发明授权
EP1423117B1 2-SUBSTITUTED 1-ARYLPIPERAZINES AS TACHYKININ ANTAGONISTS AND/OR SEROTONIN REUPTAKE INHIBITORS
有权
2-取代的1-芳基哌嗪作为速激肽拮抗剂和/或血清素再摄取抑制剂
- 专利标题: 2-SUBSTITUTED 1-ARYLPIPERAZINES AS TACHYKININ ANTAGONISTS AND/OR SEROTONIN REUPTAKE INHIBITORS
- 专利标题(中): 2-取代的1-芳基哌嗪作为速激肽拮抗剂和/或血清素再摄取抑制剂
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申请号: EP02794786.0申请日: 2002-08-13
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公开(公告)号: EP1423117B1公开(公告)日: 2005-10-19
- 发明人: ALVARO, Giuseppe, GlaxoSmithKline SpA , JACK, Torquil Iain Maclean, GlaxoSmithKline , TRANQUILLINI, Maria Elvira, GlaxoSmithKline SpA
- 申请人: GLAXO GROUP LIMITED
- 申请人地址: Glaxo Wellcome House Berkeley Avenue Greenford, Middlesex UB6 ONN GB
- 专利权人: GLAXO GROUP LIMITED
- 当前专利权人: GLAXO GROUP LIMITED
- 当前专利权人地址: Glaxo Wellcome House Berkeley Avenue Greenford, Middlesex UB6 ONN GB
- 代理机构: Giddings, Peter John
- 优先权: GB0119797 20010814
- 国际公布: WO2003015784 20030227
- 主分类号: A61K31/495
- IPC分类号: A61K31/495 ; C07D241/04 ; A61P25/24
摘要:
The present invention relates to piperazine derivatives of formula (I), wherein R represents halogen, C1-4 alkyl, trifluoromethoxy or trifluoromethyl; R1 is trifluoromethyl, C1-4 alkyl, C1-4 alkoxy, halogen or trifluoromethoxy; R2 is hydrogen, C1-4alkyl or C2-6alkenyl; R3 represents hydrogen or C1-4alkyl; n and m are independently 0 or an integer from 1 to 3; and pharmaceutically acceptable salts and solvates thereof, process for their preparation and their use in the treatment of condition mediated by tachykinins and/or by selective inhibition of the serotonin reuptake transporter protein.
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