首页> 外国专利> DIHYDROPYRIDINE DERIVATIVES, MIXTURE OF THEIR ISOMERS, INDIVIDUAL ISOMERS OR THEIR PHYSIOLOGICALLY TOLERANTABLE SALTS, METHODS OF THEIR SYNTHESIS, INTERMEDIATE COMPOUNDS AND METHOD OF THEIR SYNTHESIS

DIHYDROPYRIDINE DERIVATIVES, MIXTURE OF THEIR ISOMERS, INDIVIDUAL ISOMERS OR THEIR PHYSIOLOGICALLY TOLERANTABLE SALTS, METHODS OF THEIR SYNTHESIS, INTERMEDIATE COMPOUNDS AND METHOD OF THEIR SYNTHESIS

机译:二氢吡啶衍生物,它们的异构体,个体异构体或它们在生理上可降解的盐的混合物,它们的合成方法,中间化合物和它们的合成方法

摘要

FIELD: organic chemistry. SUBSTANCE: derivatives of dihydropyridine of the general formula (I) where: R1 - free aryl with 6-10 carbon atoms or one-three-fold substituted with similar or different substituents taken from the group involving halogen atom, nitro-group, cyano-group, trifluoromethyl, trifluoromethoxy-group and trifluoromethylthio-group; or substituted with direct or branched alkyl with 1-8 carbon atoms that is free or substituted with aryl with 6-10 carbon atoms, or substituted with direct or branched alkoxy-group or alkoxycarbonyl with 1-8 carbon atoms, carboxy-group, amino-group, or the group of the formula -NR4R5, where: R4 and R5 are similar or different and mean hydrogen atom, direct or branched alkyl with 1-8 carbon atoms, phenyl or benzyl; or thienyl; R2- - hydrogen atom or cycloalkyl with 5-8 carbon atoms of direct or branched alkyl, alkenyl, alkadienyl or alkynyl with 1-10 carbon atoms, direct or one-two-substituted similar or different substituents from the group involving halogen atom, hydroxy-group, carboxy-group, cyano-group and nitro-group, or direct or branched alkylthio-group, alkoxy-group, alkoxycarbonyl, acyl or acylhydroxy-group with 1-8 carbon atoms, or cycloalkyl with 3-8 carbon atoms, phenoxy-group or phenyl being the latters are direct or one-two-substituted with similar or different substituents taken from the group involving halogen atom, direct or branched alkyl and alkoxy-group with 1-6 carbon atoms; or substituted with the group -NR4R5, where R4 and R5 have above indicated values; R3- - hydrogen atom or direct or branched alkyl with 1-8 carbon atoms; mixture of their isomers or their individual isomers and their physiologically tolerantable salts. Other objects of invention are method of synthesis of the indicated compounds, medicinal agent containing the indicated substances and method of its preparing. EFFECT: improved method of synthesis. 7 cl, 3 tbl
机译:领域:有机化学。物质:通式(I)的二氢吡啶衍生物。 -含6-10个碳原子或被类似或不同取代基取代的三倍的游离芳基,所述取代基选自卤素原子,硝基,氰基,三氟甲基,三氟甲氧基和三氟甲硫基;或被具有1-8个碳原子的直链或支链烷基取代或被具有6-10个碳原子的芳基取代或由具有1-8个碳原子的直链或支链烷氧基或烷氧羰基,羧基,氨基取代-group或公式-NR 4 R 5 的组,其中:R 4 和R 5 相同或不同,并且是指氢原子,具有1-8个碳原子的直链或支链烷基,苯基或苄基;或噻吩基; R 2 --氢原子或具有5-8个碳原子的直链或支链烷基,烯基,链二烯基或炔基,具有1-10个碳原子,直链或1-2个类似或不同取代基的环烷基选自卤素原子,羟基,羧基,氰基和硝基,或具有1-8个碳原子的直链或支链烷硫基,烷氧基,烷氧基羰基,酰基或酰基羟基,或碳原子数为3-8的环烷基,苯氧基或苯基为后者,直接或被两个或多个相同或不同的取代基取代,所述取代基选自卤素原子,直链或支链烷基和烷氧基,碳原子数为1-6原子或被-NR 4 R 5 组取代,其中R 4 和R 5 具有上述值; R 3 --氢原子或具有1-8个碳原子的直链或支链烷基;它们的异构体或单个异构体与生理上可接受的盐的混合物。本发明的其他目的是合成所示化合物的方法,含有所示物质的药物及其制备方法。效果:改进的合成方法。 7厘升,3汤匙

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