BACKGROUND OF THE INVENTION Previously, a series of closely related aminobenzophenones (e. g. 4- (2-amino-4- nitrophenylamino) benzophenone) have been described (Hussein, F. A. et al, Iraqi J. Sci., 22, 54-66 (1981)). However, there is no description of their uses. WO 98/32730 discloses aminobenzophenone inhibitors of interleukin 1 (3 (IL-1 (3) and tumour necrosis factor a (TNF-a) secretion in vitro, said compounds being potentially useful for treatment of inflammatory diseases in which the production of cytokines is involved in the pathogenesis, e. g. asthma, rheumatoid arthritis, psoriasis, contact dermatitis, and atopic dermatitis. Furthermore the compounds of PCT/DK98/00008 were tested in vivo for anti- inflammatory properties in the 12-0-tetradecanoylphorbol-13-acetate (TPA) induced murine chronic skin inflammation model, (De Young, L. M. et al., Agents Actions, 26, 335-341 (1989) ; Carlson, R. P. et al., Agents Actions, 17, 197-204 (1985) ; Alford, J. G. et al., Agents Action, 37, (1992) ; Stanley, P. L. et al., Skin Pharmacol, 4, 262-271 (1991)). In this chronic skin inflammation model the compounds had the same potency compared to the reference compound hydrocortisone.

The purpose of the present invention is to provide further pharmacologically active benzophenone derivatives and related compounds.

It has surprisingly been found that novel aminobenzophenone derivatives according to the general formula I are potent inhibitors of interleukin 1 ß (IL-1 3) and tumour necrosis factor a (TNF-a) secretion in vitro, making them potentially useful for treatment of inflammatory diseases, in which the secretion and regulation of cytokines or more specifically interleukin 1 ß (IL-1 3) and tumour necrosis factor a (TNF-a) are involved in the pathogenesis. The inhibition or down regulation of the cytokines is possibly due to an inhibition of MAP kinases. The preparation of structurally related aminobenzophenones useful as dyes for textiles is disclosed in Man-Made Text. India (1987), 30 (6), 275-6 ; Man-Made Text. India (1986), 29 (5), 224-30 ; and Man-Made Text. India (1985), 28 (11), 425, 427-9, 431 ; and a structurally related aminobenzophenone is disclosed in JP 81-61259 as a reactant in the preparation of fluoran color formers.

SUMMARY OF THE INVENTION The compounds of the present invention are represented by the general formula I

wherein R1 represents a substituent selected from the group consisting of halogen, hydroxy, mercapto, trifluoromethyl, amino, (C1-C3) alkyl, (C2-C3) olefinic group, (Cl-C3) alkoxy, (C1-C3) alkylthio, (C1- C6) alkylamino, (C1-C3) alkoxycarbonyl, cyano,-CONH2, phenyl, or nitro ; R2 represents one or more, same or different substituents selected from the group consisting of hydrogen, halogen, hydroxy, mercapto, trifluoromethyl, amino, (Cl-C3) alkyl, (C2-C3) olefinic group, (C1- C3) alkoxy, (C1-C3) alkylthio, (C1-C6) alkylamino, (C1-C3) alkoxycarbonyl, cyano,-CONH2, phenyl, or nitro ; R3 represents one or more, same or different substituents selected from the group consisting of hydrogen, halogen, hydroxy, mercapto, trifluoromethyl, cyano, carboxy, carbamoyl, (C1-C10) alkyl, (C2- C1 ) olefinic group, (C3-C8) monocyclic hydrocarbon group, (C1-C10)alkoxy, (C1-C10)alkylthio, (C1- C10) alkoxycarbonyl, or phenyl ; R4 represents hydrogen, (Cl-C6) alkyl, (C2-C6) olefinic group, or (C3-C6) monocyclic hydrocarbon group ; R5 represents one or more, same or different substituents selected from the group consisting of hydrogen and R1 ; X represents oxygen, sulphur, or N-OH ; with the proviso that when X represents oxygen then R1, R2 and R5 together does not represent more than 8 fluorine substituents and with the proviso that the following compounds are not included in formula I : 2-Chloro-4'- (2-chlorophenylamino) benzophenone,

2-Chloro-4'-(phenylamino)benzophenone, 2-Hydroxy-4'- (phenylamino) benzophenone, 2-Hydroxy-4'- (4-hydroxyphenylamino) benzophenone, 2-Hydroxy-4'- (4-methoxyphenylamino) benzophenone, 2-Hydroxy-4'- (2-hydroxyphenylamino) benzophenone, 2-Hydroxy-4'- (2-methoxyphenylamino) benzophenone, 2-Methoxy-4'-(2-methoxyphenylamino) benzophenone, and 2-Methyl-4'- (4-methoxyphenylamino) benzophenone.

DETAILED DESCRIPTION OF THE INVENTION Preferred embodiments of the invention In compounds of formula I R1 preferably represents a substituent selected from the group consisting of fluoro, chloro, bromo, hydroxy, trifluoromethyl, amino, (C1-C2) alkyl, (C2-C3) alkenyl, (C1-C3) alkoxy, (C1-C3) alkoxycarbonyl, cyano, and-CONH2 ; R2 represents one or more, same or different substituents selected from the group consisting of hydrogen, fluoro, chloro, bromo, hydroxy, trifluoromethyl, amino, (C1-C3) alkyl, (C2-C3) alkenyl, and (Cl- C3) alkoxy.

R3 represents one or more, same or different substituents selected from the group consisting of hydrogen, fluoro, chloro, bromo, hydroxy, trifluoromethyl, (C1-C6) alkyl, (C2-C6) alkenyl, (C1-C6) alkoxy, (C1-C6) alkoxycarbonyl, cyano, carboxy, and-CONH2.

R4 represents hydrogen, (C1-C4) alkyl, or (C2-C4) olefinic group ; X represents oxygen or sulphur ; R5 represents one or more, same or different substituents selected from the group consisting of hydrogen, fluoro, chloro, bromo, hydroxy, trifluoromethyl, amino, (C1-C2) alkyl, (C2-C3) alkenyl, (C1- C3) alkoxy, (C1-C3) alkoxycarbonyl, cyano, and-CONH2 ; More preferably R1 represents a substituent selected from the group consisting of fluoro, chloro, bromo, hydroxy, methyl, and methoxy ;

R2 represents one or more, same cr different substituents selected from the group consisting of hydrogen, fluoro, chloro, bromo, hydroxy, methyl, and methoxy ; R3 represents one or more, same or different substituents selected from the group consisting of hydrogen, fluoro, chloro, bromo, hydroxy, methyl, methoxy, cyano, and carboxy ; R4 represents hydrogen, methyl, or ethyl ; R5 represents one or more, same or different substituents selected from the group consisting of hydrogen, fluoro, chloro, bromo, hydroxy, trifluoromethyl, methyl, ethyl, and methoxy ; X represents oxygen ; The phenyl group of R1, R2, R3, and R5 may optionally be substituted, e. g. with hydroxy ; amino ; nitro ; cyano ; halogen, preferably fluoro, chloro, or bromo ; methyl ; or methoxy.

A preferred embodiment of the invention is the formula VII : wherein X, R1, R2, R3, R4, and R5 have the meanings specified above except that R2 does not represent hydrogen. Preferred compounds of formula VII are compounds wherein R2 represents a halogen atom, preferably chlorine.

Specific compounds of formula I or VII of the invention are : 2-[[3-Chloro-4-(2-methylbenzoyl)] phenylamino] benzonitrile (Compound 101), 2-Chloro-2'-methyl-4- (2-methyl-phenylamino) benzophenone (Compound 102), 2-Chloro-2'-methyl-4- (phenylamino) benzophenone (Compound 103), 2-Chloro-4-(2-methoxy-phenylamino)-2'-methylbenzophenone (Compound 104), 2-Chloro-4-(2-fluoro-phenylamino)-2'-methylbenzophenone (Compound 105), 2-Chloro-4-(2-chloro-phenylamino)-2'-methylbenzophenone (Compound 106), 4-(2-tert-Butyoxy-phenylamino)-2-chloro-2'-methylbenzophenon e (Compound 107), 2-Chloro-4- (2-hydroxy-phenylamino)-2'-methylbenzophenone (Compound 108), 2-Chloro-4- (3-chloro-phenylamino)-2'-methylbenzophenone (Compound 109), 2-Chloro-4- (2- [1, 1, 1-trifluoromethyl]-phenylamino)-2'-methylbenzophenone (Compound 110),

4- (4-Bromo-2, 5-difiuoro-phenylamino)-2-chloro-2'-methylbenzophenone (Compound 111), 2-Chloro-4-(2-ethyl-phenylamino)-2'-methylbenzophenone (Compound 112), 2-Chloro-4-(3-[1, 1, 1-trifluoromethyl] phenylamino)-2'-methylbenzophenone (Compound 113), 2-Chloro-2'-methyl-4-(2-phenyl-phenylamino) benzophenone (Compound 114), 2-Chloro-2'-methyl-4- (3-phenyl-phenylamino) benzophenone (Compound 115), 2-Chloro-4- (4-f I uoro-2-methyl-phenylamino)-2'-methyibenzophenone (Compound 116), 2-Chloro-2'-methyl-4- (3-methyl-phenylamino) benzophenone (Compound 117), 2-Chloro-4- (3-methoxy-phenylamino)-2'-methylbenzophenone (Compound 118), 2-Chloro-4- (4-chloro-phenylamino)-2'-methylbenzophenone (Compound 119), 2-Chloro-2'-methyl-4- (4-phenyl-phenylamino) benzophenone (Compound 120), 4- (4-Bromo-phenylamino)-2-chloro-2'-methylbenzophenone (Compound 121), 4- (4-Bromo-3-fluoro-phenylamino)-2-chloro-2'-methylbenzophenon e (Compound 122), 4- (2-Bromo-phenylamino)-2-chloro-2'-methylbenzophenone (Compound 123), 2-Chloro-4- (4-chloro-2-methyl-phenylamino)-2'-methylbenzophenone (Compound 124), 2-Chloro-4- (4-chloro-3-fluoro-phenylamino)-2'-methylbenzophenone (Compound 125), 2-Chloro-4- (3-fluoro-phenylamino)-2'-methylbenzophenone (Compound 126), 2-Chloro-4- (3, 5-difluoro-phenylamino)-2'-methylbenzophenone (Compound 127), 4- (3-Bromo-phenylamino)-2-chloro-2'-methylbenzophenone (Compound 128), 2-Chloro-4- (3, 4-difluoro-phenylamino)-2'-methylbenzophenone (Compound 129), 2-Chloro-4- (5-fluoro-2-methyl-phenylamino)-2'-methylbenzophenone (Compound 130), 2-Chloro-4- (3-fluoro-2-methyl-phenylamino)-2'-methylbenzophenone (Compound 131), Ethyl 2-[[3-chloro-4-(2-methylbenzoyl)]phenylamino] benzoate (Compound 132), 2-Chloro-3'-fluoro-4- (4-fluoro-2-methyl-phenylamino)-2'-methylbenzophenone (Compound 133), 2-[[3-Chloro-4-(2-methylbanzoyl)]phenylamino]benzoic acid (Compound 134), 2-Chloro-4- (4-fluoro-2-methyl-N-methyl-phenylamino)-2'-methylbenzopheno ne (Compound 135), 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro-2'-methylbenzophenone (Compound 136), 4- (4-Bromo-2-chloro-phenylamino)- 2-chloro-2'-methylbenzophenone (Compound 137), 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro-4'-methoxy-2'-methylbenzophenone (Compound 138), 4- (4-Bromo-2-methyl-phenylamino)- 2, 4'-dichloro-2'-methylbenzophenone (Compound 139), 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro-4'-fluoro-2'-methylbenzophenone (Compound 140), 4- (4-Bromo-2-methyl-phenylamino)- 2-fluoro-2'-methylbenzophenone (Compound 141), 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro--2', 5'-dimethyl-benzophenone (Compound 142), 2-Chloro-4- (4-cyano-2-methyl-phenylamino)-2'-methylbenzophenone (Compound 143), 4-(4-Bromo-2-methyl-N-ethyl-phenylamino)-2-chloro-2'-methylb enzophenone (Compound 144), 2-Chloro-4- (4-bromo-2-methyl-phenylamino)-4'-ethoxy-2'-methylbenzopheno ne (Compound 145), 2, 3'-Dichloro-4- (4-bromo-2-methyl-phenylamino)-2'-methylbenzophenone (Compound 146), and salts thereof with pharmaceutical acceptable acids, hydrates and solvates.

Compounds of formula la wherein X=S and wherein R1, R2, R3, R4, and R5 have the meanings specified for formula 1, and compounds of formula lb wherein X=N-OH and wherein R1, R2, R3, R4, and R5 have the meanings specified for formula I are also generally preferred

Specific compounds of formula la are : 2-[[3-Chloro-4-(2-methyl (thiobenzoyl))] phenylamino] benzonitrile (Compound 301), 2-Chloro-2'-methyl-4- (2-methyl-phenylamino) (thiobenzophenone) (Compound 302), 2-Chloro-2'-methyl-4- (phenylamino) (thiobenzophenone) (Compound 303), 2-Chloro-4-(2-methoxy-phenylamino)-2'-methyl(thiobenzophenon e) (Compound 304), 2-Chloro-4-(2fluoro-phenylamino)-2'-methyl (thiobenzophenone) (Compound 305), 2-Chloro-4-(2-chloro-phenylamino)-2'-methyl(thiobenzophenone ) (Compound 306), 4- (2-tert-Butyoxy-phenylamino)-2-chloro-2'-methyl (thiobenzophenone) (Compound 307), 2-Chloro-4-(3-chloro-phenylamino)-2'-methyl(thiobenzophenone ) (Compound 308), 2-Chloror-4-(3-chloro-phenylamino)-2'-methyl(thiobenzophenon e) (Compound 309), 2-Chloro-4- (2- [1, 1, 1-trifluoromethyl]-phenylamino)-2'-methyl (thiobenzophenone) (Compound 310), 4- (4-Bromo-2, 5-difluoro-phenylamino)-2-chloro-2'-methyl (thiobenzophenone) (Compound 311), 2-Chloro-4-(2-ethyl-phenylamino)-2'-methyl (thiobenzophenone) (Compound 312), 2-Chloro-4- (3- [1, 1, 1-trfluoromethyl]phenylamino)-2'-methyl(thiobenzophenone) (Compound 313), 2-Chloro-2'-methyl-4-(2-phneyl-phenylamino)(thiobenzopenone) (Compound 314), 2-Chloro-2'-methyl-4- (3-phenyl-phenylamino) (thiobenzophenone) (Compound 315), 2-Chloro-4-(4-fluoro-2-methyl-phenylamino)-2'-methyl(thioenz ophenone) (Compound 316), 2-Chloro-2'-methyl-4-(3-methyl-phenylamino)(thiobenzophenone ) (Compound 317), 2-Chloro-4-(3-methoxy-phenylamino)-2'-methyl(thiobenzophenon e)(Compound 318), 2-Chloro-4- (4-chloro-phenylamino)-2'-methyl (thiobenzophenone) (Compound 319), 2-Chloro-2'-methyl-4-(4-phenyl-phenylamino) (thiobenzophenone) (Compound 320), 4- (4-Bromo-phenylamino)-2-chloro-2'-methyl (thiobenzophenone) (Compound 321), 4- (4-Bromo-3-fluoro-phenylamino)-2-chloro-2'-methyl (thiobenzophenone) (Compound 322), 4-(2-Bromo-phenylamino)-2-chloro-2'-methyl(thiobenzophenone) (Compound 323), 2-Chloro-4-(4-chloro-2-methyl-phenylamino)-2'-methyl(thioben zophenone) (Compound 324), 2-Chloro-4- (4-chloro-3-fluoro-phenylamino)-2'-methyl (thiobenzophenone) (Compound 325), 2-Chloro-4-(3-fiuoro-phenylamino)-2'-methyl (thiobenzophenone) (Compound 326), 2-Chloro-4- (3, 5-difluoro-phenylamino)-2'-methyl (thiobenzophenone) (Compound 327), 4- (3-Bromo-phenylamino)-2-chloro-2'-methyl (thiobenzophenone) (Compound 328), 2-Chloro-4- (3, 4-difluoro-phenylamino)-2'-methyl (thiobenzophenone) (Compound 329),

2-Chloro-4- (5-fluoro-2-methyl-phenylamino)-2'-methyl (thiobenzophenone) (Compound 330), 2-Chloro-4- (3-fluoro-2-methyl-phenylamino)-2'-methyl (thiobenzophenone) (Compound 331), Ethyl 2-[[3-chloro-4-(2-methyl (thiobenzoyl))] phenylamino] benzoate (Compound 332), 2-Chloro-3'-fluoro-4- (4-fluoro-2-methyl-phenylamino)-2'-methyl (thiobenzophenone) (Compound 333), 2-[[3-Chloro-4-(2-methyl(thiobenzoyl))]phenylamino]benzoic acid (Compound 334), 2-Chloro-4- (4-fluoro-2-methyl-N-methyl-phenylamino)-2'-methyl (thiobenzophenone) (Compound 335), 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro-2'-methyl (thiobenzophenone) (Compound 336), 4- (4-Bromo-2-chloro-phenylamino)- 2-chloro-2'-methyl (thiobenzophenone) (Compound 337), 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro-4'-methoxy-2'-methyl (thiobenzophenone) (Compound 338), 4- (4-Bromo-2-methyl-phenylamino)- 2, 4'-dichloro-2'-methyl (thiobenzophenone) (Compound 339), 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro-4'-fluoro-2'-methyl (thiobenzophenone) (Compound 340), 4- (4-Bromo-2-methyl-phenylamino)- 2-fluoro-2'-methyl (thiobenzophenone) (Compound 341), 4- (4-Bromo-2-methyl-phenylamino)-2-chloro--2', 5'-dimethyl- (thiobenzophenone) (Compound 342), 2-Chloro-4-(4-cyano-2-methyl-phenylamino)-2'-methyl(thiobenz ophenone) (Compound 343), 4- (4-Bromo-2-methyl-N-ethyl-phenylamino)-2-chloro-2'-methyl (thiobenzophenone) (Compound 344), 2-Chloro-4- (4-bromo-2-methyl-phenylamino)-4'-ethoxy-2'-methyl (thiobenzophenone) (Compound 345), 2, 3'-Dichloro-4- (4-bromo-2-methyl-phenylamino)-2'-methyl (thiobenzophenone) (Compound 346), and salts thereof with pharmaceutically acceptable acids, hydrates and solvates.

Specific compounds of formula lb are : 2-[[3-Chloro-4-[(hydroxyimino)(2-methylphenyl)methyl]]phenyl amino]benzonitrile (Compound 401), 2-Chloro-2'-methyl-4-(2-methyl-phenylamino)benzophenone oxime (Compound 402), 2-Chloro-2'-methyl-4- (phenylamino) benzophenone oxime (Compound 403), 2-Chloro-4-(2-methoxy-phenylamino)-2'-methylbanzophenone oxime (Compound 404), 2-Chloro-4-(2-fluoro-phenylamino)-2'-methylbenzophenone oxime (Compound 405), 2-Chloro-4- (2-chloro-phenylamino)-2'-methylbenzophenone oxime (Compound 406), 4-(2-tert-Butyoxy-phenylamino)2-chloro-2'-methylenzophenone oxime (Compound 407), 2-Chloro-4-(2-hydroxy-phenylamino)-2'-methylbenzophenone oxime (Compound 408), 2-Chloro-4- (3-chloro-phenylamino)-2'-methylbenzophenone oxime (Compound 409), 2-Chloro-4- (2- [1, 1, 1-trifluoromethyl]-phenylamino)-2'-methylbenzophenone oxime (Compound 410), 4- (4-Bromo-2, 5-difluoro-phenylamino)-2-chloro-2'-methylbenzophenone oxime (Compound 411), 2-Chloro-4-(2-ethyl-phenylamino)-2'-methylbanzophenone oxime (Compound 412), 2-Chloro-4- (3- [1, 1, 1-trifluoromethyl]phenylamino)-2'-methylbenzophenone oxime (Compound 413), 2-Chloro-2'-methyl-4- (2-phenyl-phenylamino) benzophenone oxime (Compound 414), 2-Chloro-2'-methyl-4- (3-phenyl-phenylamino) benzophenone oxime (Compound 415), 2-Chloro-4-(4-fluoro-2-methyl-phenylamino)-2'-methylbenzophe none oxime (Compound 416), 2-Chloro-2'-methyl-4- (3-methyl-phenylamino) benzophenone oxime (Compound 417),

2-Chloro-4-(3-methoxy-phenylamin (;)-2'-methylbenzophenone oxime (Compound 418), 2-Chloro-4-(4-chloro-phenylamino)-:''-methylbenzophenone oxime (Compound 419), 2-Chloro-2'-methyl-4- (4-phenyl-phenylamino) benzophenone oxime (Compound 420), 4- (4-Bromo-phenylamino)-2-chloro-2'-methylbenzophenone oxime (Compound 421), 4- (4-Bromo-3-fluoro-phenylamino)-2-chloro-2'-methylbenzophenon e oxime (Compound 422), 4- (2-Bromo-phenylamino)-2-chloro-2'-methylbenzophenone oxime (Compound 423), 2-Chloro-4- (4-chloro-2-methyl-phenylamino)-2'-methylbenzophenone oxime (Compound 424), 2-Chloro-4- (4-chloro-3-fluoro-phenylamino)-2'-methylbenzophenone oxime (Compound 425), 2-Chloro-4- (3-fluoro-phenylamino)-2'-methylbenzophenone oxime (Compound 426), 2-Chloro-4- (3, 5-difluoro-phenylamino)-2'-methylbenzophenone oxime (Compound 427), 4- (3-Bromo-phenylamino)-2-chloro-2'-methylbenzophenone oxime (Compound 428), 2-Chloro-4- (3, 4-difluoro-phenylamino)-2'-methylbenzophenone oxime (Compound 429), 2-Chloro-4- (5-fluoro-2-methyl-phenylamino)-2'-methylbenzophenone oxime (Compound 430), 2-Chloro-4- (3-fluoro-2-methyl-phenylamino)-2'-methylbenzophenone oxime (Compound 431), Ethyl 2-[[3-chloro-4-[(hydroxyimino)(2-methylphenyl)methyl]]phenyl amino] benzoate (Compound 432), 2-Chloro-3'-fluoro-4- (4-fluoro-2-methyl-phenylamino)-2'-methylbenzophenone oxime (Compound 433), 2-[[3-Chloro-4-[(hydroxyimino)(2-methylphenyl)methyl]]phenyl amino] benzoic acid (Compound 434), 2-Chloro-4- (4-fluoro-2-methyl-N-methyl-phenylamino)-2'-methylbenzopheno ne oxime (Compound 435), 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro-2'-methylbenzophenone oxime (Compound 436), 4- (4-Bromo-2-chloro-phenylamino)- 2-chloro-2'-methylbenzophenone oxime (Compound 437), 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro-4'-methoxy-2'-methylbenzophenone oxime (Compound 438), 4- (4-Bromo-2-methyl-phenylamino)- 2, 4'-dichloro-2'-methylbenzophenone oxime (Compound 439), 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro-4'-fluoro-2'-methylbenzophenone oxime (Compound 440), 4- (4-Bromo-2-methyl-phenylamino)- 2-fluoro-2'-methylbenzophenone oxime (Compound 441), 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro--2', 5'-dimethyl-benzophenone oxime (Compound 442), 2-Chloro-4- (4-cyano-2-methyl-phenylamino)-2'-methylbenzophenone oxime (Compound 443), 4- (4-Bromo-2-methyl-N-ethyl-phenylamino)-2-chloro-2'-methylben zophenone oxime (Compound 444), 2-Chloro-4- (4-bromo-2-methyl-phenylamino)-4'-ethoxy-2'-methylbenzopheno ne oxime (Compound 445), 2, 3'-Dichloro-4- (4-bromo-2-methyl-phenylamino)-2'-methylbenzophenone oxime (Compound 446), and salts thereof with pharmaceutical acceptable acids, hydrates and solvates.

The compounds of formulae 1, VII, la, and lb can be used in the form of their salts which are formed with pharmaceutical acceptable inorganic or organic acids, such as hydrochloric, hydrobromic and hydroiodic acid, phosphoric acid, sulphuric acid, nitric acid, p-toluenesulphonic acid, methanesulphonic acid, formic acid, acetic acid, propionic acid, citric acid, tartaric acid, succinic acid, benzoic acid, maleic acid, these examples being considered as non-limiting for the invention.

As used in the specification, unless specified to the contrary, the following terms have the meaning indicated :

"Alkyl"refers to any univalent group derived from an alkane by removal of a hydrogen atom from any carbon atom, and includes the subclasses of normal alkyl (n-alkyl), and primary, secondary and tertiary alkyd groups respectively, and having the number of carbon atoms specified, including for example (C1- <BR> <BR> <BR> C3) alkyl, (C1-C5) alkyl, (C5) alkyl, (C6-C1 ) alkyl, (C6-C 5) alkyl, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, and t-butyl. Alkane refers to an acyclic branched or unbranched hydrocarbon having the general formula CnH2n+2, and therefore consisting entirely of hydrogen atoms and saturated carbon atoms.

"Olefinic group"refers to a straight or branched acyclic hydrocarbon having one or more carbon-carbon double bonds of either E or Z stereochemistry where applicable, and having the number of carbon atoms specified. The term includes, for example, (C2-C15) olefinic group, preferably a (C2-C15) alkenyl ; (C2-C3) olefinic group, preferably a (C2-C3) alkenyl ; vinyl ; allyl ; 1-butenyl ; 2-butenyl ; and 2-methyl-2- propenyl. Olefinic groups having only one carbon-carbon double bond, herein called alkenyl, are preferred.

"Alkoxy'refers broadly to a radical of the formula-OR, where R is alkyl as defined above, for example (cl-c3) alkoxy, (C1-C2) alkoxy, methoxy, ethoxy, n-propoxy, and the like.

"(C1-C3) alkylthio"refers broadly to a radical of the formula-SR, where R is alkyl as defined above and includes methylthio, ethylthio, n-propylthio, and 2-propylthio.

"(C1-C6) alkylamino"refers broadly to a radical of the formula-NHR or-NR2, where R is alkyl as defined above having from 1-6 carbon atoms and includes, for example, methylamino, dimethylamino, di- (n- propyl) amino, and n-butyl (ethyl) amino.

"(C1-C3) alkoxycarbonyl refers broadly to a radical of the formula-COOR, where R is alkyl as defined above and includes methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, and i-propoxycarbonyl.

"(C3-C10) monocyclic hydrocarbon group"includes the saturated cycloalkanes and unsaturated cyclic olefins, such as cycloalkenes having one endocyclic double bond, and having from 3-10 carbon atoms, and includes, for example, (C3-C8) cycloalkyl, cyclopropyl, cyclopentyl, cyclohexyl, and cyclooctyl, (C3- C10) cycloalkene group, and (C3-C8) cycloalkene group. Specific examples are cycloprop-2-enyl, cyclobut-2-enyl, cyclopent-2-enyl, cyclohex-3-enyl, and cyclonon-4-enyl.

"Amino"means the group-NH2.

"Carbamoyl"refers to the group-CONH2,-CONHR, and-CONRR'where R and R'represent alkyl as defined above.

"Carboxy'refers broadly to a radical of the formula-COOH.

"Halogen"means the same or different of fluoro, chloro, bromo, and iodo ; fluoro, chloro, and bromo being preferred.

Pharmacological methods To study the effect of the compound of the present invention in vitro the inhibition of the IL-1 ß and TNF- a secretion was measured using the following procedure : Cytokine production was measured in the media from lipopolysaccharide (LPS) stimulated peripheral blood mononuclear cells. The mononuclear cells were isolated from human peripheral blood by Lymphoprep (Nycomed, Norway) fractionation and suspended in RPMI 1640 (growth medium) with foetal calf serum (FCS, 2%), at a concentration of 5 x 105 cells/ml. The cells were incubated in 24-well tissue culture plates in 1 ml aliquots. Test compounds were dissolved in dimethylsulfoxide (DMSO, 10 mM) and were diluted with the medium. Compounds were added to the cells for 30 minutes, then LPS (1 mg/ml final concentration) was added. The plates were incubated for 18 hours, and the concentration of IL-1 ß and TNF-a in the medium was determined by enzyme-linked immunosorbent assays. The median inhibitory concentrations (IC50) of the compounds were calculated. The results are shown in Table 1.

The compounds of the present invention also show similar activities in the ability to inhibit PMN (polymorphonuclear) superoxide secretion which is also indicative of potentially useful anti-inflammatory drugs. The compounds were tested using the following procedure : Human polymorphonuclear (PMN) granulocytes were isolated from human blood by dextran sedi- mentation, Lymphoprep fractionation and hypotonic lysis of contaminating erythrocytes.

Superoxide anion generation was measured as the superoxide dismutase inhibitable reduction of ferricytochrome C (Madhu, S. B. et al, Inflammation, 16, 241, (1992)). The cells were suspended in Hanks'balanced salt solution, and incubated for 10 minutes at 37°C with test compounds. The cells were primed by the addition of TNF-a (3 ng/ml final concentration) for 10 minutes, and then ferricytochrome C, (final concentration 750pg/ml), bovine serum albumin (BSA, final concentration 1 mg/ml) and formyl-methionyl-leucyl-phenylalanine (fMLP, final concentration 10-7 M) were added for 3 minutes. The cells were chilled on ice, and were spun down. The optical densities in the cell-free supernatant was measured in a spectrophotometer. The median inhibitory concentration (IC50) of the compounds was calculated. The results are shown in Table 1.

Table 1. Inhibition of cytokines and PMN-superoxide production in vitro by compounds of the present invention.

The median inhibition concentration (IC50, nM) of Comp. No. ; IL-1 (3 TNF-a PMN- superoxide 102 13 4. 0 6. 3 105 25 4. 0 13 109 50 7. 9 20 116 32 7. 9 3. 7 119 40 16 5. 0 130 40 6. 3 50 131 13 4. 0 13 136 100 8. 0 100 ref. A) 13 7. 1 5. 0 ref. a) : 4-(2-Aminophenylamino)-2-chloro-2'-methylbenzophenone, compound 106 disclosed in WO 98/32730.

These results show that the compounds of the present invention are able to inhibit the production of IL- 1 ß, TNF-a and PMN-superoxide, and showing a pharmacological activity comparable to a reference compound, thus making them potentially useful in the treatment of inflammatory diseases. It appears from the results shown in Table 1 that some of the compounds of the invention are more selective for one of these inflammatory cytokines than for the other two. This may be an advantage in certain therapeutic situations where a more selective cytokine inihibition is indicated.

To study the compounds of the present invention in vivo the 12-5tetradecanoylphorbol-13-acetate (TPA) induced murine chronic skin inflammation model can be used (De Young, L. M. et al, Agents Actions, 26, 335-341 (1989) ; Carlson, R. P. et al, Agents Actions, 17, 197-204 (1985) ; Alford, J. G. et al, Agents Action, 37, (1992) ; Stanley, P. L. et al, Skin Pharmacol, 4, 262-271 (1991)), cf. description of method in WO 98/32730 hereby incorporated by reference. These results show that the compounds of the present invention are of the same potency compared to known reference compounds, e. g. hydrocortisone with its known side effects, whereas the compounds of the present invention are well tolerated and are non-toxic. Some members of the present class of compounds show a very low systemic absorption, thus making them especially useful in the treatment of various dermatological diseases. In general, they may be administered by e. g. oral, intravenous, intranasal, topically or transdermal routes.

METHOD OF PREPARATION The compounds of the present invention can be prepared in a number of ways well known to those skilled in the art of organic synthesis. The compounds of the present invention can be synthesised using the methods outlined below, together with methods known in the art of synthetic organic chemistry, or variations thereof as appreciated by those skilled in the art. Preferred methods include, but are not limited to, those described below.

The novel compounds of formulae 1, VII, la, and lb may be prepared using the reactions and techniques described in this section. The reactions are performed in solvents appropriate to the reagents and materials employed and are suitable for the transformations being effected. Also, in the synthetic methods described below, it is to be understood that all proposed reaction conditions, including choice of solvent, reaction atmosphere, reaction temperature, duration of experiment and work-up procedures, are chosen to be conditions of standard for that reaction, which should be readily recognised by one skilled in the art. It is understood by one skilled in the art of organic synthesis that the functionality present on various portions of the educt molecule must be compatible with the reagents and reactions proposed. Not all compounds of formula I falling into a given class may be compatible with some of the reaction conditions required in some of the methods described. Such restrictions to the substituents which are compatible with the reaction conditions will be readily apparent to one skilled in the art and alternate methods can be used.

Compounds according to the present invention may be prepared by a process comprising coupling of an amine of the formula III with a bromide, iodide, fluoride, chloride or triflate with the formula 11, as shown in scheme 1, where R1, R2, R3, R4, R5, and X are as defined in general formula 1, except that any substituents or functional groups which are potentially reactive in the coupling reaction may themselves be protected before the coupling reaction is performed and subsequently removed.

The coupling reaction is carried out using any of the methods for the formation of diphenylamines known to one skilled in the art of organic synthesis. The preferred method is the palladium catalysed amination method which comprises coupling of an amine with an arylhalogenide (or aryltriflate) in the presence of a base, a suitable Pd source, and a suitable phosphine ligand in an inert solvent.

The palladium compound used in the process is not particularly limited, and as specific examples are palladium (II) acetate, palladium (II) chloride, palladium (II) bromide, dichlorobis (triphenylphosphine) palladium (II), tetrakis (triphenylphosphine) palladium (0), tris (dibenzylideneacetone) dipalladium (0). The preferred ligands include, but are not limited to, racemic or non-racemic 2, 2'-bis (diphenylphosphino)-1, 1'-binaphthyl (hereinafter refered to as BINAP), tri-o- tolylphosphine, tri-tert-butylphosphine, 1, 1'-bis (diphenylphosphino)-ferrocene, bis [ (2- diphenylphosphino) phenyl] ether (DPEphos), 2-dicyclohexylphosphanyl-2'-dimethylaminobiphenyl, 2- (di- tert-butylphosphino) biphenyl, and 9, 9-dimethyl-4, 6-bis (diphenylphosphino) xanthene (Xantphos). The amount of palladium and ligand used in this process is typically in the range 0. 1 to 10 % by mole relative

to the amount of the aromatic halide (or triflate) used.

Especially sodium-tert-butoxide (NaOt-Bu) and caesium carbonate (Cs2CO3) have proven to be the best bases in this process, but other bases may be used as well.

The reaction is typically performed at elevated temperature (80-120 °C) in inert solvents like 1, 4- dioxane, toluene, benzene and tetrahydrofurane under an inert atmosphere like argon or nitrogen. Ri X R R2 111 Ra "c D/ 5 ho III-f-II Coupling Coupling Ri X R3 fi R5 R I 2 H 4 n e D/ 4 1, (R4=H) Alkylation R-Y-1, (R4 not H) L : Br, I, OSO2CF3, or F and Cl (in special cases) Y : CI, Br, I, OSO2CF3, OSO2CH3, or OTs FGI : Functional group interconversion Scheme 1

Compounds according to the present invention in which R4 is not hydrogen may be prepared by a process comprising coupling of an amine of the formula I (R4= H) with an alkylating agent, as shown in scheme 1, where R1, R2, R3, R5, and X are as defined in general formula 1, except that any substituents or functional group which are potentially reactive in the coupling reaction may themselves be protected before the coupling reaction is performed and subsequently removed.

Typically alkylating agents of the general formula R-Y include, but are not limited to, iodides (Y=I), bromides (Y=Br), chlorides (Y=CI) and sulfonates (L=OSO2R', where R'represents methyl, trifluoromethyl or 4-methylphenyl).

Compounds according to the present invention may in special cases be prepared by a simple functional group interconversion (FGI), meaning a standard process, known to those skilled in the art of organic synthesis, where a functional group in compounds with the general formula I is transformed into a different functional group in one or more synthetic steps, leading to a new compound with the general formula 1. Examples of such processes are, but are not limited to, hydrolysis of an ester to give an acid under basic conditions ; deprotection of a methylether to give a phenol by treatment with e. g. borontribromide (BBr3) ; and catalytic hydrogenation of an olefin to give a saturated hydrocarbon.

Compounds according to the present invention with the general formula I where X = S may be prepared from the ketone (with the general formula 1, C =O) by such an FGI process, by using one of the many thiocarbonylating reagent, known to those skilled in the art of organic synthesis. Examples of such thiocarbonylating reagents include, but are not limited to, phosphorous pentasulfide (P4S10), or Lawesson's reagent (2, 4-bis (4-methoxyphenyl)-1, 3, 2, 4-dithiaphosphetane-2, 4-disulfide) or the like.

Compounds according to the present invention with the general formula I where X = N-OH may be prepared from the ketone (with the general formula 1, C =O) by treatment with hydroxylamine, or a protected derivative thereof followed by deprotection, in an appropriate solvent like e. g. pyridine or methanol.

Compounds according to the present invention with the general formula III may be prepared by several methods known to those skilled in the art of organic synthesis. One useful sequence is shown in scheme 2. The key step comprising coupling of a bromide (or iodide) with the general formula VI with an acid chloride with the general formula V to afford the benzophenone with the general formula IV. This compound IV may then be reduced to the corresponding amine with the general formula III by treatment with standard reducing agents. Examples of such reducing agents include, but are not limited to, stannous chloride dihydrate ; hydrogen, ammonium formiate, or hydrazine hydrate and a catalytic amount of palladium on carbon. The coupling reaction is done by transforming the bromide (VI) into a reactive organometallic intermediate, e. g. by treatment with butyllithium to afford the lithium derivative or by treatment with magnesium to afford the magnesium derivative.

R 1 0 Val vu CW NO2 Vu V 5 R V ! V Coupling Ri X Ri X Reduction R//N02 R//NH2 s R2 s R2 IV (X=O) 111 FG I IV (X=SorX=N-OH) hal : Br, I SCHEME 2 The reactivity of this intermediate is then modulated by transmetalation to e. g. zinc, by treatment with ZnCip, ZnBr2, or Znl2. This organozinc compund is then coupled with the acid chloride, with the general formula V, under the influence of a palladium (0) complex in catalytic amount. Examples of such catalyst include but are not particularly limited to tetrakis (triphenylphosphine) palladium (0), tetrakis (triphenylarsine) palladium (0), dichlorobis (triphenylphosphine) palladium (II), or benzylchlorobis (triphenylphosphine) palladium (ll).

As shown on scheme 2 compounds with the general formula IV (X = O) may be transformed by an FGI process to give compounds with the general formula IV (X = S or X = N-OH) as described above. This is only to illustrate the flexibility in the synthesis and in general the described sequence of processes is only one of many possible strategies for the synthesis of compound of the present invention. That is, it may be more advantageous in some cases to alter the sequence of the processes described above.

The described sequence of processes is not considered as being limited for the preparation of the compounds of the present invention with the general formula I and alteration of the reaction sequence is

an obvious alternative for those skilled in the art of organic synthesis.

The present compounds are intended for use in pharmaceutical compositions which are useful in the treatment of the above mentioned diseases.

The amount required of a compound of formula 1, Viol, lb and la (hereinafter referred to as the active compound or active ingredient) for therapeutic effect will, of course, vary both with the particular compound, the route of administration and the mammal under treatment. A suitable dose of an active compound for systemic treatment is 0. 1 to 200 mg/kg bodyweight, the most preferred dosage being 0. 2 to 50 mg/kg of mammal bodyweight, administered one or more times daily.

While it is possible for an active ingredient to be administered alone as the raw chemical, it is preferable to present it as a pharmaceutical formulation. Conveniently, the active ingredient comprises from 0. 1% to 100% by weight of the formulation. Conveniently, dosage units of a formulation contain between 0. 07 mg and 1 g of the active ingredient. For topical administration, the active ingredient preferably comprises from 1% to 20% by weight of the formulation but the active ingredient may comprise as much as 50% w/w. Formulations suitable for nasal or buccal administration may comprise 0. 1 % to 20% w/w. for example about 2% w/w of active ingredient.

By the term"dosage unit"is meant a unitary, i. e. a single dose which is capable of being administered to a patient, and which may be readily handled and packed, remaining as a physically and chemically stable unit dose comprising either the active material as such or a mixture of it with solid or liquid pharmaceutical diluents or carriers.

The formulations, both for veterinary and human medical use, of the present invention comprise an active ingredient in association with a pharmaceutical acceptable carrier therefore and optionally other therapeutic ingredient (s). The carrier (s) must be"acceptable"in the sense of being compatible with the other ingredients of the formulations and not deleterious to the recipient thereof.

The formulations include those in a form suitable for oral, ophthalmic, rectal, parenteral (including subcutaneous, intramuscular and intravenous), transdermal, intra-articular, topical, nasal, or buccal administration.

The formulations may conveniently be presented in dosage unit form and may be prepared by any of the methods well known in the art of pharmacy. All methods include the step of bringing the active ingredient into association with the carrier which constitutes one or more accessory ingredients. In general, the formulations are prepared by uniformly and intimately bringing the active ingredient into association with a liquid carrier or a finely divided solid carrier or both, and then, if necessary, shaping the product into the desired formulation.

Formulations of the present invention suitable for oral administration may be in the form of discrete units as capsules, sachets, tablets or lozenges, each containing a predetermined amount of the active ingredient ; in the form of a powder or granules ; in the form of a solution or a suspension in an aqueous liquid or non-aqueous liquid ; or in the form of an oil-in-water emulsion or a water-in-oil emulsion. The active ingredient may also be administered in the form of a bolus, electuary or paste.

Formulations for rectal administration may be in the form of a suppository incorporating the active ingredient and a carrier such as cocoa butter, or in the form of an enema.

Formulations suitable for parenteral administration conveniently comprise a sterile oily or aqueous preparation of the active ingredient which is preferably isotonic with the blood of the recipient.

Formulations suitable for intra-articular administration may be in the form of a sterile aqueous prepara- tion of the active ingredient which may be in microcrystalline form, for example, in the form of an aqueous microcrystalline suspension. Liposomal formulations or biodegradable polymer systems may also be used to present the active ingredient for both intra-articular and ophthalmic administration.

Formulations suitable for topical administration, including eye treatment, include liquid or semi-liquid pre- parations such as liniments, lotions, gels, applicants, oil-in-water or water-in-oil emulsions such as creams, ointments or pastes ; or solutions or suspensions such as drops.

Formulations suitable for administration to the nose or buccal cavity include powder, self-propelling and spray formulations, such as aerosols and atomizers.

In addition to the aforementioned ingredients, the formulations of this invention may include one or more additional ingredients.

The compositions may further contain other therapeutically active compounds usually applied in the treatment of the above mentioned pathological conditions, for instance glucocorticoids, vitamin D analogues, anti-histamines, platelet activating factor (PAF) antagonists, anticolinergic agents, methyl xanthines, ß-adrenergic agents, COX-2 inhibitors, salicylates, indomethacin, flufenamate, naproxen, timegadine, gold salts, penicillamine, serum cholesterol-reducing agents, retinoids, zinc salts, and salicylazosulfapyridin (Salazopyrin).

The novel compounds of the invention are of value in the human and veterinary practice as systemic and topical therapeutic agents for the treatment and prevention of diseases. The novei compounds show anti-acne properties and, i. a., anti-inflammatory and cytokine regulating effects possibly due to MAP kinase inhibition, and are useful in the treatment and prophylaxis of asthma, allergy, arthritis, including rheumatoid arthritis and spondyloarthritis, gout, atherosclerosis, chronic inflammatory bowel

disease (Crohn's disease), proliferative and inflammatory skin disorders, such as psoriasis, atopic dermatitis or acne ; uveitis, septic shock, AIDS, and osteoporosis.

The invention will now be further described in the following non-limiting general procedures, preparations and examples.

EXAMPLES General procedures, preparations and Examples Specific examples of compounds of formula I are listed in Table 2.

All melting points are uncorrected. For 1 H and 13C nuclear magnetic resonance (NMR) spectra (300 MHz for 1 H) chemical shift values (8) (in ppm) are quoted, unless otherwise specified, for deuteriochloroform and hexadeuterodimethylsulfoxide solutions relative to internal tetramethylsilane (8 0. 00) or chloroform (1 H NMR 8 7. 25, 13C NMR 8 76. 81). The value for a multiplet (m), either defined (doublet (d), triplet (t), quartet (q)) or not at the approximate mid point is given unless a range is quoted (s singlet, b broad). The organic solvents used were anhydrous. The term"chromatography"refers to column chromatography using the flash technique and was performed on silica gel.

The following abbreviations have been used throughout this specification : BINAP= racemic or non- racemic 2, 2'-bis (diphenylphosphino)-1, 1'-binaphthyl, CDC13=deuteriochloroform, DMSO- d6=hexadeuterodimethylsulfoxide, DMSO=dimethylsulfoxide, EtOAc=ethyl acetate, Et20=diethylether, Pd2 (dba) 3= tris (dibenzylideneacetone) dipalladium (0), THF=tetrahydrofurane, TLC=thin layer chromatography.

Table 2 Compounds of General formula I Comp. No. X R1 R2 R3 R4 R Example No.

101, Ex. 1 O Me 2-Cl 2-CN H H 102, Ex. 2 O Me 2-C1 2-Me H H 103, Ex. 3 O Me 2-Cl H H H 104, Ex. 4 O Me 2-Cl 2-OMe H H 105, Ex. S O Me 2-C1 2-F H H 106, Ex. 6 O Me 2-Cl 2-Cl H H 107, Ex. 7 O Me 2-C1 2-Ot-Bu H H 108, Ex. 8 O Me 2-Cl 2-OH H H 109, Ex. 9 O Me 2-Cl 3-Cl H H 110, Ex. 10 O Me 2-Cl 2-CF3 H H 111, Ex. 110Me2-02, 5-di-F, 4-Br H H 112, Ex. 12 O Me 2-Cl 2-Et H H 113, Ex. 13 O Me 2-Cl 3-CF3 H H 114, Ex. 14 O Me 2-Cl 2-phenyl H H 115, Ex. 15 O Me 2-Cl 3-phenyl H H 116, Ex. 16 O Me 2-Cl 2-Me, 4-F H H 117, Ex. 17 O Me 2-Cl 3-Me H H 118, Ex. 18 O Me 2-Cl 3-OMe H H 119, Ex. 19 O Me 2-Cl 4-Cl H H 120, Ex. 20 O Me 2-Cl 4-phenyl H H 121, Ex. 21 O Me 2-C1 4-Br H H 122, Ex. 22 O Me 2-Cl 3-F, 4-Br H H 123, Ex. 23 O Me 2-Cl 2-Br H H 124, Ex. 24 O Me 2-Cl 2-Me, 4-Cl H H 125, Ex. 25 O Me 2-Cl 3-F, 4-Cl H H Table 2 (continued) Compounds of General formula I Comp. No. X R1 R2 R3 R4 R5 Example No.

126, Ex. 26 O Me 2-Cl 3-F H H 127, Ex. 27 O Me 2-Cl 3,5-di-F H H 128, Ex. 28 o Me 2-Cl 3-Br H H 129, Ex. 29 O Me 2-C1 3, 4-di-F H H 130, Ex. 30 O Me 2-C1 2-Me, 5-F H H 131, Ex. 31 O Me 2-Cl 2-Me, 3-F H H 132, Ex. 32 O Me 2-C1 2-COOEt H H 133, Ex. 33 O Me 2-Cl 2-Me, 3-F H 3-F 134, Ex. 34 O Me 2-C1 2-COOH H H 135, Ex 35 O Me 2-Cl 2-Me, 4-F Me H 136, Ex 36 O Me 2-Cl 2-Me, 4-Br H H 137, Ex 37 O Me 2-C1 2-C1, 4-Br H H 138, Ex 38 O Me 2-Cl 2-Me, 4-Br H 4-OMe 139, Ex 39 O Me 2-Cl 2-Me, 4-Br H 4-Cl 140, Ex 40 O Me 2-Cl 2-Me, 4-Br H 4-F 141, Ex 41 O Me 2-F 2-Me, 4-Br H H 142, Ex 42 O Me 2-Cl 2-Me, 4-Br H 5-Me 143, Ex. 43 O Me 2-Cl 2-Me, 4-CN H H 144, Ex. 44 O Me 2-C1 2-Me, 4-Br Et H 145, Ex. 45 O Me 2-Cl 2-Me, 4-Br H 4-OEt 146, Ex. 46 O Me 2-Cl 2-Me, 4-Br H 3-Cl The numbering in Table 2 refers to the numbering in the formula below

General procedure 1 Coupling of compounds of the general formula 11 with compounds of the general formula III to give compounds of the general formula 1, or a protected derivative thereof.

A Schlenk tube was charged with the base (Cs2CO3 or NaOt-Bu, 1. 4 mmol), Pd2 (dba) 3 (0. 05 mmol), and BINAP (0. 075 mmol). The tube was capped with a rubber septum and flushed with argon for 5 min, then a solution of a halogenide (1. 1 mmol), with the general formula 11, and an amine (1. 0 mmol), with the general formula i ! t, in 1, 4-dioxane or toluene (5. 0 ml) was added via canula. The resulting solution was first stirred under argon at room temperature for 15 min and then at 100 °C for 4-20 h or until the starting materials had disappeared as seen on TLC. The reaction mixture was allowed to cool to room temperature. The reaction mixture was poured into a mixture of EtOAc and water. The organic phase was separated, dried (MgS04), filtered and concentrated in vacuo. The residue was purified either by chromatography and/or crystallization to afford the coupled product with the general formula 1, or a protected derivative thereof.

General procedure 2 Coupling of compounds of the general formula Vi with compounds of the general formula V to give compounds of the general formula IV, or a protected derivative thereof.

The bromide (80 mmol) with the general formula VI was dissolved in dry THF (65 ml) and cooled with stirring to-78 °C under an atmosphere of argon. n-Butyllithium (80 mmol, 1. 6 M solution in hexane) was then added dropwise, keeping the internal temperature below-65 °C and stirring the resulting mixture for further 15 min. A THF solution of ZnCl2 (100 mmol, 1. 0 M) was added dropwise and the reaction mixture was allowed to warm to room temperature. After 2 h the reaction mixture was cooled to 0 °C,

and tetrakis (triphenylphosphine) palladium (0) (4. 0 mmol) was added followed by the dropwise addition of the acid chloride (84 mmol), with the general formula V, in THF. The reaction mixture was allowed to warm to 20 °C and stirred for ca 16 h. The resulting yellow solution, was filtered and the filtrate poured into a mixture of EtOAc/water 1 : 1, shaken and separated. The aqueous phase was extracted with two more portions of EtOAc. The organic phases were combined, dried (MgS04), filtered, and concentrated in vacuo to afford the crude product. Further purification was done by flash chromatography and/or crystallization to give the title compound IV, or a protected derivative thereof.

General procedure 3 Reduction of compounds of the general formula IV with stannous chloride dihydrate to give compounds of the general formula 111, or a protected derivative thereof.

A mixture of a compound with the general formula IV (5 mmol) and stannous chloride dihydrate (5. 64 g, 25 mmol) in absolute ethanol (50 ml) was heated to 70 °C under argon. After 1 hour, or until the starting material had disappeared as seen on TLC, the solution was allowed to cool to room temperature and then poured into ice/water. The pH was made alkaline by the addition of saturated sodium hydroxide (50 ml) before being extracted with ethyl acetate (3x100 ml). The organic phase was dried (MgS04), filtered and evaporated to afford the crude product. The crude product was further purified either by crystallization or flash chromatography to yield the title compound or a protected derivative thereof.

Preparation 1 : 2-Chloro-2'-methyl-4-nitrobenzophenone (Compound 201) General procedure : 2 Starting compound VI : 2-Bromotoluene Starting compound V : 2-Chloro-4-nitro-benzoyl chloride Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDC13) : 8 195. 1, 148. 9, 145. 5, 140. 6, 135. 0, 133. 1, 132. 7, 132. 4, 131. 9, 130. 0, 125. 9, 125. 4, 121. 9, 21. 5 Preparation 2 : 4-Amino-2-chloro-2'-methylbenzophenone (Compound 202)

General procedure : 3 Starting compound IV : 2-Chloro-2'-methyl-4-nitrobenzophenone (Compound 201) Purification : Chromatography using EtOAc/pentane 1 : 9 followed by 1 : 4 as eluant 13c NMR (CDCI3) : 8 196. 7, 150. 5, 139. 5, 137. 6, 135. 1, 133. 9, 131. 2, 130. 7, 129. 5, 127. 5, 125. 3, 116. 0, 112. 2, 20. 3 Preparation 3 : 2-Chloro-3'-fluoro-2'-methyl-4-nitrobenzophenone (Compound 203) General procedure : 2 Starting compound VI : 2-Bromo-3-fluorotoluene Starting compound V : 2-Chloro-4-nitro-benzoyl chloride Purification : Chromatography using EtOAc/pentane 1 : 20 as eluant 13C NMR (CDCI3) : 8 194. 3, 161. 8, 149. 1, 144. 8, 137. 6, 133. 0, 130. 3, 127. 2, 126. 9, 126. 8, 125. 5, 122. 0, 119. 8, 11. 7 Preparation 4 : 4-Amino-2-chloro-3'-fluoro-2'-methylbenzophenone (Compound 204) General procedure : 3 Starting compound IV : 2-Chloro-3'-fluoro-2'-methyl-4-nitrobenzophenone (Compound 203) Purification : Chromatography using EtOAc/pentane 1 : 9 followed by CH2CI2 as eluant 13C NMR (CDC13) : 8 195. 2, 161. 5, 150. 7, 142. 1, 135. 5, 134. 2, 127. 1, 126. 5, 124. 5, 117. 2, 116. 0, 112. 2, 11. 5 Preparation 5 : 2-Chloro-4'-methoxy-2'-methyl-4-nitrobenzophenone (Compound 205) General procedure : 2 Starting compound VI : 2-Bromo-5-methoxytoluene Starting compound V : 2-Chloro-4-nitro-benzoyl chloride Purification : Crystallization from a MeOH/cyclohexane 10 : 1

13C NMR (CDCi3) : 8 193. 3, 163. 3, 148. 6, 146. 3, 144. 3, 135. 5, 132. 4, 129. 6, 127. 5, 125. 3, 121. 9, 118. 1, 110. 9, 55. 5, 22. 4 Preparation 6 : 4-Amino-2-chloro-4'-methoxy-2'-methylbenzophenone (Compound 206) General procedure : 3 Starting compound IV : 2-Chloro-4'-methoxy-2'-methyl-4-nitrobenzophenone (Compound 205) Purification : Filtered through a short column of silica gel 13C NMR (CDCI3) : 6 195. 7, 161. 7, 149. 6, 141. 6, 134. 2, 133. 3, 132. 8, 131. 4, 129. 1, 117. 0, 115. 8, 112. 4, 110. 3, 55. 3, 21. 3 Preparation 7 : 2, 4'-Dichloro-2'-methyl-4-nitrobenzophenone (Compound 207) General procedure : 2 Starting compound VI : 2-Bromo-5-chlorotoluene Starting compound V : 2-Chloro-4-nitro-benzoyl chloride Purification : Chromatography using EtOAc/pentane 1 : 15 followed by 1 : 10 as eluant 13C NMR (CDC13) : 8 194. 1, 149. 0, 145. 0, 142. 6, 139. 4, 133. 5, 133. 1, 132. 7, 132. 5, 130. 1, 126. 1, 125. 5, 122. 0, 21. 4 Preparation 8 : 4-Amino-2, 4'-dichloro-2'-methylbenzophenone (Compound 208) General procedure : 3 Starting compound IV : 2, 4'-Dichloro-2'-methyl-4-nitrobenzophenone (Compound 207) 13C NMR (CDC13) : 8 195. 4, 150. 5, 139. 8, 137. 9, 136. 5, 135. 1, 133. 7, 131. 2, 130. 9, 127. 5, 125. 6, 115. 9, 112. 3, 20. 2 Preparation 9 : 2-Chloro-4'-fluoro-2'-methyl-4-nitrobenzophenone (Compound 209)

General procedure : 2 Starting compound VI : 2-Bromo-5-fluorotoluene Starting compound V : 2-Chloro-4-nitro-benzoyl chloride Purification : Chromatography using EtOAc/pentane 1 : 20 as eluant 13C NMR (CDCI3) : 8 193. 7, 165. 1, 148. 9, 145. 3, 144. 6, 134. 7, 132. 6, 131. 4, 129. 9, 125. 5, 122. 0, 119. 5, 113. 0, 21. 8 Preparation 10 : 4-Amino-2-chloro-4'-fluoro-2'-methylbenzophenone (Compound 210) General procedure : 3 Starting compound IV : 2-Chloro-4'-fluoro-2'-methyl-4-nitrobenzophenone (Compound 209) Purification : Filtered through a short column of silica gel 13C NMR (CDCI3) : 8 195. 4, 163. 9, 150. 3, 141. 5, 135. 5, 134. 9, 133. 5, 132. 2, 128. 0, 118. 1, 115. 9, 112. 4, 112. 3, 20. 6 Preparation 11 : 2-Fluoro-4-nitro-2'-methylbenzophenone (Compound 211) General procedure : 2 Starting compound VI : 2-Bromotoluene Starting compound V : 2-Fluoro-4-nitro-benzoyl chloride Purification : Crystallization from a mixture of MeOH/cyclohexane 6 : 1 13C NMR (CDC13) : 8 193. 1, 159. 9, 150. 3, 139. 3, 136. 4, 133. 8, 132. 6, 132. 1, 131. 7, 130. 8, 125. 8, 119. 4, 112. 4, 21. 0 Preparation 12 : 4-Amino-2-fluoro-2'-methylbenzophenone (Compound 212) General procedure : 3 Starting compound IV : 2-Fluoro-4-nitro-2'-methylbenzophenone (Compound 211) Purification : Filtered through a short column of silica gel

13C NMR (CDC13) : 8 194. 3, 163. 8, 153. 0, 140. 7, 136. 1, 134. 0, 130. 8, 129. 9, 127. 9, 125. 3, 116. 8, 110. 1, 101. 3, 19. 8 Preparation 13 : 2-Chloro-2', 5'-dimethyl-4-nitrobenzophenone (Compound 213) General procedure : 2 Starting compound VI : 2-Bromo-1, 4-dimethylbenzene Starting compound V : 2-Chloro-4-nitro-benzoyl chloride Purification : Filtered through a short column of silica gel 13C NMR (CDC13) : 8 195. 3, 148. 9, 145. 6, 137. 4, 135. 5, 135. 0, 133. 9, 132. 8, 132. 3, 132. 2, 130. 0, 125. 5, 121. 9, 21. 1, 20. 8 Preparation 14 : 4-Amino-2-chloro-2', 5'-dimethylbenzophenone (Compound 214) General procedure : 3 Starting compound IV : 2-Chloro-2', 5'-dimethyl-4-nitrobenzophenone (Compound 213) Purification : Filtered through a short column of silica gel 13C NMR (CDC13) : 8 196. 8, 150. 2, 139. 3, 135. 1, 134. 9, 134. 5, 133. 8, 131. 4, 131. 1, 130. 0, 128. 0, 116. 0, 112. 2, 20. 8, 19. 9 Preparation 15 : 2-Chloro-4'-ethoxy-2'-methyl-4-nitrobenzophenone (Compound 215) General procedure : 2 Starting compound VI : 2-Bromo-5-ethoxytoiuene Starting compound V : 2-Chloro-4-nitro-benzoyl chloride Purification : Crystallization from a mixture of MeOH/cyclohexane 10 : 1 13C NMR (CDC13) : b 193. 3, 162. 8, 148. 5, 146. 4, 144. 3, 135. 5, 132. 4, 129. 5, 127. 3, 125. 3, 121. 9, 118. 5, 111. 2, 63. 8, 22. 5, 14. 6 Preparation 16 : 4-Amino-2-chloro-4'-ethoxy-2'-methylbenzophenone

(Compound 216) General procedure : 3 Starting compound IV : 2-Chloro-4'-ethoxy-2'-methyl-4-nitrobenzophenone Purification : Filtered through a short column of silica gel 13C NMR (CDC13) : 8 195. 7, 161. 2, 149. 6, 141. 7, 134. 2, 133. 4, 132. 7, 131. 1, 129. 2, 117. 5, 115. 7, 112. 4, 110. 8, 63. 5, 21. 4, 14. 7 Preparation 17 : 2, 3'-Dichloro-2'-methyl-4-nitrobenzophenone (Compound 217) General procedure : 2 Starting compound VI : 2-Bromo-3-chlorotoluene Starting compound V : 2-Chloro-4-nitro-benzoyl chloride Purification : Crystallization from a mixture of MeOH/cyclohexane 9 : 1 13C NMR (CDCI3) : 8 194. 6, 149. 2, 144. 5, 138. 2, 137. 3, 137. 0, 133. 5, 133. 2, 130. 7, 129. 0, 126. 5, 125. 7, 122. 0, 17. 3 Preparation 18 : 4-Amino-2, 3'-dichloro-2'-methylbenzophenone (Compound 218) General procedure : 3 Starting compound IV : 2, 3'-Dichloro-2'-methyl-4-nitrobenzophenone Purification : Filtered through a short column of silica gel 13C NMR (CDC13) : 5 195. 3, 150. 9, 142. 4, 135. 8, 135. 8, 134. 8, 134. 6, 131. 0, 126. 8, 126. 7, 126. 4, 116. 2, 112. 2, 17. 1 Example 1 2- [ [3-Chloro-4- (2-methylbenzoyl)] phenylamino] benzonitrile (Compound 101) To a solution of 4-amino-2-chloro-2'-methylbenzophenone (10 mmol) and 2-fluorobenzonitrile (10 mmol) in DMSO (25 ml) was added potassium tert-butoxide (2. 36 g, 21 mmol). The reaction mixture was stirred at room temperature for 40 hours, diluted with water (300 ml) and extracted with ethyl acetate (3x100 ml). The organic phase was dried (MgS04), filtered and concentrated in vacuo to afford the crude product. The crude product was further purified by flash chromatography using EtOAc/pentane

1 : 9 as eluent to yield the title compound, which crystallized after trituration in pentane.

13C NMR (CDC13) : 8 196. 4, 144. 4, 144. 3, 138. 6, 134. 1, 133. 6, 133. 5, 132. 7, 131. 6, 131. 5, 130. 3, 125. 5, 122. 0, 119. 7, 117. 4, 116. 9, 116. 4, 101. 9, 20. 7 Example 2 2-Chloro-2'-methyl-4-(2-methyl-phenylamino) benzophenone (Compound 102) General procedure : 1 Starting compound 11 : 2-Bromotoluene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaOt-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDC13) : 8 196. 5, 149. 0, 139. 4, 138. 1, 137. 8, 135. 2, 133. 7, 132. 3, 131. 4, 131. 2, 130. 7, 129. 6, 128. 4, 127. 1, 125. 4, 125. 3, 123. 8, 115. 8, 112. 2, 20. 4, 17. 9 Example 3 2-Chloro-2'-methyl-4- (phenylamino) benzophenone (Compound 103) General procedure : 1 Starting compound) L bromobenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaOt-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDCI3) : 8 196. 5, 147. 8, 140. 2, 139. 2, 137. 9, 135. 0, 133. 5, 131. 3, 130. 8, 129. 7, 129. 6, 129. 2, 125. 4, 123. 8, 121. 0, 116. 4, 112. 9, 20. 4 Example 4 2-Chloro-4-(2-methoxy-phenylamino)-2'-methylbenzophenone (Compound 104) General procedure : 1 Starting compound II : 2-Bromoanisole Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaOt-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant

13C NMR (CDC13) : 8 196. 4, 149. 9, 147. 3, 139. 2 137. 9, 134. 9, 133. 4, 131. 2, 130. 8, 129. 7, 129. 7, 129. 2, 125. 4, 123. 1, 120. 8, 118. 6, 117. 0, 113. 4, 111. 1, 55. 6, 20. 4 Example 5 2-Chloro-4- (2-fluoro-phenylamino)-2'-methylbenzophenone (Compound 105) General procedure : 1 Starting compound II : 1-Bromo-2-fluorobenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : Toluene Base : Cs2CO3 Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 3C NMR (CDCI3) : # 196. 5, 154. 5, 146. 7, 138. 9, 138. 1, 134. 8, 133. 2, 131. 4, 131. 0, 130. 2, 129. 9, 128. 6, 125. 4, 124. 6, 124. 0, 121. 2, 117. 0, 116. 2, 113. 6, 20. 5 Example 6 2-Chloro-4-(2-chloro-phenylamino)-2'-methylbenzophenone (Compound 106) General procedure : 1 Starting compound II : 1-Bromo-2-chlorobenzene Starting compound III : 4-Amino-2-chioro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaOt-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDC13) : # 196. 4, 146. 1, 138. 7, 138. 3, 137. 5, 134. 7, 133. 1, 131. 4, 131. 1, 130. 9, 130. 2, 130. 0, 127. 7, 125. 4, 124. 6, 123. 5, 119. 5, 118. 0, 114. 6, 20. 6 Example 7 4-(2-tert-Butoxy-phenylamino)-2-chloro-2'-methylbenzophenone (Compound 107) General procedure : 1 Starting compound II : 2-Bromo-1-tert-butoxybenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaOt-Bu Purification : Chromatography using Et2O/pentane 1 : 4 as eluant 13C NMR (CDC 3) : # 196. 4, 147. 1, 145. 9, 139. 1, 138. 0, 135. 0, 134. 9,

133. 5, 131. 3, 130. 8, 129. 7, 129. 4, 125. 4, 123. 5, 123. 4, 122. 5, 118. 8, 116. 7, 113. 3, 80. 3, 29. 0, 20. 5 Example 8 2-Chloro-4- (2-hydroxy-phenylamino)-2'-methylbenzophenone (Compound 108) A solution of 4-(2-tert-butoxy-phenylamino)-2-chloro-2'-methylbenzophenone (Compound 107) (1. 33 g, 3. 4 mmol) in a mixture of CH2Ci2 (5 ml) and trifluoroethanol (20 ml) was cooled to-5 °C under argron.

Trifluoroacetic acid (423 mg, 3. 7 mmol) was added dropvise and the reaction mixture was allowed to come to room temperature over 1 h. After 23 h at room temperature the reaction mixture was poured into saturated NaHCO3 and then extracted with EtOAc and CH2C12. The organic phases was collected, dried (MgS04), filtered, and concentrated in vacuo to give the crude product. This was further purified by flash chromatography using EtOAc/pentane 1 : 4 as eluant.

13C NMR (CDC13) : 8 197. 3, 150. 2, 149. 2, 139. 1, 137. 8, 135. 1, 133. 6, 131. 3, 131. 0, 129. 7, 128. 7, 127. 0, 126. 5, 125. 4, 124. 2, 121. 0, 116. 2, 116. 1, 112. 6, 20. 4 Example 9 2-Chloro-4- (3-chloro-phenylamino)-2'-methylbenzophenone (Compound 109) General procedure : 1 Starting compound If : 1-Bromo-3-chlorobenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaOt-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDCI3) : â 196. 5, 146. 6, 141. 8, 138. 8, 138. 1, 135. 3, 134. 9, 133. 2, 131. 4, 131. 1, 130. 6, 130. 3, 129. 9, 125. 4, 123. 4, 120. 1, 118. 2, 117. 3, 113. 7, 20. 5 Example 10 2-Chloro-4- (2- [1, 1, 1-trifluoromethyl]-phenylamino)-2'-methylbenzophenone (Compound 110) General procedure : 1 Starting compound 11 : 1-Bromo-2- (1, 1, 1-trifluoromethyl) benzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaOt-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant

13C NMR (CDC13) : 8 196. 4, 146. 6, 139. 0, 138. 6, 138. 3, 134. 7, 133. 1, 133. 0, 131. 4, 131. 2, 131. 0, 130. 0, 127. 2, 125. 4, 123. 8, 123. 3, 122. 3, 117. 9, 114. 5, 20. 6 Example 11 4- (4-Bromo-2, 5-difluoro-phenylamino)-2-chloro-2'-methylbenzophenone (Compound 111) General procedure : 1 Starting compound II : 1-iodo-4-bromo-2, 5-difluorobenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaOt-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDC13) : 8 196. 4, 155. 6, 149. 3, 144. 5, 138. 5, 138. 2, 134. 6, 132. 8, 132. 2, 131. 6, 131. 4, 130. 2, 125. 5, 120. 1, 118. 7, 115. 1, 106. 3, 20. 7 Example 12 2-Chloro-4- (2-ethyl-phenylamino)-2'-methylbenzophenone (Compound 112) General procedure : 1 Starting compound II : 2-Bromo-ethylbenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaOt-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDCI3) : 8 196. 4, 149. 5, 139. 4, 138. 6, 137. 8, 137. 5, 135. 2, 133. 7, 131. 2, 130. 7, 129. 5, 128. 2, 127. 0, 125. 9, 125. 3, 124. 7, 115. 6, 112. 0, 24. 4, 20. 4, 14. 3 Example 13 2-Chloro-4- (3- [1, 1, 1-trifluoromethyl] phenylamino)-2'-methylbenzophenone (Compound 113) General procedure : 1 Starting compound ll : 1-Bromo-3- (1, 1, 1-trifluoromethyl) benzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaOt-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDC13) : 8 196. 5, 146. 4, 141. 2, 138. 7, 138. 2, 134. 9, 133. 2, 132. 2, 131. 2, 131. 2, 130. 7, 130. 2, 130. 0, 125. 5, 122. 9, 123. 8, 119. 8, 117. 5, 116. 7, 113. 7, 20. 6

Example 14 2-Chloro-2'-methyl-4-(2-phenyl-phenylamino) benzophenone (Compound 114) General procedure : 1 Starting compound II : 2-Bromobiphenyl Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaOt-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 repeated by chromatography using CH2CI2/pentane 1 : 1 as eluant 13C NMR (CDC13) : 8 196. 4, 148. 1, 139. 1, 138. 4, 138. 0, 137. 2, 135. 0, 134. 6, 133. 5, 131. 3, 131. 2, 130. 8, 129. 7, 129. 3, 129. 2, 128. 9, 128. 4, 127. 8, 125. 3, 124. 2, 121. 6, 116. 5, 113. 0, 20. 5 Example 15 2-Chloro-2'-methyl-4- (3-phenyl-phenylamino) benzophenone (Compound 115) General procedure : 1 Starting compound II : 3-Bromobiphenyl Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaOt-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDCI3) : 8 196. 5, 147. 7, 143. 0, 140. 7, 140. 5, 139. 1, 138. 0, 135. 1, 133. 5, 131. 3, 130. 9, 130. 0, 129. 7, 129. 4, 128. 9, 127. 7, 127. 1, 125. 4, 122. 7, 119. 7, 116. 7, 113. 0, 20. 5 Example 16 2-Chloro-4- (4-fluoro-2-methyl-phenylamino)-2'-methylbenzophenone (Compound 116) General procedure : 1 Starting compound II : 2-Bromo-5-fluorotoluene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : Cs2CO3 Purification : Chromatography using EtOAc/pentane 1 : 4 as eluant 13C NMR (CDCI3) : 8 196. 5, 160. 5, 149. 6, 139. 3, 137. 8, 136. 3, 135. 3, 133. 7, 131. 2, 130. 7, 129. 5, 128. 2, 127. 1, 125. 3, 117. 8, 115. 2, 113. 8, 111. 6, 20. 4, 18. 1

Example 17 2-Chloro-2'-methyl-4- (3-methyl-phenylamino) benzophenone (Compound 117) General procedure : 1 Starting compound II : 3-Bromotoluene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using CH2CI2/pentane 2 : 1 as eluant 13C NMR (CDC13) : 8 196. 5, 148. 0, 140. 1, 139. 6, 139. 2, 137. 9, 135. 1, 133. 5, 131. 3, 130. 8, 129. 6, 129. 4, 129. 0, 125. 4, 124. 7, 121. 8, 118. 1, 116. 4, 112. 9, 21. 5, 20. 4 Example 18 2-Chloro-4- (3-methoxy-phenylamino)-2'-methylbenzophenone (Compound 118) General procedure : 1 Starting compound II : 3-Bromoanisole Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDCI3) : S 196. 5, 160. 8, 147. 5, 141. 5, 139. 1, 137. 9, 135. 0, 133. 4, 131. 3, 130. 9, 130. 4, 129. 7, 129. 4, 125. 4, 116. 8, 113. 3, 113. 1, 108. 9, 106. 7, 55. 3, 20. 5 Example 19 2-Chloro-4- (4-chloro-phenylamino)-2'-methylbenzophenone (Compound 119) General procedure : 1 Starting compound II : 1-Bromo-4-chlorobenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant and then trituration in Et2O/pentane 1 : 1 13C NMR (CDC13) : 8 196. 5, 147. 3, 138. 9, 138. 0, 135. 0, 133. 4, 131. 4, 131. 0, 129. 8, 129. 7, 128. 7, 125. 4, 122. 1, 122. 0, 116. 6, 113. 2, 20. 5

Example 20 2-Chloro-2'-methyl-4- (4-phenyl-phenylamino) benzophenone (Compound 120) General procedure : 1 Starting compound II : 4-Bromobiphenyl Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDC13) : 8 196. 5, 147. 5, 140. 4, 139. 5, 139. 1, 137. 9, 136. 6, 135. 1, 133. 5, 131. 3, 130. 9, 129. 7, 129. 4, 128. 8, 128. 2, 127. 1, 126. 7, 125. 4, 121. 0, 116. 6, 113. 2, 20. 5 Example 21 4- (4-Bromo-phenylamino)-2-chioro-2'-methylbenzophenone (Compound 121) General procedure : 1 Starting compound II : 1-lodo-4-bromobenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDC13) : 8 196. 5, 147. 1, 139. 5, 138. 9, 138. 1, 135. 0, 133. 3, 132. 6, 131. 4, 131. 0, 129. 9, 129. 8, 125. 4, 122. 3, 116. 8, 116. 0, 113. 3, 20. 5 Example 22 4- (4-Bromo-3-fluoro-phenylamino)-2-chloro-2'-methylbenzophenon e (Compound 122) General procedure : 1 Starting compound II : 1-lodo-4-bromo-3-fluorobenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDCI3) : 8 196. 5, 159. 6, 145. 9, 141. 7, 138. 6, 138. 3, 134. 8, 134. 1, 133. 1, 131. 5, 131. 2, 131. 0, 130. 0, 125. 5, 117. 8, 116. 5, 114. 2, 107. 7, 101. 5, 20. 6

Example 23 4- (2-Bromo-phenylamino)-2-chloro-2'-methylbenzophenone (Compound 123) General procedure : 1 Starting compound II : 1-lodo-2-bromobenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDCI3) : 8 196. 4, 146. 2, 138. 7, 138. 2, 134. 7, 133. 4, 133. 1, 131. 4, 131. 1, 130. 9, 130. 0, 128. 3, 125. 4, 124. 0, 119. 8, 118. 0, 115. 3, 114. 6, 20. 6 Example 24 2-Chloro-4- (4-chloro-2-methyl-phenylamino)-2'-methylbenzophenone (Compound 124) General procedure : 1 Starting compound II : 2-Bromo-5-chlorotoluene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDC13) : 8 196. 5, 148. 5, 139. 1, 137. 9, 136. 9, 135. 1, 134. 2, 133. 5, 131. 3, 131. 2, 130. 8, 130. 3, 129. 7, 129. 0, 127. 1, 125. 4, 124. 9, 116. 0, 112. 4, 20. 4, 17. 8 Example 25 2-Chloro-4- (4-chloro-3-fluoro-phenylamino)-2'-methylbenzophenone (Compound 125) General procedure : 1 Starting compound II : 1-Bromo-4-chloro-3-fluorobenzene Starting compound ! ! ! : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDCI3) : 8 196. 6, 158. 6, 146. 1, 140. 9, 138. 6, 138. 2, 134. 8, 133. 1, 131. 5, 131. 2, 130. 8, 130. 0, 125. 5, 117. 6, 116. 2, 114. 0, 108. 0, 20. 6

Example 26 2-Chloro-4-(3-fluoro-phenylamino)-'-methylbenzophenone (Compound 126) General procedure : 1 Starting compound II : 1-Bromo-3-fluorobenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDC13) : S 196. 6, 163. 6, 146. 6, 142. 3, 138. 8, 138. 1, 134. 9, 133. 2, 131. 4, 131. 1, 130. 8, 130. 3, 129. 9, 125. 4, 117. 4, 115. 5, 113. 8, 110. 0, 107. 0, 20. 5 Example 27 2-Chloro-4- (3, 5-difluoro-phenylamino)-2'-methylbenzophenone (Compound 127) General procedure : 1 Starting compound II : 1-Bromo-3, 5-difluorobenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDCI3) : 8 196. 6, 164. 0, 163. 8, 145. 4, 143. 5, 138. 4, 134. 6, 132. 9, 131. 5, 131. 4, 130. 1, 125. 5, 118. 5, 114. 9, 101. 7, 101. 7, 97. 9, 20. 6 Example 28 4- (3-Bromo-phenylamino)-2-chloro-2'-methylbenzophenone (Compound 128) General procedure : 1 Starting compound II : 1-lodo-3-bromobenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDCI3) : S 196. 5, 146. 6, 142. 0, 138. 8, 138. 1, 134. 9, 133. 3, 131. 4, 131. 1, 130. 9, 130. 3, 129. 9, 126. 3, 125. 4, 123. 2, 123. 1, 118. 7, 117. 3, 113. 7, 20. 5

Example 29 2-Chloro-4- (3, 4-difluoro-phenylamino)-2'-methylbenzophenone (Compound 129) General procedure : 1 Starting compound II : 1-Bromo-3, 4-difluorobenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using CH2CI2/pentane 2 : 1 as eluant 13C NMR (CDC13) : 5 196. 5, 147. 2, 138. 8, 138. 1, 135. 0, 133. 3, 131. 4, 131. 1, 130. 1, 129. 9, 125. 4, 118. 2, 117. 9, 117. 1, 116. 6, 113. 1, 110. 6, 20. 5 Example 30 2-Chloro-4- (5-fluoro-2-methyl-phenylamino)-2'-methylbenzophenone (Compound 130) General procedure : 1 Starting compound il : 2-Bromo-4-fluorotoluene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using Et20/pentane 1 : 4 as eluant 13C NMR (CDC13) : 8 196. 5, 161. 6, 147. 6, 139. 7, 139. 0, 138. 0, 135. 0, 133. 4, 132. 1, 131. 3, 131. 0, 129. 8, 129. 7, 126. 2, 125. 4, 116. 9, 113. 2, 111. 1, 108. 8, 20. 5, 17. 2 Example 31 2-Chloro-4- (3-fluoro-2-methyl-phenylamino)-2'-methyibenzophenone (Compound 131) General procedure : 1 Starting compound II : 2-Bromo-6-fluorotoluene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : NaO-t-Bu Purification : Chromatography using Et2O/pentane 1 : 2 as eluant 13C NMR (CDC13) : 6 196. 5, 162. 0, 148. 3, 140. 1, 139. 1, 138. 0, 135. 0, 133. 4, 131. 3, 130. 9, 129. 7, 129. 3, 127. 2, 125. 4, 119. 3, 118. 6, 116. 4, 112. 8, 111. 7, 20. 5, 9. 6

Example 32 Ethyl 2- [ [3-chloro-4- (2-methylbenzoyl)] phenylamino] benzoate (Compound 132) General procedure : 1 Starting compound li : Ethyl 2-bromobenzoate Starting compound 111 : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : Toluene Base : Cs2CO3 Purification : Chromatography usina EtOAc/pentane 1 : 50 as eluant 13C NMR (CDC13) : 8 196. 5, 168. 3, 145. 1, 144. 9, 138. 6, 138. 4, 134. 4, 134. 0, 132. 7, 131. 8, 131. 5, 131. 2, 130. 1, 125. 4, 120. 4, 119. 6, 117. 0, 116. 0, 114. 8, 61. 1, 20. 6, 14. 3 Example 33 2-Chloro-3'-fluoro-4- (4-fluoro-2-methyl-phenylamino)-2'-methylbenzophenone (Compound 133) General procedure : 1 Starting compound II : 2-Bromo-5-fluorotoluene Starting compound III : 4-Amino-2-chloro-3'-fluoro-2'-methylbenzophenone Solvent : Toluene Base : Cs2CO3 Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 13C NMR (CDCI3) : 8 195. 0, 161. 5, 160. 7, 150. 1, 142. 1, 136. 5, 135. 7, 134. 1, 133. 6, 127. 4, 126. 5, 124. 5, 124. 5, 117. 9, 117. 2, 115. 2, 113. 9, 111. 5, 18. 1, 11. 5 Example 34 2-[[3-Chloro-4-(2-methylbenzoyl)]phenylamino] benzoic acid (Compound 134) A solution of 50 mg Ethyl 2-[[3-chloro-4-(2-methylbenzoyl)]phenylamino] benzoate (Compound 132) in methanol (2. 0 ml) was added aqueous NaOH (2N, 0. 5 ml) and then refluxed for 1 h. The reaction mixture was made slightly acidic with aqueous HCI (1 N) and then extracted with EtOAc (3*10 ml). The organic phase was washed with water, brine, then dried (MgS04), filtered, and concentrated in vacuo to afford the pure title compound.

13C NMR (CDC13) : 8 196. 6, 173. 2, 146. 0, 144. 5, 138. 6, 138. 3, 135. 3, 134. 3, 132. 9, 132. 6, 132. 5, 131. 6, 131. 4, 130. 3, 125. 5, 121. 3, 119. 7, 117. 8, 115. 8, 112. 9, 20. 7

Example 35 2-Chloro-4- (4-fluoro-2-methyl-N-methyl-phenylamino)-2'-methylbenzopheno ne (Compound 135) A solution of 2-chloro-4- (4-fluoro-2-methyl-phenylamino)-2'-methylbenzophenone (Compound 116) (105 mg) in N-methyl-2-pyrolidinone (2. 0 ml) was added sodium hydride (14 mg) in one portion under stirring. After 10 min at 0 °C methyl iodide (47 mg) was added and the reaction mixture was stirred for 4 hours at room temperature followed by 18 hours at 100 °C. The reaction mixture was poured into water and extracted with EtOAc. The organic phases were separated, dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by chromatography using a mixture of diethylether/pentane 1 : 4 as eluant to yield the title compound.

13C NMR (CDCI3) : 8 196. 2, 161. 2, 151. 7, 140. 3, 139. 5, 138. 7, 137. 2, 135. 1, 133. 5, 130. 8, 130. 2, 129. 7, 129. 0, 125. 8, 125. 0, 118. 0, 114. 5, 113. 3, 109. 6, 38. 9, 20. 0, 17. 5 Example 36 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro-2'-methylbenzophenone (Compound 136) General procedure : 1 Starting compound II : 5-Bromo-2-iodotoluene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : Toluene Base : Cs2CO3 Purification : Chromatography using Et2O/pentane 1 : 3 followed by 1 : 2 as eluant 13C NMR (CDC13) : 8 196. 6, 148. 5, 139. 1, 137. 8, 137. 5, 135. 1, 134. 5, 134. 0, 133. 6, 131. 2, 130. 8, 130. 0, 129. 6, 128. 7, 125. 4, 125. 1, 117. 9, 116. 0, 112. 4, 20. 4, 17. 8 Example 37 4- (4-Bromo-2-chloro-phenylamino)- 2-chloro-2'-methylbenzophenone (Compound 137) General procedure : 1 Starting compound II : 4-bromo-2-chloro-1-iodobenzene Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : 1, 4-Dioxane Base : Cs2CO3 Purification : Chromatography using EtOAc/pentane 1 : 9 as eluant 3C NMR (CDCI3) : 8 196. 4, 145. 3, 138. 4, 138. 4, 137. 0, 134. 6, 132. 9, 132. 6, 131. 6, 131. 5, 131. 3, 130. 7, 130. 1, 125. 4, 125. 0, 120. 0, 118. 5, 115. 1, 114. 4, 20. 6

Example 38 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro-4'-methoxy-2'-methylbenzophenone (Compound 138) General procedure : 1 Starting compound it : 5-Bromo-2-iodotoluene Starting compound III : 4-Amino-2-chloro-4'-methoxy-2'-methylbenzophenone Solvent : Toluene Base : Cs2CO3 Purification : Chromatography using EtOAc/pentane 1 : 4 as eluant 13C NMR (CDCI3) : 8 195. 5, 161. 9, 147. 5, 141. 9, 137. 8, 134. 2, 134. 0, 133. 9, 133. 6, 132. 4, 131. 0, 130. 5, 130. 0, 124. 4, 117. 5, 117. 1, 116. 1, 112. 9, 110. 4, 55. 3, 21. 5, 17. 8 Example 39 4- (4-Bromo-2-methyl-phenylamino)- 2, 4'-dichloro-2'-methylbenzophenone (Compound 139) General procedure : 1 Starting compound II : 5-Bromo-2-iodotoluene Starting compound III : 4-Amino-2, 4'-dichloro-2'-methylbenzophenone Solvent : Toluene Base : Cs2CO3 Purification : Chromatography using EtOAc/pentane 1 : 3 as eluant 13C NMR (CDCI3) : 8 195. 3, 148. 6, 140. 0, 137. 6, 137. 3, 136. 7, 135. 1, 134. 5, 134. 1, 133. 4, 131. 3, 131. 0, 130. 1, 128. 6, 125. 6, 125. 1, 118. 1, 116. 0, 112. 6, 20. 3, 17. 8 Example 40 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro-4'-fluoro-2'-methylbenzophenone (Compound 140) General procedure : 1 Starting compound II : 5-Bromo-2-iodotoluene Starting compound III : 4-Amino-2-chloro-4'-fluoro-2'-methylbenzophenone Solvent : Toluene Base : Cs2CO3 Purification : Chromatography using EtOAc/pentane 1 : 6 as eluant 13C NMR (CDC13) : # 195. 3, 164. 0, 148. 4, 141. 7, 137. 4, 135. 2, 134. 9, 134. 4, 134. 1, 133. 2, 132. 4, 130. 1, 129. 1, 125. 0, 118. 2, 118. 0, 116. 0, 112. 7, 112. 3, 20. 7, 17. 8

Example 41 4- (4-Bromo-2-methyl-phenylamino)- 2-fluoro-2'-methylbenzophenone (Compound 141) General procedure : 1 Starting compound II : 5-Bromo-2-iodotoluene Starting compound III : 4-Amino-2-fluoro-2'-methylbenzophenone Solvent : Toluene Base : Cs2CO3 Purification : Chromatography using EtOAc/pentane 1 : 6 as eluant 13C NMR (CDCI3) : 8 194. 2, 163. 7, 151. 0, 140. 4, 137. 1, 136. 3, 134. 9, 134. 1, 133. 9, 130. 9, 130. 1, 128. 1, 125. 7, 125. 3, 118. 5, 117. 8, 110. 2, 101. 1, 19. 9, 17. 7 Example 42 4- (4-Bromo-2-methyl-phenylamino)- 2-chloro-2', 5'-dimethyl-benzophenone (Compound 142) General procedure : 1 Starting compound II : 5-Bromo-2-iodotoluene Starting compound III : 4-Amino-2-chloro-2', 5'-dimethyl-benzophenone Solvent : Toluene Base : Cs2CO3 Purification : Chromatography using EtOAc/pentane 1 : 8 as eluant 13C NMR (CDCI3) : # 196. 6, 148. 2, 139. 0, 137. 5, 135. 1, 134. 9, 134. 7, 134. 2, 134. 1, 133. 5, 131. 6, 131. 2, 130. 1, 129. 2, 124. 8, 117. 8, 116. 2, 112. 6, 20. 8, 19. 9, 17. 8 Example 43 2-Chloro-4- (4-cyano-2-methyl-phenylamino)-2'-methylbenzophenone (Compound 143) General procedure : 1 Starting compound li : 4-Bromo-3-methylbenzonitrile Starting compound III : 4-Amino-2-chloro-2'-methylbenzophenone Solvent : Toluene Base : Cs2CO3 Purification : Chromatography using EtOAc/pentane 1 : 3 as eluant 13C NMR (CDC13) : # 196. 4, 145. 0, 143. 8, 138. 5, 138. 2, 134. 8, 134. 5, 132. 8, 132. 2, 131. 6, 131. 4, 131. 4, 130. 2, 128. 1, 125. 5, 119. 5, 119. 2, 117. 4, 116. 0, 105. 1, 20. 7, 17. 7

Example 44 4- (4-Bromo-2-methyl-N-ethyl-phenylamino)-2-chloro-2'-methylben zophenone (Compound 144) A solution of 4- (4-bromo-2-methyl-phenylamino)-2-chloro-2'-methylbenzophenon e (Compound 136) (110 mg) in dry tetrahydrofurane (2. 0 ml) was added sodium hydride (19 mg) in one portion under stirring. After 10 min at room temperature ethyl iodide (124 mg) was added and the reaction mixture was stirred for 18 hours under reflux, then poured into water and extracted with EtOAc.

The organic phases were separated, dried (MgS04), filtered and concentrated in vacuo. The residue was purified by chromatography using a mixture of EtOAc/pentane 1 : 8 as eluant to yield the title compound as an oil.

13C NMR (CDC13) : 8 196. 3, 150. 8, 142. 0, 139. 7, 139. 2, 137. 4, 135. 5, 134. 7, 133. 9, 131. 1, 131. 0, 130. 4, 129. 2, 126. 0, 125. 2, 121. 2, 113. 7, 109. 9, 46. 0, 20. 2, 17. 7, 12. 4 Example 45 2-Chloro-4- (4-bromo-2-methyl-phenylamino)-4'-ethoxy-2'-methylbenzopheno ne (Compound 145) General procedure : 1 Starting compound 11 : 5-Bromo-2-iodotoluene Starting compound III : 4-Amino-2-chloro-4'-ethoxy-2'-methylbenzophenone Solvent : Toluene Base : Cs2CO3 Purification : Chromatography using EtOAc/pentane 1 : 4 as eluant 13C NMR (CDC13) : 8 195. 5, 161. 4, 147. 5, 142. 0, 137. 9, 134. 2, 134. 0, 133. 8, 133. 7, 132. 4, 130. 7, 130. 6, 130. 0, 124. 4, 117. 6, 117. 4, 116. 1, 113. 0, 110. 8, 63. 5, 21. 5, 17. 8, 14. 7 Example 46 2, 3'-Dichloro-4- (4-bromo-2-methyl-phenylamino)-2'-methylbenzophenone (Compound 146) General procedure : 1 Starting compound II : 5-Bromo-2-iodotoluene Starting compound III : 4-Amino-2, 3'-dichloro-2'-methylbenzophenone Solvent : Toluene Base : Cs2CO3 Purification : Chromatography using acetone/toluene 1 : 99 as eluant 13C NMR (CDC13) : 8 195. 2, 149. 1, 142. 1, 137. 1, 135. 9, 135. 8, 134. 9, 134. 7, 134. 3, 134. 1, 131. 1, 130. 1, 127. 7, 126. 8, 126. 4, 125. 5, 118. 4, 116. 1, 112. 3, 17. 8, 17. 1

Example 47 Tablet containing compound 102 Compound 102 (active substance) 50 mg Lactose 125 mg Starch 12 mg Methyl cellulose 2 mg Sodium carboxymethyl cellulose 10 mg Magnesium stearate 1 mg The active substance, lactose and starch are mixed to a homogeneous state in a suitable mixer and moistened with a 5 per cent aqueous solution of methyl cellulose 15 cps. The mixing is continued until granules are formed. If necessary, the wet granulation is passed through a suitable screen and dried to a water content of less than 1 % in a suitable drier, e. g. fluid bed or drying oven. The dried granules are passed through a 1 mm screen and mixed to a homogeneous state with sodium carboxymethyl cellulose. Magnesium stearate is added, and the mixing is continued for a short period of time. Tablets with a weight of 200 mg are produced from the granulation by means of a suitable tabletting machine.

Example 48 : Formulation for injection containing compound 102.

Compound 102 (active substance) 1 % Sodium chloride q. s.

Ethanol 10% Water for injection to make 100% The active substance is dissolved in ethanol (10%) then water for injection made isotonic with sodium chloride is added to make 100%. The mixture is filled into ampoules and sterilized.

Example 49 Cream formulation containing compound 102 Compound 102 (10 g) was dissolved in Octyldodecyl myristate (250g) to form Part A. Methylparaben (1 g) and propylparaben (0. 2 g) were dissolved in phenoxyethanol (6 g) and mixed with a 0. 025 M Phosphate buffer pH = 7. 5 (632, 8 g) to form Part B. Cetostearyl alcohol (50 g) and ARLACEL 165 (50 g) was melted in a vessel at 70° to 80 °C. Part A was added and heated to 60-70°C. The aqueous phase was likewise heated to 60-70 °C and slowly added to the melted oil phase under high speed stirring. The homogenized components were cooled to room temperature.