首页> 外文期刊>Pharmaceutical Chemistry Journal >A SIMPLE MEANS OF PREPARING QUINOXALINE DERIVATIVES: DIRECT INTRODUCTION OF C-NUCLEOPHILES INTO THE QUINOXALINE NUCLEUS BY SUBSTITUTING A HYDROGEN ATOM
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A SIMPLE MEANS OF PREPARING QUINOXALINE DERIVATIVES: DIRECT INTRODUCTION OF C-NUCLEOPHILES INTO THE QUINOXALINE NUCLEUS BY SUBSTITUTING A HYDROGEN ATOM

机译:制备喹喔啉衍生物的简单方法:通过取代氢原子将C-核素直接引入喹喔啉核中

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摘要

Unsubstituted quinoxaline (I) reacts with dimedone, indanedione, and l-phenyl-3-methylpyrazol-5-one in dimethylsulfoxide in the presence of acid to form monosubstitution products II - IV. Quinoxaline reacts with 1,3-dimethylbarbituric acid in dimethylsulfoxide solution at room temperature to form monosubstitution product V without external catalysis. Heating of I with resorcinol in ethanol in the presence of acid produced resorcinol derivative VI. In the presence of base, quinoxaline reacts with l-phenyl-3-methylpyrazol-5-one to form dipyrazolylmethane VII and tetrapyrazolylethane derivative VIII. Compound VIII undergoes cleavage to form dipyrazolylmethane VII in dimethylformamide solution with boiling or in the presence of iodine at room temperature.
机译:在酸的存在下,未取代的喹喔啉(Ⅰ)在二甲基亚砜中与二甲酮,茚二酮和1-苯基-3-甲基吡唑-5-酮反应形成单取代产物Ⅱ-Ⅳ。喹喔啉在室温下与1,3-二甲基巴比妥酸在二甲基亚砜溶液中反应,形成单取代产物V,而无需外部催化。在酸存在下将I与间苯二酚在乙醇中加热产生间苯二酚衍生物VI。在碱的存在下,喹喔啉与1-苯基-3-甲基吡唑-5-酮反应形成二吡唑基甲烷VII和四吡唑基乙烷衍生物VIII。化合物VIII在沸腾下或在碘的存在下于室温下,在二甲基甲酰胺溶液中裂解形成二吡唑基甲烷VII。

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