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Microwave-enhanced reactions of 4-amino-5-merecapto-1,2,4-triazoles with benzoyl chloride and aromatic aldehydes

机译:4-氨基-5-巯基-1,2,4-三唑与苯甲酰氯和芳香醛的微波增强反应

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摘要

The microwave-enhanced reactions of 4-amino-5-mercapto-3-substituent-1,2,4-triazoles with benzoyl chloride or arylaldehydes under solvent-free conditions without catalyst were studied. 3-Substituded-6-phenyl-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles were easily prepared by the reactions of 4-amino-5-merecapto-3-substituded-1,2,4-triazoles with benzoyl chloride. 4-Arylideneamino-5-mercapto-3-substituted-1,2,4-triazoles were obtained by the condensation of 4-amino-5-mercapto-3-substituent-1,2,4-triazoles with arylaldehydes. This method possessed such advantages as short reaction time, environmentally benign procedures, easy purification, and high yield.
机译:研究了在无催化剂的条件下,无溶剂条件下4-氨基-5-巯基-3-取代基1,2,4-三唑与苯甲酰氯或芳醛的微波增强反应。通过3-氨基-5-merecapto-3-substituded-1的反应可轻松制备3-subsubdated-6-苯基-1,2,4-三唑[3,4-b] -1,3,4-噻二唑,2,4-三唑与苯甲酰氯。通过4-氨基-5-巯基-3-取代基-1,2,4-三唑与芳基醛的缩合反应获得4-亚芳基氨基-5-巯基-3-取代的1,2,4-三唑。该方法具有反应时间短,对环境无害,易于纯化,收率高等优点。

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