发明授权
- 专利标题: Quinoline-3-carboxamides
- 专利标题(中): 喹啉-3-甲酰胺
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申请号: US766487申请日: 1977-02-07
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公开(公告)号: US4107310A公开(公告)日: 1978-08-15
- 发明人: Andre Allais , Francois Clemence , Roger Deraedt , Odile Le Martret
- 申请人: Andre Allais , Francois Clemence , Roger Deraedt , 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: FRX7603754 19760211
- 主分类号: C07D215/06
- IPC分类号: C07D215/06 ; A61K31/47 ; A61K31/495 ; A61K31/54 ; A61P25/04 ; C07D215/54 ; C07D215/56 ; C07D401/12 ; C07D417/12 ; C07F3/02 ; C07D215/20
摘要:
Novel quinoline-3-carboxamides of the formula ##STR1## wherein R.sub.1 is in the 5,6,7 or 8-position and is selected from the group consisting of hydrogen, halogen, --CF.sub.3, --OCF.sub.3, --SCF.sub.3, straight chain alkyl of 1 to 4 carbon atoms, branched alkyl of 3 to 5 carbon atoms and alkoxy of 1 to 4 carbon atoms, R.sub.2 is selected from the group consisting of hydrogen and methyl, R.sub.3 is selected from the group consisting of thiazolyl, 4,5-dihydrothiazolyl, pyridinyl, oxazolyl and imidazolyl and R.sub.4 is selected from the group consisting of hydrogen, hydroxyl, alkyl of 1 to 4 carbon atoms, phenyl and benzyl with the proviso that when R.sub.1 is in the 7 or 8-position and is halogen, --CH.sub.3, --OCF.sub.3 or --SCF.sub.3 and R.sub.4 is hydrogen, R.sub.3 is not thiazolyl, pyridinyl or oxazolyl and the non-toxic, pharmaceutically acceptable acid addition salts when R.sub.3 is imidazolyl or 4,5-dihydrothiazolyl having analgesic activity and their preparation and novel intermediates therefore.
公开/授权文献
- US5925578A Method for forming fine patterns of a semiconductor device 公开/授权日:1999-07-20
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