发明授权
US4299831A 2-Trifluoromethyl-3-quinoline carboxamides, analgesic and
anti-inflammatory compositions and methods employing them
失效
2-三氟甲基-3-喹啉羧酰胺,止痛剂和抗炎组合物和使用它们的方法
- 专利标题: 2-Trifluoromethyl-3-quinoline carboxamides, analgesic and anti-inflammatory compositions and methods employing them
- 专利标题(中): 2-三氟甲基-3-喹啉羧酰胺,止痛剂和抗炎组合物和使用它们的方法
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申请号: US097711申请日: 1979-11-27
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公开(公告)号: US4299831A公开(公告)日: 1981-11-10
- 发明人: Francois Clemence , Roger Deraedt , Andre Allais , Odile Le Martret
- 申请人: Francois Clemence , Roger Deraedt , Andre Allais , Odile Le Martret
- 申请人地址: FRX Paris
- 专利权人: Roussel Uclaf
- 当前专利权人: Roussel Uclaf
- 当前专利权人地址: FRX Paris
- 优先权: FRX7834592 19781208
- 主分类号: C07D413/12
- IPC分类号: C07D413/12 ; A61K31/47 ; A61K31/505 ; A61P25/04 ; A61P29/00 ; C07D215/56 ; C07D401/12 ; C07D417/12
摘要:
Novel 3-quinoline carboxamides of the formula ##STR1## wherein X' is in the 5,6,7 or 8-position and is selected from the group consisting of hydrogen, halogen, straight or branched alkyl and alkoxy of 1 to 5 carbon atoms, --CF.sub.3, --SCF.sub.3 and --OCF.sub.3, R.sub.1 is selected from the group consisting of hydrogen and alkyl of 1 to 4 carbon atoms, R.sub.2 ' is selected from the group consisting of thiazolyl, 4,5-dihydrothiazolyl, pyridinyl, oxazolyl, isoxazolyl, imidazolyl, pyrimidyl and tetrazolyl, all optionally substituted with alkyl of 1 to 4 carbon atoms and phenyl optionally substituted with at least one member of the group consisting of alkyl and alkoxy of 1 to 4 carbon atoms, --CF.sub.3, --NO.sub.2 and halogen and their non-toxic, pharmaceutically acceptable acid addition salts having analgesic and anti-inflammatory activity and novel intermediates and process for their preparation.
公开/授权文献
- USD413774S Shovel 公开/授权日:1999-09-14
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