首页> 外文期刊>Rasayan Journal of Chemistry >SYNTHESIS OF SOME1,4,5-TRISUBSTITUTED 1,2,3-TRIAZOLES BY 1,3-DIPOLAR CYCLOADDITION OF 2-SUBSTITUTED PHENYL AZIDES TO DIMETHYL ACETYLENE DICARBOXYLATE (DMAD), REGULAR STIRRING VERSUS MICROWAVE IRRADIATION:A COMPARATIVE STUDY
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SYNTHESIS OF SOME1,4,5-TRISUBSTITUTED 1,2,3-TRIAZOLES BY 1,3-DIPOLAR CYCLOADDITION OF 2-SUBSTITUTED PHENYL AZIDES TO DIMETHYL ACETYLENE DICARBOXYLATE (DMAD), REGULAR STIRRING VERSUS MICROWAVE IRRADIATION:A COMPARATIVE STUDY

机译:2-取代的叠氮化叠氮与二乙炔二甲酸二甲酯(DMAD)的1,3-二氯环化反应合成1,4,5-三取代的1,2,3-三唑类化合物,对微波辐射进行了常规搅拌与对比研究

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摘要

1,4,5-trisubstituted 1,2,3-triazoles were prepared by 1,3-dipolar cycloaddition reaction of some 2-substituted phenyl azides to dimethylacetylene dicarboxylate (DMAD) under regular stirring at room temperature or under microwave irradiation. The targeted compounds were obtained in good to excellent yields. The use of microwave irradiation gives the highest yields in few minutes and proper products.
机译:在室温下或在微波辐射下,通过一些2-取代的苯基叠氮化物与1,2-甲基二乙炔二羧酸二甲酯(DMAD)的1,3-偶极环加成反应,制得1,4,5-三取代的1,2,3-三唑。以良好至优异的产率获得了目标化合物。使用微波辐照可在数分钟内获得最高产量,并提供合适的产品。

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