发明名称 Phenyl- and pyridinyl derivatives
摘要 A compound of formula I where: R is hydrogen, (C1-7)alkyl, (C1-7)alkoxy, halogen or trifluoromethyl; R1 is hydrogen or halogen, with the proviso that R1 in 4-position is not bromine or iodine; or R and R1 may be together - CH=CH-CH=CH-; R2 is hydrogen, halogen, trifluoromethyl, (C1-7)alkoxy or cyano, with the proviso that R2 is not hydrogen, if X is -C(O)O-; R3 is independently from each other hydrogen, (C1-7)alkyl or form a cycloalkyl group; R4 is hydrogen, halogen, (C1-C7)alkyl, (C1-C7)-alkoxy, -N(R5)2, -N(R5)S(O)2-(C1-C7)-alkyl, -N(R5)C(O)R5 or is a cyclic tertiary amine selected from the group consisting of pyrrol-1-yl, imidazol-1-yl, piperidin-1-yl, piperazin-1-yl, morpholin-4- yl, thiomorpholin-4-yl, 1-oxo-thiomorpholin-4-yl or 1,1-dioxo-thiomorpholin-4-yl, which may be substituted or unsubstituted by substituents as disclosed. R5 is independently from each other hydrogen, C3-6-cycloalkyl, benzyl, or (C1-C7)alkyl; X is -C(O)N(R5)-, -(CH2)mO-, -(CH2)mN(R5)-, -N(R5)C(O)-, -C(O)O- or -N(R5)(CH2)m; Y is -(CH2)n, -O-, -S-, -SO2-, -C(O)- or N(R5') and R5' is C3-6-cycloaklyl, benzyl or (C1-C7)-alkyl; Z is =N-, -CH= or C(Cl)= n is 0 to 4; and m is 1 or 2. A process for preparing a compound of formula I is disclosed. The use of a compound of formula I for treating various diseases is also disclosed, for example migraine, rheumatoid arthritis, asthma, pain, Alzheimer's disease, Parkinson's disease, cardiovascular change, inflammatory diseases of the gut, depression, anxiety, psychosis, motion sickness, anti-emetic.
申请公布号 NZ513322(A) 申请公布日期 2004.07.30
申请号 NZ20000513322 申请日期 2000.02.15
申请人 F 发明人 GALLEY, GUIDO;GODEL, THIERRY;HOFFMANN, TORSTEN;HUNKELER, WALTER;SCHNIDER, PATRICK;STADLER, HEINZ;BOES, MICHAEL
分类号 C07C211/44;A61K31/167;A61K31/44;A61P25/00;A61P29/00;C07C211/54;C07C233/29;C07C233/33;C07C233/44;C07C317/14;C07C317/40;C07C323/41;C07D213/75;C07D213/79;C07D213/81;C07D295/12;C07D295/135;C07D401/04;(IPC1-7):C07D213/00;A61P25/24;A61P25/18;A61P25/16;A61P43/00 主分类号 C07C211/44
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