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    (1-AZINONE) -SUBSTITUTED PYRIDOINDOLES AS MCH ANTAGONISTS
    3.
    发明公开
    (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

    公开(公告)号：EP2240481A1

    公开(公告)日：2010-10-20

    申请号：EP09700411.3

    申请日：2009-01-09

    申请人： Albany Molecular Research, Inc.

    发明人： GUZZO, Peter ,  SURMAN, Matthew David ,  HENDERSON, Alan John ,  JIANG, May Xiaowu ,  HADDEN, Mark ,  GRABOWSKI, James

    IPC分类号： C07D471/04 ,  C07D521/00 ,  A61K31/437 ,  A61P25/22 ,  A61P25/24

    CPC分类号： C07D471/04 ,  C07D519/00 ,  C07D521/00

    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.