发明公开
EP2240481A1 (1-AZINONE) -SUBSTITUTED PYRIDOINDOLES AS MCH ANTAGONISTS
审中-公开
(1-AZINON) - 取代的吡啶并吲哚AS MCH拮抗剂
- 专利标题: (1-AZINONE) -SUBSTITUTED PYRIDOINDOLES AS MCH ANTAGONISTS
- 专利标题(中): (1-AZINON) - 取代的吡啶并吲哚AS MCH拮抗剂
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申请号: EP09700411.3申请日: 2009-01-09
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公开(公告)号: EP2240481A1公开(公告)日: 2010-10-20
- 发明人: GUZZO, Peter , SURMAN, Matthew David , HENDERSON, Alan John , JIANG, May Xiaowu , HADDEN, Mark , GRABOWSKI, James
- 申请人: Albany Molecular Research, Inc.
- 申请人地址: 30 Corporate Circle Albany, New York 12203 US
- 专利权人: Albany Molecular Research, Inc.
- 当前专利权人: Albany Molecular Research, Inc.
- 当前专利权人地址: 30 Corporate Circle Albany, New York 12203 US
- 代理机构: Adamson Jones
- 优先权: US20530 20080111; US48677 20080429
- 国际公布: WO2009089482 20090716
- 主分类号: C07D471/04
- IPC分类号: C07D471/04 ; C07D521/00 ; A61K31/437 ; A61P25/22 ; A61P25/24
摘要:
Substituted pyridoindoles for incorporation in pharmaceutical compositions employed in the treatment of various diseases correspond to formula (I) wherein R 1 is H or optionally substituted alkyl; R 2 , R 3 , R 4 are each independently selected from H, -O-alkyl, -S-alkyl, alkyl, halo, -CF 3 , and -CN; G is -CR 12 R 13 -NR 5 - or -NR 5 -CR 12 R 13 ; R 5 is H, optionally substituted alkyl, optionally substituted heterocycle, -C(=O)-R 6 , -C(=O)-O-R 7 , or -C(=O)-NR 19 R 20 ; R 6 and R 7 are each optionally substituted alkyl or optionally substituted heterocycle; R 8 , R 9 , R 10 , R 11 , R 12 , R 13 , R 19 and R 20 are each independently selected from H or optionally substituted alkyl; R 14 and R 15 are each independently H or halogen; Y is CH or N; L is -CH 2 -O-, -CH 2 CH 2 -, -CH=CH- or a bond; and B is aryl or heteroaryl or cycloalkyl; with the proviso that, when L is a direct bond, B cannot be unsubstituted heteroaryl or heteroaryl monosubstituted with fluorine.
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