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首页> 外文期刊>Chemistry of heterocyclic compounds >Facile Regioselective On-Water Synthesis of 4,7-Dihydropyrazolo[1,5-a]Pyrimidines and 4,7-Dihydro[1,2,4]Triazolo[1,5-a]Pyrimidines
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Facile Regioselective On-Water Synthesis of 4,7-Dihydropyrazolo[1,5-a]Pyrimidines and 4,7-Dihydro[1,2,4]Triazolo[1,5-a]Pyrimidines

机译:体内完全合成4,7-二氢吡唑[1,5-A]嘧啶和4,7-二氢[1,2,4]三唑唑[1,5-A]嘧啶

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摘要

Efficient and regioselective on-water synthesis of variously substituted 5-amino-4,7-dihydropyrazolo[1,5-a]pyrimidine-6-carbonitriles and 5-amino-4,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidine-6-carbonitriles using 1,8-diazabicyclo[5.4.0]undec-7-ene as catalyst has been demonstrated. The reaction of 2-benzylidenemalononitriles and 3-aryl-1H-pyrazol-5-amines or 1H-1,2,4-triazol-5-amine allows to obtain the respective pyrazolo[1,5-a]pyrimidines and [1,2,4]triazolo[1,5-a]pyrimidines in high yields up to 93%. Main advantages of the developed synthetic protocol are application of water as environmentally friendly solvent, short reaction times, simple workup procedure that often does not require further purification of products, and broad substrate scope.
机译:水性有效和区域各种替代的5-氨基-4,7-二氢吡唑[1,5-A]嘧啶-6-腈和5-氨基-4,7-二氢[1,2,4]三唑唑[ 如图1,5-A]嘧啶-6-碳腈,使用1,8-二氮杂双环[5.4.0] UNDEC-7-ENE作为催化剂。 2-苄基甲醛和3-芳基-1H-吡唑-5-胺或1H-1,2,4-三唑-5-胺的反应允许获得各自的吡唑[1,5-A]嘧啶和[1, 2,4]三唑[1,5-A]嘧啶高产率高达93%。 发达的合成方案的主要优点是将水作为环保溶剂,反应时间短,往往不需要进一步纯化产物的简单余介质和宽基板范围。

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