 53 2.12E-09 68 1.72E-09 4 2. 11D-09 18 8.72E-10 30 2.58E-08 41 1.98E-09 54 4.86E-09 69 2.50E-10 5 2.70E-10 21 2.89E-09 31 2.63E-09 45 1.72E-10 56 2. 51E-11 70 2.95E-10 6 1.65E-09 22 1.04E-09 32 6.97E-10 46 1.95E-09 58 <.00E-11 71 2.62E-10 7 7.90E-10 23 5.03E-10 33 1. OlE-09 47 1.33E-09 61 7.34E-10 72 1.66E-09 8 937E-11 24 1.37E-09 34 1.03E-09 48 5.69E-10 63 6.70E-09 73 4.63E-10 10 6.10E-08352.24E-9494.33E-10646.60E-09754.17E-10$25 11 2.63E-09 26 2.01E-10 36 1.43E-09 50 7.44E-09 65 3.79E-10 76 5.88E-10 12 3.65E-11 27 2.32E-10 37 1. OOE-09 51 8.95E-10 66 3.56E-10 77 332E-10 Co. IC50 Co. IC50 Co. IC50 Co. IC50 Co. IC50 Co. IC50 No. (in M) No. (in M) No. (in M) No. (in M) No. (in M) No. (in M) 78 2.27E-10 116 6.78E-10 156 3.10E-08 194 7.07E-09 23 | 1. 51E-09 27 | 5. 61E-09 79 3. 42E-11 117 2.55E-10 157 8.48E-08 195 3.51E-08 233 2.43E-09 271 2.45E-09 80 4.83E-11 118 2.24E-09 158 >1. 00E-07 196 2.23E-08 234 3. 01E-09 272 4.81E-09 81 2.31E-10 119 9.40E-10 159 >1. 00E-07 197 5. 61E-09 235 6. 94E-09 273 5.27E-08 82 1.16E-09 120 3.88E-09 160 8.65E-08 198 1.07E-08 236 9.84E-08 274 6.64E-09 83 1.62E-10 121 9.14E-10 161 1. 87E-09 199 7.82E-09 237 1.82E-08 275 4.28E-09 84 1.74E-09 122 2.40E-09 162 2.88E-09 200 4.43E-08 238 >1. OOE-07 276 1.60E-08 85 3.92E-09 123 2. 47E-11 163 2.36E-09 201 3.58E-09 239 728E-10 277 1.17E-09 86 4.97E-10 124 3.97E-11 164 8.15E-09 202 1.84E-09 240 134E-09 288 1.28E-09 87 2. 80E-10 125 1.94E-10 165 1.08E-08 203 228E-08 241 2.59E-09 289 5. 07E-10 88 1. 48E-10 126 <1.00E-11 166 1.75E-09 204 4.58E-09 242 2.82E-09 290 1.14E-09 89 1.31E-10 127 2.85E-11 167 4.16E-09 205 1.17E-08 243 3.59E-08 291 4.23E-09 90 2.36E-09 128 1.81E-11 168 2.36E-09 207 2.54E-08 244 2.30E-09 292 1. 37E-10 91 9.35E-10 129 2. 36E-11 169 5.31E-10 208 6.43E-09 245 2.79E-09 293 6.53E-09 92 2.21E-09 130 1.09E-11 170 1.22E-08 209 8.27E-09 246 2.10E-09 297 7.86E-10 93 1.59E-09 131 4. 10E-09 171 8.58E-08 210 2.90E-08 247 3.55E-08 299 7.72E-10 94 1.06E-09 132 4.49E-09 172 3. 41E-09 212 4.07E-09 248 1.79E-09 301 6. 05E-09 95 1.48E-09 133 4.56E-09 173 5.17E-09 213 2.07E-09 249 7.58E-08 303 3.26E-09 96 1.09E-09 134 2.98E-09 174 1.60E-09 214 3. 37E-09 250 1.49E-08 305 8. 29E-11 97 1.32E-09 135 1.43E-09 175 4.83E-09 215 3.60E-08 251 3.93E-09 306 1.26E-09 98 1.64E-09 136 4.83E-09 176 1.87E-08 216 1.17E-08 252 2.59E-09 307 7. OIE-10 99 5.77E-09 137 1.85E-09 179 3.69E-08 217 5.14E-09 253 5. 55E-09 309 3.65E-09 102 6. 78E-11 138 6.38E-09 190 5.69E-08 219 3.20E-09 254 6.47E-09 311 6.64E-10 103 7. 11E-09 139 1.75E-09 181 1.41E-08 220 1.48E-09 255 6.24E-09 313 2.00E-11 104 4. 07E-1 140 2.15E-08 182 1.31E-08 221 1.08E-09 256 3.20E-09 316 4.06E-09 105 5.16E-11 141 1.31E-09 183 7.40E-09 222 3.32E-09 259 9.29E-09 330 1.82E-09 106 1.69E-09 142 3. 11E-08 184 5.15E-09 223 1. 20E-09 260 2.43E-09 332 1.50E-09 107 1.44E-09 143 4.08E-09 185 3.97E-08 224 4.73E-09 261 2.22E-09 336 1.91E-09 108 2.34E-11 145 3.03E-09 186 >1.00E-07 225 8.28E-08 262 7.48E-09 339 1.23E-09 109 3.21E-10 147 3.30E-08 187 1.88E-08 226 1.69E-08 263 4.66E-09 346 2.04E-09 110 9.53E-10 148 1.86E-09 189 >1. 00E-07 227 7.80E-09 264 2.71E-09 351 5.69E-09 111 1.03E-09 151 2. 11E-09 190 >1.00E-07 228 7. 30E-08 266 3. 11E-08 352 2. 57E-10 112 9.89E-10 152 5. 18E-09 191 >1.00E-07 229 1. 64E-09 267 7.75E-09 353 1,97E-09 113 8.52E-10 154 4.14E-09 192 3.34E-09 230 3.89E-09 268 7.79E-09 355 >1.00E-07 115 8.17E-09 155 5.01E-08 193 1. 21E-08 231 1.86E-09 269 2.66E-09 336>1.00E-07 Co. IC50 Co. IC50 Co. IC50 Co. IC50 Co. IC50 Co. IC50 No. (in M) Nu (in M) No. (in M) No. (in M) No. (in M) No. (in M) 357 >1. OOE-07 426 >1. OOE-07 484 3.43E-09 587 3.16E-08 639 1.68E-09 690 >1. OOE-07 358 >1. OOE-07 427 8.34E-09 485 >1.00E-07 588 4.88E-08 640 2.17E-09 691 >1.00E-07 359 6.25E-09 432 8. 10E-10 486 2.77E-08 589 2.75E-09 642 1.16E-09 692 3.80E-08 360 1.08E-09 435 2.80E-09 488 >1.00E-07 590 2.78E-09 644 2.96E-10 693 >1. OOE-07 361 >1.00E-07 445 1.92E-07 489 >1.00E-07 591 4. OIE-09 645 8.02E-09 695 >I. OOE-07 362 1.43E-08 454 5.25E-08 490 >1. OOE-07 592 4.15E-09 646 07E-096968.07E-093. 363 1.42E-09 455 2.87E-09 491 1.84E-09 593 2.70E-09 649 7. 32E-09 697 1. 71E-08 364 1. 41E-09 456 1.40E-07 492 4.07E-09 594 4. 81E-09 650 4.86E-09 698 3.96E-08 365 1.08E-09 457 2.50E-08 493 8.77E-09 595 3.83E-09 651 l. OSE-08 699 9.69E-09 366 3. OSE-09 458 3.22E-09 497 3.76E-08 596 7.92E-09 652 >1.00E-07 700 1.20E-08 367 1.25E-09 459 1.77E-08 502 3.29E-08 597 5. OOE-09 653 1.34E-09 707 1.30E-08 368 5.83E-10 460 3.63E-08 511 1. 05E-08 598 2.39E-08 654 2.34E-09 708 1. 61E-09 369 8.22E-08 461 1.69E-08 512 6.16E-07 599 6.36E-09 655 1. 61E-08 709 2.40E-09 370 8.34E-08 462 >1. OOE-06 513 8.60E-07 600 3.67E-08 656 1.47E-09 710 1.88E-10 371 3.59E-09 463 2.45E-08 514 >1. OOE-06 601 2. 00E-08 657 5.36E-09 711 >1. OOE-07 372 1.97E-09 464 1.49E-07 515 >1.00E-06 602 2.57E-08 658 5.48E-09 712 4.30E-12 376 <1. OOE-10 465 5.04E-08 516 >1.00E-06 603 >1. OOE-07 659 >1. OOE-07 713 1.38E-09 378 1.74E-09 466 >I. OOE-06 517 3.69E-08 604 2.89E-09 660 6. 37E-09 715 1.54E-10 383 7.29E-10 467 2.58E-09 518 >1. OOE-07 605 1.40E-08 661 3.40E-08 718 1.33E-10 385 6.75E-09 468 >1.00E-07 519 3.80E-09 606 1.36E-08 662 3.58E-10 722 4.14E-09 388 8.29E-10 469 >1.00E-07 524 >1. OOE-06 608 6. 61E-09 663 1.95E-09 723 1.13E-09 389 5. 67E-11 470 1.87E-08 558 1.32E-09 609 1.09E-08 664 1.56E-09 724 1.18E-09 393 9.55E-10 471 >1. OOE-07 574 1.78E-09 610 6.53E-09 665 5. 91E-09 725 3.29E-09 404 1.35E-09 472 9.51E-08 575 2.57E-08 611 3.42E-09 666 1.45E-08 726 3.7lE-09 405 3.68E-09 473 >1. OOE-07 576 2. OIE-08 612 1.68E-08 667 1.57E-09 727 1.64E-09 412 3.99E-09 474 1.59E-08 577 4.23E-08 613 1.80E-06 668 3.16E-09 728 1. 41E-09 413 5.27E-09 475 >1.00E-07 578 7.67E-09 614 2.78E-07 669 8.66E-09 729 >1.00E-07 415 2.64E-09 476 3.55E-08 579 1.24E-08 615 >1. OOE-06 670 5.72E-09 730 1.59E-08 416 3.67E-10 477 >1. OOE-06 580 3.13E-08 616 >1. OOE-06 67 |>1. OOE-06 731 >1. OOE-07 420 8.38E-08 478 1.63E-09 581 >1. OOE-07 617 l. 5lE-07 680 1.21E-08 732 1.93E-08 421 >1. 00E-07 479 >1. OOE-07 582 1.58E-09 618 1.57E-08 681 >I. OOE-06 733 2.41E-09 422 >I. OOE-08 480 4. 25E-09 583 2.78E-09 619 3.57E-08 682 >1. OOE-07 734 2.25E-09 423 4.08E-08 481 2.83E-09 584 6. 51E-09 620 >1.00E-06 685 9. 08E-08 735 >1.00E-07 424>1. OOE-07 482 1. 95E-09 585 7.21E-09 621 1.25E-09 686 4.31E-08 736 7.45E-09 425 1.98E-085863.74E-096231.38E-09687>1.00E-077372.36E-09483 Co. IC50 Co. IC50 Co. IC50 Co. IC50 Co. IC50 Co. IC50 No. (in M) No. (in M) No. (in M) No. (in M) No. (in M) No. (in M) 738 2.03E-09 743 1. 10E-08 751 6.70E-08 762 4.08E-08 774 5.27E-09 782 1.26E-09 739 4. 21E-08 744 >1. OOE-07 753 >I. OOE-07 763 5.62E-09 776 4.39E-09 783 3.98E-08 740 1.29E-09 745 3.87E-09 755 4.35E-09 764 2.33E-08 778 7.59E-08 741 1.44E-09 746 >I. OOE-07 758 1.88E-09 772 1.46E-10 780 4.57E-09 742 2. 61E-10- 749 1.26E-07 761 >1. OOE-07 773 >I. OOE-07 781 3. 24E-09

Example C. 2:"Vaginal Keratinization Test on Ovariectomized Rats" Ovariectomized rats were injecte subcutaneously with a sesame oil solution containing 100 Rg of estradiol undecylate in a volume of 0.1 ml per 100 g body weight and control animals were injecte with sesame oil. On day one, two and three, test <BR> <BR> animals were treated once daily with a per os dose of the test compound and control animals with the drug vehicle (PEG 200). One day after the last treatment, the animals were sacrifice and their vaginas were processed for histological evaluation according to the method described in J. Pharmacol. Exp. Ther. 261 (2), 773-779 (1992). A dose at which 50 % of the tested rats show complete suppression of the estradiol undecylate induced keratinization effects is defined as an active dose. Table 23 lists the lowest active dose (LAD in mg/kg) of the compound of formula (I) which were tested.

Table 23 Co. AD Co. LAD Co. LAD Co. AD Co. AD Co. AD No. mg/kg) No. (mg/kg) No. (mg/kg) No. (mg/kgA No. m 2 5.00 24 2.50 41 2.50 61 2.50 77 2.50 93 2.50 3 >2.50 25 10.00 43 2.50 62 >5.00 78 1.25 94 5.00 4 0.60 26 5.00 44 2.50 63 >5.00 79 2.50 95 5.00 5 >2.50 27 5.00 45 2.50 64 >5.00 80 >2.50 96 2.50 6 2.50 28 2.50 46 >2.50 65 5.00 81 2.50 97 2.50 7 >2.50 29 5.00 47 2.50 66 2.50 82 2.50 98 5.00 8 >2.50 30 00482.50672.5083>5. >2.50 99 2.50 10 2.50 31 5.00 49 2.50 68 5.00 84 >2.50 102 5.00 11 >2.50 32 5.00 50 2.50 69 2.50 85 2.50 103 >2.50 13 >2.50 33 5.00 52 2.50 70 5.00 86 2.50 104 2.50 15 >2.50 34 2.50 53 >2.50 71 >5.00 87 1.25 105 2.50 18 2.50 35 2.50 55 >2.50 72 2.50 88 2.50 106 2.50 20 2.50 36 5.00 56 >5.00 73 >2.50 89 2.50 107 >2.50 21 5.00 37 5.00 57 >5.00 74 2. 50 90 2. 50 109 2. 50 22 2.50 38 5.00 58 5.00 75 2.50 91 2.50 110 >2-50 390.6059>2.5076>2.50925.00111>2.50232.50 Co. LAD Co. LAD Co. LAD Co. LAD Co. LAD No. (mg/kg)No.(mg/kg)No.(mg/kg)No.(mg/kg)No.(mg/kgNo. 112 2.50 157 >10.00 194 10.00 234 10.00 274 >10.00 315 >2.50 113 >2.50 158 >10.00 195 >10.00 235 5.00 275 >10.00 316 5.00 114 2.50 159 >10.00 196 >10.00 236 5.00 276 >10.00 317 >5.00 115 >2.50 160 10.00 197 >10.00 237 5.00 277 >5.00 318 >2.50 116 2.50 161 >2.50 198 >10.00 238 5.00 278 2.50 319 >5.00 117 >2.50 162 >5.00 199 >10.00 239 10.00 279 2.50 320 5.00 118 2.50 163 20.00 200 >10.00 240 10.00 280 >2.50 322 >2.50 121 >2.50 164 20.00 201 >10.00 241 10.00 281 >2.50 324 >2.50 122 >2.50 165 >20.00 202 >10.00 242 >10.00 283 2.50 325 2.50 123 2.50 166 5.00 203 >10.00 243 10.00 284 2.50 326 >2.50 125 2.50 167 10.00 204 >10.00 244 10.00 285 >2.50 327 >2.50 126 2.50 168 10.00 205 >10.00 245 10.00 286 >2.50 328 >2.50 127 >2.50 169 10.00 207 10.00 246 10.00 287 >2.50 329 >2.50 128 5.00 170 10.00 208 >10.00 247 10.00 288 >2.50 330 2.50 129 2.50 171 >10.00 209 5.00 248 2.50 289 >2.50 332 >2.50 130 5.00 172 10.00 210 20.00 249 5.00 290 2.50 333 >2.50 131 5.00 173 10.00 212 20.00 250 >10.00 291 >2.50 337 2.50 132 5.00 174 10.00 213 20.00 251 10.00 292 >2.50 338 >2.50 133 >5.00 175 10.00 214 20.00 252 >10.00 293 >2.50 339 >2.50 134 5.00 176 >10.00 215 20.00 253 >5.00 294 >2.50 340 2.50 135 2.50 178 >10.00 216 20.00 254 >5.00 295 >2.50 341 >2.50 136 5.00 179 >10.00 217 10.00 255 5.00 297 >2.50 342 >2.50 137 >5.00 180 >10.00 219 20.00 256 >2.50 300 >2.50 343 >2.50 138 >5.00 181 10.00 220 20.00 261 >10.00 301 >2.50 346 >5,00 139 10.00 182 10.00 221 10.00 262 20.00 302 >2.50 347 >5.00 140 5.00 183 >10.00 222 20.00 263 >10.00 304 >2.50 348 >2.50 141 >10.00 184 >10.00 223 5.00 264 >10.00 306 >2.50 349 >2.50 142 5.00 185 10.00 224 >10.00 266 >10.00 307 >2.50 350 >2.50 143 10.00 186 >10.00 227 >10.00 267 >10.00 308 >2.50 351 >5.00 148 >5.00 187 >10.00 228 >10.00 268 >10.00 309 >2.50 352 >5.00 151 5.00 189 >10.00 229 >10.00 269 >10.00 310 2.50 353 >5.00 152 >5.00 190 >10. 00 230 >10. 00 270 >10. 00 311 2.50 354 >5.00 154 5.00 191 >10.00 231 >10. 00 271 10.00 312 >2.50 355 >10. 00 155 >10.00 192 >10.00 232 >10.00 272 >10.00 313 2.50 356 >10. 00 156 >10. 00 193 >10. 00 233 >10.00 273 >10.00 314 >2.50 357 >10.00 Co. LAD Co. LAD Co. LAD Co. LAD Co. LAD Co. LAD No. mg/kg) No. (mg/k No. (mg/kg No. (mg/kg) No. (mg/kg) No. m/k 358 >10.00 397 >2.50 436 >5.00 484 >5.00 576 10.00 612 10.00 359 >10.00 398 >5.00 437 >2.50 485 5.00 577 10.00 613 >20.00 360 2.50 400 >2.50 438 >2.50 486 5.00 578 >10.00 614 >20.00 361 10.00 401 >2.50 439 >2.50 487 >5.00 579 10.00 615 >20.00 362 10.00 402 >5.00 445 >20.00 489 2.50 580 10.00 618 >20.00 363 >10.00 403 >5.00 454 >20.00 490 2.50 581 20.00 619 >20.00 364 2.50 404 5.00 455 2.50 492 >2.50 582 >10.00 621 1.25 365 10.00 405 5.00 456 >20.00 493 >2.50 583 10.00 623 >5.00 366 >10.00 406 >5.00 457 >20.00 494 >2.50 584 10.00 624 >2.50 367 2.50 407 >5.00 458 5.00 495 >2.50 585 10.00 626 2.50 368 2.50 408 >5.00 459 20.00 497 >20.00 586 >10.00 627 >2.50 369 10.00 409 5.00 460 >20.00 502 5.00 587 >10.00 628 >2.50 370 >10.00 410 >5.00 461 10.00 511 >20.00 588 10.00 629 S2.50 371 10.00 411 2.50 462 20.00 512 >20.00 589 10.00 630 >2.50 372 5.00 412 >2.50 463 20.00 513 >20.00 590 >10.00 631 >2.50 374 2.50 413 5.00 464 >20.00 514 >20.00 591 >10.00 632 >2.50 375 >5.00 414 5.00 465 >20.00 515 >20.00 592 >10.00 636 2.50 376 2.50 416 >5.00 466 >20.00 518 >10.00 593 >10.00 638 >2.50 378 2.50 417 >5.00 467 >20.00 519 >10.00 594 >10.00 639 2.50 379 >2.50 419 >5.00 468 10.00 521 10.00 595 10.00 640 >2.50 380 >2.50 420 >20.00 469 >10.00 524 20.00 596 10.00 642 2.50 381 >2.50 421 >10.00 470 >20.00 532 >10.00 597 >10.00 644 2.50 383 >2.50 422 >10.00 471 >10.00 551 >2.50 598 >10.00 645 >5.00 384 >2.50 423 20.00 472 >20.00 552 >2.50 599 >20.00 646 5.00 385 >2.50 424 >10.00 473 >10.00 554 2.50 600 >10.00 647 >5.00 386 >2.50 425 >10.00 474 >10.00 555 >2.50 601 10.00 649 5.00 387 >2.50 426 >10.00 475 >10.00 557 >5.00 602 >10.00 650 10.00 389 >2.50 427 2.50 476 >10.00 558 >5.00 603 >10.00 651 5.00 390 >2.50 428 >2.50 477 >10.00 560 >5.00 604 >10.00 652 10.00 391 >5.00 429 >2.50 478 2.50 562 5.00 605 >10.00 653 5.00 392 >5.00 431 >2.50 479 >10.00 566 5.00 606 >10.00 654 5.00 393 5.00 432 >2.50 480 10.00 570 >5.00 608 >10.00 655 >10.00 394 >2.50 433 >2.50 481 10.00 572 >5.00 609 10.00 656 10.00 395 >5. 00 434 >2.50 482 10.00 574 20.00 610 >10.00 657 >10.00 396 >2.50 435 >2.50 483 >5.00 575 20.00 611 10.00 658 >10.00 Co. LAD Co. LAD Co. LAD Co. AD Co. AD Co. LAD No. (mg/kg, No. (mg/kgl No. (mg/kg No. mg/k No. (mg/kg No. mg/k 659 >10.00 681 >20.00 708 >5.00 723 5.00 738 10.00 762 >5.00 660 >10.00 682 >20.00 709 5.00 724 2.50 739 >10.00 763 >5.00 661 >10.00 686 >10.00 710 2.50 725 5.00 740 20.00 764 >5.00 662 5.00 690 >10.00 711 5.00 726 5.00 741 10.00 766 >2.50 663 2.50 692 >10.00 712 5.00 727 >10.00 742 10.00 768 >2.50 664 5.00 695 >10. 00 713 2.50 728 5.00 743 >10. 00 772 >5.00 665 2.50 696 >10.00 714 2.50 729 2.50 745 >5.00 773 >10.00 666 2.50 697 10. 00 715 >2.50 730 >10.00 746 >5.00 774 10.00 667 5.00 698 20.00 716 >2.50 732 >10.00 749 >20.00 776 >20.00 668 5.00 700 5.00 717 >2.50 733 >10. 00 751 10.00 778 5.00 669 5.00 704 >5.00 718 2.50 734 10.00 753 >10.00 782 2.50 670 >2.50 705 >5.00 720 >2.50 735 10.00 754 10.00 783 5.00 679 >20.00 706 5.00 721 >2.50 736 >10.00 758 >5.00 784 >5.00 680 >20.00 707 5. 00 722 5.00 737 >10.00 761 >5.00 785 5.00

D. Composition examples The following formulations exemplify typical pharmaceutical compositions suitable for systemic or topical administration to animal and human subjects in accordance with the present invention."Active ingredient" (A. I.) as used throughout these examples relates to a compound of formula (I) or a pharmaceutically acceptable acid addition salt thereof.

Example D. 1: oral solution 9 g of methyl 4-hydroxybenzoate and 1 g of propyl 4-hydroxy-benzoate were dissolve in 41 of boiling purifie water. In 3 1 of this solution were dissolve first 10 g of 2,3-dihydroxybutanedioic acid and thereafter 20 g of A. I. The latter solution was combine with the remaining part of the former solution and 121 1,2,3-propane-triol and 3 1 of sorbitol 70% solution were added thereto. 40 g of sodium saccharin were dissolve in 0.5 1 of water and 2 ml of raspberry and 2 ml of gooseberry essence were added. The latter solution was combine with the former, water was added q. s. to a volume of 201 providing an oral solution comprising 5 mg of A. I. per teaspoonful (5 ml). The resulting solution was filled in suitable containers.

Example D. 2: oral drops 500 g of the A. I. was dissolve in 0.5 1 of 2-hydroxypropanoic acid and 1.5 l of the polyethylene glycol at 60~80°C. After cooling to 30-40°C there were added 35 1 of polyethylene glycol and the mixture was stirred well. Then there was added a solution of 1750 g of sodium saccharin in 2.5 1 of purifie water and while stirring there were

added 2.5 1 of cocoa flavor and polyethylene glycol q. s. to a volume of 50 l, providing an oral drop solution comprising 10 mg/ml of A. I. The resulting solution was filled into suitable containers.

Example D. 3: capsules 20-ouf A. I., 6 g sodium lauryl sulfate, 56 g starch, 56 g lactose, 0.8 g colloidal silicon dioxide, and 1.2 g magnesium stearate were vigorously stirred together. The resulting mixture was subsequently filled into 1000 suitable hardened gelatin capsules, each comprising 20 mg of A. I.

Example D. 4: injectable solution 0.5 mg A. I. 1,50 mg glucose anhydrous and 0.332 ml concentrated hydrochloric acid were mixed with 0.8 ml water for injections. Sodium hydroxide was added until pH = 3.2 0.1 alld water was added to 1 ml. The solution was sterilized and filled in sterile containers.

Example D. 5: film-coated tablets tabletcorePreparationof A mixture of 100 g of the A. I., 570 g lactose and 200 g starch was mixed well and thereafter humidifie with a solution of 5 g sodium dodecyl sulfate and 10 g polyvinyl- pyrrolidone (Kollidon-K 90 (D) in about 200 ml of water. The wet powder mixture was sieved, dried and sieved again. Then there was added 100 g microcrystalline cellulose (Avicel (E)) and 15 g hydrogenated vegetable oil (Sterotex 0). The whole was mixed well and compresse into tables, giving 10.000 tables, each comprising 10 mg of the active ingredient.

Coating To a solution of 10 g methyl cellulose (Methocel 60 HG O) in 75 ml of denaturated ethanol there was added a solution of 5 g of ethyl cellulose (Ethocel 22 cps @) in 150 ml of dichloromethane. Then there were added 75 ml of dichloromethane and 2.5 ml 1,2,3-propanetriol. 10 g of polyethylene glycol was molten and dissolve in 75 ml of dichloromethane. The latter solution was added to the former and then there were added 2.5 g of magnesium octadecanoate, 5 g of polyvinylpyrrolidone and 30 ml of concentrated color suspension (Opaspray K-1-2109 #) and the whole was homogenated. The tablet cores were coated with the thus obtained mixture in a coating apparats.

Example D. 6: 2% cream 75 mg stearyl alcool, 2 mg cetyl alcool, 20 mg sorbitan monostearate and 10 mg isopropyl myristate are introduced into a doublewall jacketed vessel and heated until

the mixture has completely molten. This mixture is added to a separately prepared mixture of purifie water, 200 mg propylene glycol and 15 mg polysorbate 60 having a temperature of 70 to 75°C while using a homogenizer for liquids. The resulting mulsion is allowed to cool to below 25°C while continuously mixing. A solution of 20 mg A. I., 1 mg polysorbate 80 and purifie water and a solution of 2 mg sodium sulfite anhydrous in purifie water are next added to the mulsion while continuously mixing.

The cream, 1 g of the A. I. is homogenized and filled into suitable tubes.

Example D. 7: 2% topical gel To a solution of 200 mg hydroxypropyl ß-cyclodextrine in purifie water is added 20 mg of A. I. while stirring. Hydrochloric acid is added until complete dissolution and then sodium hydroxide is added until pH 6.0. This solution is added to a dispersion of 10 mg carrageenan PJ in 50 mg propylene glycol while mixing. While mixing slowly, the mixture is heated to 50°C and allowed to cool to about 35°C whereupon 50 mg ethyl alcohol 95% (v/v) is added. The rest of the purifie water q. s. ad 1 g is added and the mixture is mixed to homogenous.

Example D. 8: 2 % topical cream To a solution of 200 mg hydroxypropyl-cyclodextrine in purifie water is added 20 mg of A. I. while stirring. Hydrochloric acid is added until complete dissolution and next sodium hydroxide is added until pH 6.0. While stirring, 50 mg glycerol and 35 mg polysorbate 60 are added and the mixture is heated to 70°C. The resulting mixture is added to a mixture of 100 mg mineral oil, 20 mg stearyl alcool, 20 mg cetyl alcool, 20 mg glycerol monostearate and 15 mg sorbate 60 having a temperature of 70°C while mixing slowly. After cooling down to below 25°C, the rest of the purifie water q. s. ad 1 g is added and the mixture is mixed to homogenous.

Example D. 9: 2% liposome formulation A mixture of 2 g A. I. microfine, 20 g phosphatidyl choline, 5 g cholesterol and 10 g ethyl alcohol is stirred and heated at 55-60°C until complete dissolution and is added to a solution of 0.2 g methyl paraben, 0.02 g propyl paraben, 0.15 g disodium edetate and 0.3 g sodium chloride in purifie water while homogenizing. 0.15 g Hydroxypropyl- methylcellulose in purifie water ad 100 g is added and the mixing is continued until swelling is complet.