发明名称 1-[(indol-3-yl)carbonyl]piperazine derivatives
摘要 1-[(indol-3-yl)carbonyl]piperazine derivatives of formula (I) and pharmaceutically acceptable salts thereof are disclosed, wherein R represents 1-4 substituents independently selected from H, (C1-4)alkyl (optionally substituted with halogen), (C 1-4)alkyloxy (optionally substituted with halogen), halogen, OH, NH2, CN and NO2; R1 is (C5-8)cycloalkyl or (C5-8)cycloalkenyl; R2 is H, methyl or ethyl; R3, R3', R4, R4', R5, R5' and R6' are independently hydrogen or (C1-4)alkyl, optionally substituted with (C1-4)alkyloxy, halogen or OH; R6 is hydrogen or (C1-4)alkyl, optionally substituted with (C1-4)alkyloxy, halogen or OH; or R6 forms together with R7 a 4-7 membered saturated heterocyclic ring, optionally containing a further heteroatom selected from O and S; or R7 is H, (C1-4)alkyl or (C3-5)cycloalkyl, the alkyl groups being optionally substituted with OH, halogen or (C1-4)alkyloxy. A pharmaceutical compositions comprising these 1-[(indol-3-yl)carbonyl]piperazine derivatives, and the use of these derivatives in the treatment of pain, such as peri-operative pain, chronic pain neuropathic pain, cancer pain, and pain and spasticity associated with multiple sclerosis is also disclosed.
申请公布号 NZ537143(A) 申请公布日期 2005.05.27
申请号 NZ20030537143 申请日期 2003.06.13
申请人 AKZO NOBEL N 发明人 COWLEY, PHILLIP MARTIN;CAULFIELD, WILSON;TIERNEY, JASON;CAIRNS, JAMES;ADAM-WORRALL, JULIA;YORK, MARK
分类号 A61K31/405;A61K31/496;A61K31/4985;A61P1/08;A61P1/14;A61P9/00;A61P11/00;A61P25/00;A61P25/04;A61P25/06;A61P25/08;A61P25/20;A61P25/22;A61P25/28;A61P27/06;A61P29/00;A61P29/02;A61P37/08;C07D209/12;C07D209/42;C07D403/06;C07D471/04;C07D487/04;(IPC1-7):C07D403/06 主分类号 A61K31/405
代理机构 代理人
主权项
地址