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公开(公告)号:EP1292564A2
公开(公告)日:2003-03-19
申请号:EP01906332.0
申请日:2001-02-26
发明人: TANIGUCHI, K.,c/o Fujisawa Pharmaceutical Co. Ltd , KAYAKIRI, H.,c/o Fujisawa Pharmaceutical Co. Ltd , SAKURAI, M.,c/o Fujisawa Pharmaceutical Co. Ltd. , FUJII, Naoakic/o Fujisawa Pharmaceutical Co. Ltd. , WASHIZUKA, K.,c/o Fujisawa Pharmaceutical Co. Ltd , HAMASHIMA, H.,c/o Fujisawa Pharmaceutical Co. Ltd , TOMISHIMA, Y.,c/oFujisawa Pharmaceutical Co. Ltd , HAMADA, K.,c/oFujisawa Pharmaceutical Co. Ltd , YAMAMOTO, N.,c/o Fujisawa Pharmaceutical Co. Ltd , ISHIKAWA, H.,c/o Fujisawa Pharmaceutical Co. Ltd , UNAMI, N.c/o Fujisawa Pharmaceutical Co. Ltd. , MIURA, T.,c/o Fujisawa Pharmaceutical Co. Ltd.
IPC分类号: C07C217/86 , A61K31/133 , A61P11/04 , C07C217/30 , C07D471/04 , C07C311/18 , C07C217/70
CPC分类号: C07D209/08 , C07C217/32 , C07C217/34 , C07C217/70 , C07C217/86 , C07C225/16 , C07C229/34 , C07C229/38 , C07C237/30 , C07C271/28 , C07C311/08 , C07C311/21 , C07D209/88 , C07D213/65 , Y02P20/55
摘要: A compound of the formula (I) wherein X1 is bond or -O(CH2)m- (in which m is an integral number of 1, 2 or 3); X2 is bond, -(CH2)n-, etc. (in which n is an integral number of 1, 2 or 3); R1 is hydrogen or amino protective group; R2 is hydroxy(lower)alkyl or (lower)alkoxy(lower)alkyl; A is phenyl, pyridyl, indolyl or carbazolyl, each of which may be substituted with one or two substituent(s) selected from the group consisting of halogen, hydroxy, lower alkyl, etc.; and B is phenyl or pyridyl, each of which may be substituted with one or two substituent(s) selected from the group consisting of halogen, hydroxy, nitro, etc.; and a pharmaceutically acceptable salt thereof which is useful as a medicament.
摘要翻译: 其中X1是键或-O(CH2)m-(其中m是1,2或3的整数)的式(I)化合物; X2是键, - (CH2)n-等(其中n是1,2或3的整数)。 R1是氢或氨基保护基; R2是羟基(低级)烷基或(低级)烷氧基(低级)烷基; A是苯基,吡啶基,吲哚基或咔唑基,它们各自可以被一个或两个选自卤素,羟基,低级烷基等的取代基取代; 和B是苯基或吡啶基,其中的每一个可以被一个或两个选自卤素,羟基,硝基等的取代基取代; 及其药学上可接受的盐,其可用作药物。