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    QUINOXALINEDIONES
    2.
    发明公开
    QUINOXALINEDIONES 失效

    公开(公告)号：EP0885212A1

    公开(公告)日：1998-12-23

    申请号：EP97908156.0

    申请日：1997-02-27

    申请人： Pfizer Research and Development Company, N.V./S.A.

    发明人： BULL, David, John ,  CARR, Christopher, Lee ,  FRAY, Michael, Jonathan ,  GAUTIER, Elisabeth, Colette, Louise ,  MOWBRAY, Charles, Eric ,  STOBIE, Alan

    IPC分类号： A61K31 ,  A61P25 ,  A61P43 ,  C07D241 ,  C07D401 ,  C07D403 ,  C07D409 ,  C07D413 ,  C07D417 ,  C07D521

    CPC分类号： C07D231/12 ,  C07D233/56 ,  C07D249/08 ,  C07D401/04 ,  C07D401/14 ,  C07D403/04 ,  C07D403/14 ,  C07D409/14 ,  C07D413/14 ,  C07D417/14

    摘要： The invention provides compounds of formula (I) and the pharmaceutically acceptable salts thereof, wherein R is a 5-membered ring heteroaryl group containing 3 or 4 nitrogen heteroatoms which is linked to the quinoxalinedione ring by a ring carbon or nitrogen atom, or is a 6-membered ring heteroaryl group containing from 1 to 3 nitrogen heteroatoms which is linked to the quinoxalinedione ring by a ring carbon atom, either of said groups being optionally benzo-fused and optionally substituted, including in the benzo-fused portion, by 1 or 2 substituents each independently selected from C1-C4 alkyl, C2-C4 alkenyl, C3-C7 cycloalkyl, halo, hydroxy, C1-C4 alkoxy, C3-C7 cycloalkyloxy, -COOH, C1-C4 alkoxycarbonyl, -CONR?3R4, -NR3R4¿, -S(O)¿p?(C1-C4 alkyl), -SO2NR?3R4¿, aryl, aryloxy, aryl(C¿1?-C4)alkoxy and het, said C1-C4 alkyl being optionally substituted by C3-C7 cycloalkyl, halo, hydroxy, C1-C4 alkoxy, halo(C1-C4)alkoxy, C3-C7 cycloalkyloxy, C3-C7 cycloalkyl(C1-C4)alkoxy, -COOH, C1-C4 alkoxycarbonyl, -CONR?3R4, -NR3R4¿, -S(O)¿p?(C1-C4 alkyl), -SO2(aryl), -SO2NR?3R4¿, morpholino, aryl, aryloxy, aryl(C¿1?-C4)alkoxy or het, and said C2-C4 alkenyl being optionally substituted by aryl; R?1 and R2¿ are each independently selected from H, fluoro, chloro, bromo, C¿1?-C4 alkyl and halo(C1-C4)alkyl; R?3 and R4¿ are either each independently selected from H and C¿1?-C4 alkyl or, when taken together, are C5-C7 alkylene; p is 0, 1 or 2; together with the preparation of, compositions containing, the uses of and intermediates used in the synthesis of, such compounds. The compounds are useful as NMDA receptor antagonists for treating acute neurodegenerative and chronic neurological disorders.

    摘要翻译： 本发明提供式（I）化合物及其药学上可接受的盐，其中R为含有3或4个氮杂原子的5元环杂芳基，其通过环碳或氮原子与喹喔啉二酮环连接，或为 含有1至3个氮杂原子的6元环杂芳基基团，其通过环碳原子与喹喔啉二酮环连接，所述基团中的任一个任选被苯并稠合并且任选被取代，包括在苯并稠合部分中被1或 2个各自独立选自C 1 -C 4烷基，C 2 -C 4烯基，C 3 -C 7环烷基，卤素，羟基，C 1 -C 4烷氧基，C 3 -C 7环烷氧基，-COOH，C 1 -C 4烷氧基羰基，-CONR 3 R 4，-NR 3 R 4 （C 1 -C 4烷基）， - SO 2 NR 3 R 4，芳基，芳氧基，芳基（C 1 -C 4）烷氧基和het，所述C 1 -C 4烷基任选被C 3 （C 1 -C 4）烷氧基，C 3 -C 7环烷氧基，C 3 -C 7环烷基（C 1 -C 4）烷氧基，-COOH，C 1 -C 4卤代烷基， 烷氧基羰基，-CONR 3 R 4，-NR 3 R 4，-S（O） - ，（C 1 -C 4烷基），-SO 2（芳基），-SO 2 NR 3 R 4，吗啉代，芳基，芳氧基， -C4）烷氧基或het，并且所述C2-C4烯基任选被芳基取代; R 1和R 2各自独立地选自H，氟，氯，溴，C 1 -C 4烷基和卤代（C 1 -C 4）烷基; R 3和R 4'各自独立地选自H和C 1 -C 4烷基，或者当合在一起时为C 5 -C 7亚烷基; p是0,1或2; 以及含有这些化合物的合成中所使用的中间体和用途的组合物的制备。 该化合物可用作治疗急性神经变性和慢性神经疾病的NMDA受体拮抗剂。