首页> 外国专利> 2,3-DIOXO-1,2,3,4- TETRAHYDRO- QUINOXALINYL DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

2,3-DIOXO-1,2,3,4- TETRAHYDRO- QUINOXALINYL DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM

机译:2,3-二氧-1,2,3,4-四氢-喹喔啉基衍生物,其制备方法和包含它们的药物组合物

摘要

Anti-convulsive 2,3-dioxo-1,2,3,4- tetrahydro-quinoxalinyl derivatives of the formula wherein one of the radicals R1 and R2 is hydrogen and the other is a group of formula -alk-N(R8)-X- R7, -alk-O-X-R7 or -alk-S-X-R7, one of the radicals R3 and R4 is hydrogen, halogen or nitro and the other is halogen or nitro, R7 is carboxy, lower alkoxycarbonyl; phenyl-lower alkoxycarbonyl that is unsubstituted or substituted by lower alkyl, lower alkoxy, hydroxy, halogen and/or by trifluoromethyl; carbamoyl; phenylcarbamoyl that is unsubstituted or substituted by lower alkyl, lower alkoxy, hydroxy, halogen, nitro, carboxy, lower alkoxycarbonyl, phenyl, phenyloxy and/or by trifluoromethyl; phosphono, mono- di- or tri-lower alkylphosphono or tetrazolyl, R8 is hydrogen, lower alkyl or, together with X and the nitrogen atom bonding R8 and X forms a pyrrolidinylene, piperidinylene or piperazinylene radical, alk is lower alkylene, and X (unless, המדפיס הממשלתי מכשיר שרת, יומן הפטנטים, עמ' together with R7 and R8 and the nitrogen atom bonding R8 and X, it forms part of one of the mentioned ring systems) is a direct bond, C1-C7 alkylene, C1-C4 alkylidene, oxo-C1-C4 alkylene including carbonyl, oxo-C1-C4 alkenylene, amino-C1-C4 alkylidene, oxo-C1-C4 alkylene including carbonyl, oxo-C1-C4 alkenylene, amino-C1-C4 alkylidene, carboxy-C1-C4 alkylidene, C1-C4-alkoxycarbonyl-C1-C4 alkylidene, g-aza-a oxo-C1-C4alkylene or g-aza-a oxo-C1-C4 alkenylene, or unsubstituted or halo- and/or trifluoromethyl-substituted phenyl-C1-C4 alkylidene, or salts thereof. _______________
机译:下式的抗惊厥2,3-二氧-1,2,3,4-四氢-喹喔啉基衍生物,其中基团R1和R2之一为氢,另一个为基团-alk-N(R8)- X-R7,-alk-OX-R7或-alk-SX-R7,基团R3和R4之一为氢,卤素或硝基,另一个为卤素或硝基,R7为羧基,低级烷氧羰基;未取代或被低级烷基,低级烷氧基,羟基,卤素和/或三氟甲基取代的苯基-低级烷氧羰基;氨基甲酰基;未取代或被低级烷基,低级烷氧基,羟基,卤素,硝基,羧基,低级烷氧羰基,苯基,苯氧基和/或三氟甲基取代或取代的苯基氨基甲酰基;膦酰基,单-或二-低级烷基膦酰基或四唑基,R 8为氢,低级烷基,或与X和氮原子键合的R 8和X形成吡咯烷基,哌啶基或哌嗪基,烷基为低级亚烷基,X(除非,המדפיסהממשלתימכשירשרת,יומןהפטנטים,עמ'与R7和R8以及氮原子键合R8和X,形成上述环系统之一的一部分)是直接键,C1-C7亚烷基,C1-C4亚烷基,含羰基的氧代-C1-C4亚烷基,氧代-C1-C4亚烯基,氨基-C1-C4亚烷基,含羰基的氧代-C1-C4亚烷基,氧代-C1-C4亚烯基,氨基-C1-C4亚烷基,羧基- C 1 -C 4亚烷基,C 1 -C 4烷氧基羰基-C 1 -C 4亚烷基,g-氮杂-氧代-C 1 -C 4亚烷基或g-氮杂-氧代-C 1 -C 4亚烯基,或未被取代或被卤代和/或三氟甲基取代苯基-C 1 -C 4亚烷基或其盐。 _______________

著录项

  • 公开/公告号IL122987B

    专利类型

  • 公开/公告日2001-08-08

    原文格式PDF

  • 申请/专利权人 NOVARTIS AG;

    申请/专利号IL122987

  • 发明设计人

    申请日1996-08-19

  • 分类号C07D241/52;A61K31/495;A61K31/675;A61P25/00;A61P43/00;C07D401/12;C07D401/14;C07D403/12;C07D403/14;C07F9/547;

  • 国家 IL

  • 入库时间 2022-08-22 01:25:06

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