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2-(2,3-dihydro-2-oxo-3-benzofuranyl)acetic acid compounds having antihypoxic and nootropic effects

机译:具有抗氧和促智作用的2-(2,3-二氢-2-氧代-3-苯并呋喃基)乙酸化合物

摘要

The invention relates to new 2-(2,3-dihydro-2-oxo-3- benzofuranyl) acetic acid compounds of general formula I: ##STR1## in which: R.sub.1 denotes a hydrogen atom, a linear or branched alkyl radical having 1 to 4 carbon atoms or a phenyl radical optionally substituted with a halogen atom or with an alkoxy radical containing 1 to 4 carbon atoms or an alkyl radical having 1 to 4 carbon atoms,P PR.sub.2 denotes a hydrogen or halogen atom, a hydroxyl radical, an alkyl radical having 1 to 4 carbon atoms or an alkoxy radical containing 1 to 4 carbon atoms, PPR denotes a hydroxyl radical, a linear or branched alkoxy radical having 1 to 4 carbon atoms, a benzyloxy radical or a radical of general formula A: ##STR2## in which: X and Y, which may be identical or different, each denote a linear or branched alkyl radical containing 1 to 5 carbon atoms, a radical of general formula A.sub.1 (CHZ--COOH)--, in which Z denotes a hydrogen atom, a linear or branched alkyl radical having 1 to 4 carbon atoms, a hydroxyalkyl radical having 1 to 4 carbon atoms, a 4-imidazolylmethylene radical or a benzyl radical optionally substituted with an alkyl radical having 1 to 4 carbon atoms or with a hydroxyl radical; a radical of general formula A.sub.2 (CH.sub.2 W)- in which W denotes a linear or branches dialkylaminomethylene radical having 3 to 9 carbon atoms, a 2- pyrrolidinyl radical optionally substituted with an alkyl radical having 1 to 4 carbon atoms, a benzyl radical, a 1- isochromanyl radical or a 1- isoquinolyl radical, or form, together with the nitrogen to which they are attached, a 2-carboxy-2-pyrrolidinyl radical, a 4-morpholinyl radical, a piperidino radical optionally substituted with a phenyl radical or with an alkoxyphenyl radical having 7 to 10 carbon atoms, or a 1- piperazinyl radical. Medicinal products.
机译:本发明涉及通式I的新的2-(2,3-二氢-2-氧代-3-苯并呋喃基)乙酸化合物:其中R.1代表氢原子,线性或具有1-4个碳原子的支链烷基或任选地被卤素原子或被具有1-4个碳原子的烷氧基取代的苯基或具有1-4个碳原子的烷基,

R。 sub.2表示氢或卤素原子,羟基,具有1至4个碳原子的烷基或含1至4个碳原子的烷氧基,

R表示羟基,直链或支链具有1-4个碳原子的烷氧基,苄氧基或通式A的基团:其中X和Y可以相同或不同,分别表示直链或支链的烷基,其含有1至5个碳原子,通式A.sub.1(CHZ-COOH)-的基团,其中Z表示氢原子,碳原子数为1-4的直链或支链烷基在原子上,具有1-4个碳原子的羟烷基,4-咪唑基亚甲基或苄基,其任选地被具有1-4个碳原子的烷基或羟基取代。通式A.sub.2(CH.sub.2 W)-的基团,其中W表示具有3至9个碳原子的直链或支链二烷基氨基亚甲基基团,2-吡咯烷基可任选地被具有1至2个碳原子的烷基取代4个碳原子,苄基,1-异苯并二氢基或1-异喹啉基或与它们连接的氮一起形成2-羧基-2-吡咯烷基基团,4-吗啉基基团,任选被苯基或具有7至10个碳原子的烷氧基苯基基团取代的哌啶子基基团或1-哌嗪基基团。药品。

著录项

  • 公开/公告号US4859700A

    专利类型

  • 公开/公告日1989-08-22

    原文格式PDF

  • 申请/专利权人 ADIR ET CIE;

    申请/专利号US19880155352

  • 发明设计人 GILBERT LAVIELLE;JEAN LEPAGNOL;

    申请日1988-02-12

  • 分类号A61K31/34;

  • 国家 US

  • 入库时间 2022-08-22 06:27:35

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