Piperazine derivatives inhibiting human immunodeficiency virus replication
    6.
    发明授权
    Piperazine derivatives inhibiting human immunodeficiency virus replication 失效
    哌嗪衍生物抑制人体免疫缺陷病毒复制

    公开(公告)号:US06531476B1

    公开(公告)日:2003-03-11

    申请号:US09720921

    申请日:2001-03-20

    IPC分类号: A61K31495

    CPC分类号: C07D241/04

    摘要: The invention concerns the use of a piperazine derivative of formula (I) wherein: A and B=C═O, C═S or CR7R8 with R7=H, methyl, cyano, cyanomethyl, CO2CH3 or (C═O)CH3 and R8=H or phenyl; R1 to R6=H, OH, or C1-C5 alkoxy; X represents: either C═O, O(C═O), O(C═S), O(SO2), NH(C═O), NH(C═S), NH(SO2), S(C═O) or S(C═S), then Y=NR9R10, CR9R10R11 in which R9, R10 and R11=H, C1-C5 alkyl, C2-C5 alkenyl, or C2-C5 alkynyl or Y=nitrogenous heterocycle comprising 5 to 10 atoms; or X represents O, S, O(C═O)O, NH(C═O)O, or S(C═O)O, then Y=CR9R10R11 with R9, R10, R11 as above; or one of its pharmaceutically acceptable salts for preparing a medicine inhibiting HIV. The invention is useful for treating HIV infection.

    摘要翻译: 本发明涉及式(I)的哌嗪衍生物,其中:A和B = C = O,C = S或CR 7 R 8,其中R 7 = H,甲基,氰基,氰基甲基,CO 2 CH 3或(C = O) = H或苯基; R1至R6 = H,OH或C1-C5烷氧基; X表示C = O,O(C = O),O(C = S),O(SO 2),NH(C = O),NH(C = S) O)或S(C = S),则Y = NR 9 R 10,CR 9 R 10 R 11,其中R 9,R 10和R 11 = H,C 1 -C 5烷基,C 2 -C 5烯基或C 2 -C 5炔基或Y =含氮杂环, 原子 或X表示O,S,O(C = O)O,NH(C = O)O或S(C = O)O),然后Y = CR 9 R 10 R 11,其中R 9,R 10,R 11如上; 或其药学上可接受的盐之一,用于制备抑制HIV的药物。 本发明可用于治疗HIV感染。