首页> 外国专利> NOVEL 3-CHLORO-5-SUBSTITUTED-QUINOXALINE-2-AMINE DERIVATIVES AND PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, METHOD FOR PREPARATION, THERAPEUTIC AGENT FOR ANTIINFLAMMATORY DISEASE INDUCED BY SPC ACTIVITY CONTAINING 3-CHLORO-5-SUBSTITUTED-QUINOXALINE-2-AMINE DERIVATIVES AS AN EFFECTIVE INGREDIENT

NOVEL 3-CHLORO-5-SUBSTITUTED-QUINOXALINE-2-AMINE DERIVATIVES AND PHARMACEUTICALLY ACCEPTABLE SALT THEREOF, METHOD FOR PREPARATION, THERAPEUTIC AGENT FOR ANTIINFLAMMATORY DISEASE INDUCED BY SPC ACTIVITY CONTAINING 3-CHLORO-5-SUBSTITUTED-QUINOXALINE-2-AMINE DERIVATIVES AS AN EFFECTIVE INGREDIENT

机译:新型3-氯5-取代的喹诺啉2-胺衍生物及其药学可接受的盐,其制备方法,包含3-氯5-取代的喹诺酮类药物的SPC活性引起的抗炎性疾病的治疗剂。有效成分

摘要

Provided is a 3-chloro-5-substituted-quinoxaline-2-amine derivative and a therapeutic agent using the 3-chloro-5-substituted-quinoxaline-2-amine derivative so as to treat diseases associated with inflammation. A 3-chloro-5-substituted-quinoxaline-2-amine derivative is represented by the formula 1. In the formula 1, R1 indicates hydrogen, linear or branched C1-C10 alkyl group, C1-C10 alkoxy group or halogen; R2 shows linear or branched C1-C10 alkyl group, C1-C10 alkoxy group, hydroxyl group, halogen group, amine group or substituted amine group, amide group, carbamate group or urea group. In the formula 1, the substituted group indicates a substituted phenyl group wherein one or four groups selected from the group consisting of a linear or branched C1-C10 alkyl group, halogen, nitro group, C1-C10 alkyl group, C1-C10 alkoxy group and C1-C10 haloalkyl group are substituted.
机译:提供3-氯-5-取代-喹喔啉-2-胺衍生物和使用3-氯-5-取代-喹喔啉-2-胺衍生物的治疗剂,以治疗与炎症有关的疾病。 3-氯-5-取代的喹喔啉-2-胺衍生物由式1表示。式1中,R 1表示氢,直链或支链的C 1 -C 10烷基,C 1 -C 10烷氧基或卤素。 R 2表示直链或支链的C 1 -C 10烷基,C 1 -C 10烷氧基,羟基,卤素基,胺基或取代的胺基,酰胺基,氨基甲酸酯基或脲基。在式1中,取代基表示取代苯基,其中选自直链或支链C1-C10烷基,卤素,硝基,C1-C10烷基,C1-C10烷氧基的一个或四个基团。 C1-C10卤代烷基被取代。

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