发明名称 (3-CYCLOALKYL-2, 3, 4, 5 - TETRAHYDRO-1H-BENZO [d] AZEPIN-7-YLOXY) DERIVATIVES, USE THEREOF FOR INHIBITING H3 RECEPTORS, PHARMACEUTICAL COMPOSITION AND PREPARATION METHOD
摘要 FIELD: chemistry. ^ SUBSTANCE: present invention relates to benzazepin derivatives of formula (I), where R1 is unsubstituted cyclobutyl, R2 is 3-pyrazinyl, substituted CON(H)(Me) or 2-pyridinyl-M-pyrrolidinyl, where the said pyrrolidinyl group is substituted with a =O group; which is: methylamide 5-(3-cyclobutyl-2,3,4,5-tetrahydro-1H-benzo[d]azepin-7-yloxy) pyrazine-2-carboxylic acid ^ or 1-{6-[(3-cyclbutyl-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl)oxy]-3-pyridinyl}-2-pyrrolidinone ^ EFFECT: obtaining compounds which have affinity to histamine H3 receptor and pharmaceutical compositons containing said compounds. ^ 11 cl, 288 ex
申请公布号 RU2388752(C2) 申请公布日期 2010.05.10
申请号 RU20050122932 申请日期 2003.12.18
申请人 GLEHKSO GRUP LIMITED 发明人 BAMFORD MARK DZHEJMS;DIN DEHVID KENNET;SEKHMI SANDZHIT SINGKH;UILSON DEHVID MEHTT'JU;VIZERINGTON DZHEJSON
分类号 A61K31/55;A61P25/00;C07D223/16;C07D401/12;C07D401/14;C07D403/12;C07D403/14;C07D405/14;C07D409/12;C07D409/14;C07D413/14;C07D417/12;C07D417/14;C07D471/04;C07D491/04 主分类号 A61K31/55
代理机构 代理人
主权项
地址