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    Indole, azaindole and related heterocyclic amidopiperazine derivatives
    3.
    发明授权
    Indole, azaindole and related heterocyclic amidopiperazine derivatives 有权
    吲哚，氮杂吲哚和相关的杂环酰胺基哌嗪衍生物

    公开(公告)号：US06825201B2

    公开(公告)日：2004-11-30

    申请号：US10127256

    申请日：2002-04-22

    申请人： Tao Wang ,  Owen B. Wallace ,  Nicholas A. Meanwell ,  Zhongxing Zhang ,  John A. Bender ,  John F. Kadow ,  Kap-Sun Yeung

    发明人： Tao Wang ,  Owen B. Wallace ,  Nicholas A. Meanwell ,  Zhongxing Zhang ,  John A. Bender ,  John F. Kadow ,  Kap-Sun Yeung

    IPC分类号： A61K31496

    CPC分类号： C07D333/24 ,  C07D209/08 ,  C07D209/18 ,  C07D209/20 ,  C07D209/42 ,  C07D231/56 ,  C07D307/80 ,  C07D307/81 ,  C07D403/04 ,  C07D471/04

    摘要： The invention comprises substituted indole, azaindole and related heterocyclic amidopiperazine derivatives of general Formula I wherein: Q is —may represent a bond; A is selected from the group consisting of C1-6alkoxy, C1-6alkyl, C3-7cycloalkyl, phenyl, and heteroaryl; wherein said heteroaryl may be monocyclic or bicyclic and may be comprised of three to eleven atoms selected from the group consisting of C, N, NR9, O, and S, and wherein each ring of said phenyl and heteroaryl is optionally substituted with one to five same or different substituents selected from the group consisting of R19-R23; T is U is NR7, O, or S; V is C(H)kR1, O or N(R7′)k; W is CR3 or NR10; X is CR4 or NR10; Y is CR5 or NR10; Z is CR6 or NR10; k is 0 or 1; and m, n, and p are each independently 0, 1, or 2 provided that the sum of m, n, and p must equal 1 or 2; compositions thereof and their use as antiviral agents, particularly for treating HIV infection.

    摘要翻译： 本发明包括取代的吲哚，氮杂吲哚和通式I的相关杂环酰胺基哌嗪衍生物，其中Q可以表示键; A选自C1-6烷氧基，C1-6烷基，C3-7环烷基，苯基和杂芳基; 其中所述杂芳基可以是单环或双环的，并且可以由选自C，N，NR 9，O和S的三至十一个原子组成，并且其中所述苯基和杂芳基的每个环任选被 一至五个相同或不同的选自R 19 -R 23的取代基; T是U是NR 7，O或S; V是C（H）k R 1，O或N （R 7'）k; W是CR 3或NR 10; X是CR 4或NR 10; Y是CR 5或NR 10; Z是CR 6 >或NR 10; k为0或1; m，n和p各自独立地为0,1或2，条件是m，n和p之和必须等于1或2;其组成及其组成 用作抗病毒剂，特别是用于治疗HIV感染。