An Efficient Synthesis of Thiazolo and Thiadiazolo Quinoxaline Derivatives in Ionic Liquid

B. Prasanna, B. Srinivas, Y. Jagannadham, Sumangala Rao
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引用次数: 2

Abstract

A series of 3-substitutedphenyl-1-thia-tetrazopentaleno[1,2-b] naphthalene 4(a-d) and 2-substitutedphenyl-1-thia-pentazopentaleno[1,2-b] naphthalene 5(a-d) were synthesized via., the reaction of 2-aminothiazoles 2(a-d) and 2-aminothiadiazoles 3(a-d) with 2,3-dichloro quinoxaline 1 in ionic liquid without using any catalyst. This protocol has the advantages of easier workup, milder reaction conditions, high yields, and environmentally benign procedure over traditional methods. The synthesized compounds 4(a-d) and 5(a-d) tested for their anti-fungal activity and these compounds were characterized by IR, NMR and Mass spectral analysis.
离子液体中噻唑啉和噻二唑啉喹诺啉衍生物的高效合成
合成了一系列3-取代苯基-1-硫-四氮戊二烯[1,2-b]萘4(A -d)和2-取代苯基-1-硫-五氮戊二烯[1,2-b]萘5(A -d)。2-氨基噻唑2(a-d)和2-氨基噻二唑3(a-d)与2,3-二氯喹啉1在离子液体中不使用任何催化剂的反应。与传统方法相比,该方法具有操作简单、反应条件温和、产率高、环境友好等优点。对合成的化合物4(a-d)和5(a-d)进行了抗真菌活性测试,并通过IR、NMR和质谱对其进行了表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
E-journal of Chemistry
E-journal of Chemistry CHEMISTRY, MULTIDISCIPLINARY-
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