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ANTI-VIRAL AROMATIC O-ALKYLATED OXIMES, ETHERS AND THIOETHERS

机译:抗病毒芳香族O-烷基化的氧,醚和硫醚

摘要

Compounds of the formula(see formula I)wherein Q is (see formula II) or -XR' ;X is oxygen or sulphur;R1 is hydrogen, halogen, C1-C4 alkyl or C1-C4 alkoxy;R2 is hydrogen, halogen, C1-C4 alkyl, C1-C4 alkoxy,C3-C4 alkenyloxy, C3-C4 alkynyloxy, mono-, di- or tri-halomethyl, trifuluoromethoxy, C1-C4 alkylthio, C3-C4branched alkylthio, nitro, or cyano;R3 is hydrogen or C1-C4 alkyl;R 4 is C3-C6 alkenyl, C3-C6 alkynyl, C1-C8 haloalkyl,C1-C8 alkoxyalkyl, C1-C8 alkylthioalkyl, C1-C8 hydroxyalkyl,C1-C8 acyloxyalkyl, C1-C8 aroyloxyalkyl, C1-C8 carboxyalkyl,C1-C8 alkylcarboxyalkyl, C6-C12 arylcarboxyalkyl, C1-C8aminoalkyl, C1-C8 alkylaminoalkyl, C1-C8 dialkylaminoalkyl,C1-C8 trialkylsilylalkyl, wherein each of theaforementioned alkyl moieties may be straight-chain orbranched; C3-C8 cycloalkyl, C1-C6 alkylphenyl, C7-C12arylalkyl, C7-C12 alkarylalkyl, or heterocyclylalkyl,wherein the heterocyclic moiety is morpholinyl,piperidinyl, pyrrolidinyl, piperazinyl, oxiranyl,oxetanyl, furanyl, tetrahydropyranyl ortetrahydrofuranyl;R' is C1-C8 haloalkyl, C1-C8 alkoxyalkyl, C1-C8alkylthioalkyl, C1-C8 hydroxyalkyl, C1-C8 acyloxyalkyl,C1-C8 aroyloxyalkyl, C1-C8 aminoalkyl, C1-C8alkylaminoalkyl, C1-C8 dialkylaminoalkyl, C1-C8trialkylsilylalkyl, wherein each of the aforementionedalkyl moieties may be straight-chain or branched; C1-C6alkylphenyl, C7-C12 arylalkyl, C7-C12 alkarylalkyl, orheterocyclylalkyl, wherein the heterocyclic moiety ismorpholinyl, piperidinyl, pyrrolidinyl, piperazinyl,oxiranyl, oxetanyl, furanyl, tetrahydropyranyl ortetrahydrofuranyl;R5 is hydrogen, halo, methyl, mono-, di- ortri-halomethyl; andR6 is an aliphatic or cyclic side chain as definedherein.These compounds are useful for inhibiting the growthor replication of retroviruses such as HIV.
机译:式的化合物(参见公式I)其中Q是(参见式II)或-XR';X是氧或硫;R1是氢,卤素,C1-C4烷基或C1-C4烷氧基;R2是氢,卤素,C1-C4烷基,C1-C4烷氧基,C 3 -C 4烯氧基,C 3 -C 4炔氧基,单,二或三-卤代甲基,三氟甲氧基,C1-C4烷硫基,C3-C4支链的烷硫基,硝基或氰基;R3是氢或C1-C4烷基;R 4是C3-C6烯基,C3-C6炔基,C1-C8卤代烷基,C 1 -C 8烷氧基烷基,C 1 -C 8烷硫基烷基,C 1 -C 8羟烷基,C1-C8酰氧基烷基,C1-C8芳酰氧基烷基,C1-C8羧烷基,C1-C8烷基羧基烷基,C6-C12芳基羧基烷基,C1-C8氨基烷基,C1-C8烷基氨基烷基,C1-C8二烷基氨基烷基,C1-C8三烷基甲硅烷基烷基,其中每个前述烷基部分可以是直链或分支C3-C8环烷基,C1-C6烷基苯基,C7-C12芳基烷基,C7-C12烷芳基烷基或杂环基烷基,其中杂环部分是吗啉基,哌啶基,吡咯烷基,哌嗪基,环氧乙烷基,氧杂环丁烷基,呋喃基,四氢吡喃基或四氢呋喃基;R'是C1-C8卤代烷基,C1-C8烷氧基烷基,C1-C8烷硫基烷基,C1-C8羟烷基,C1-C8酰氧基烷基,C1-C8芳酰氧基烷基,C1-C8氨基烷基,C1-C8烷基氨基烷基,C1-C8二烷基氨基烷基,C1-C8三烷基甲硅烷基烷基,其中每个上述烷基部分可以是直链或支链的; C1-C6烷基苯基,C7-C12芳基烷基,C7-C12烷芳基烷基或杂环烷基,其中杂环部分是吗啉基,哌啶基,吡咯烷基,哌嗪基,环氧乙烷基,氧杂环丁烷基,呋喃基,四氢吡喃基或四氢呋喃基;R5是氢,卤素,甲基,单,二或三卤甲基和R6是定义的脂族或环状侧链在这里。这些化合物可用于抑制生长或复制诸如HIV的逆转录病毒。

著录项

  • 公开/公告号CA2163175C

    专利类型

  • 公开/公告日2007-09-11

    原文格式PDF

  • 申请/专利权人 UNIROYAL CHEMICAL LTD./ UNIROYAL CHEMICAL LTEE.;

    申请/专利号CA19952163175

  • 发明设计人 BROUWER WALTER GERHARD;

    申请日1995-11-17

  • 分类号C07D307/68;A61K31/27;A61K31/33;A61P31/12;C07C251/38;C07C333/08;C07D207/34;C07D263/34;C07D277/56;C07D307/30;C07D309/32;C07D319/12;C07D327/06;C07D333/38;

  • 国家 CA

  • 入库时间 2022-08-21 20:54:21

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