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2--135- 2-Methoxy-135-triazine derivatives its preparation and antiviral pharmaceutical composition comprising the same

机译:2--135- 2-甲氧基-135-三嗪衍生物及其制备方法和包含该衍生物的抗病毒药物组合物

摘要

PURPOSE: 2-Methoxy-1,3,5-triazine derivatives, a preparation method thereof and an antiviral pharmaceutical composition comprising the same are provided. The 2-Methoxy-1,3,5-triazine derivatives inhibit the growth of hepatitis C virus(HCV) and have low toxicity, so that they can be useful for the treatment of hepatitis caused by hepatitis C virus. CONSTITUTION: 2-methoxy-1,3,5-triazine derivatives represented by the formula(1) and pharmaceutically acceptable salts thereof are provided, wherein R is heterocycliccarbonyl or substituted phenyl. A method for preparing the 2-methoxy-1,3,5-triazine derivatives of the formula(1) comprises the steps of: (a) reacting 2-methoxy-6-£4-(4-morpholino) anilino|-4-chloro-1,3,5-triazine of the formula(2) with piperazine of the formula(3) to prepare 2-methoxy-6-£4-(4-morpholino) anilino|-4-(piperazin-1-yl) of the formula(4); and reacting the compound of the formula(4) with heterocycliccarbonyl chloride. A pharmaceutical composition for the prevention and treatment of hepatitis C comprises the 2-methoxy-1,3,5-triazine derivatives of the formula(1) and pharmaceutically acceptable salts thereof as effective components.
机译:用途:提供2-甲氧基-1,3,5-三嗪衍生物,其制备方法和包含其的抗病毒药物组合物。 2-甲氧基-1,3,5-三嗪衍生物抑制丙型肝炎病毒(HCV)的生长且毒性低,因此可用于治疗由丙型肝炎病毒引起的肝炎。组成:提供了由式(1)表示的2-甲氧基-1,3,5-三嗪衍生物及其药学上可接受的盐,其中R为杂环羰基或取代的苯基。制备式(1)的2-甲氧基-1,3,5-三嗪衍生物的方法包括以下步骤:(a)使2-甲氧基-6-£4-(4-吗啉代)苯胺| -4反应式(2)的-氯-1,3,5-三嗪与式(3)的哌嗪制备2-甲氧基-6-£4-(4-吗啉代)苯胺| -4-(哌嗪-1-式(4)的yl);使式(4)的化合物与杂环羰基氯反应。预防和治疗丙型肝炎的药物组合物包含式(1)的2-甲氧基-1,3,5-三嗪衍生物及其药学上可接受的盐作为有效成分。

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