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首页> 外文期刊>Russian Journal of Organic Chemistry >Microwave-Assisted Synthesis of 2-Aryl(hetaryl)-5-phenylamino-1,3,4-thiadiazoles from 5-Substituted Tetrazoles
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Microwave-Assisted Synthesis of 2-Aryl(hetaryl)-5-phenylamino-1,3,4-thiadiazoles from 5-Substituted Tetrazoles

机译:微波辅助从5-取代的四唑合成2-芳基(杂芳基)-5-苯基氨基-1,3,4-噻二唑

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摘要

In the recent years 2-aryl-5-arylamino-1,3,4-thia-diazoles have attracted considerable attention due to their intrinsic high biological activity [1]. Compounds of the 2-aryl-5-arylamino-1,3,4-thiadiazole series were found to exhibit antimicrobial [2], antituberculous [3], and antiphlogistic properties [4], as well as to inhibit development of some cancer diseases [5]. However, the lack of convenient methods for the preparation of 2,5-disubstituted 1,3,4-thiadiazoles strongly restricts their potential application in medical practice. Known and widely used methods of synthesis of 2,5-disubstituted 1,3,4-thiadiazoles often include a number of steps and are insufficiently effective [1, 6]. On the other hand, as early as 1961 Huisgen et al. [7] reported a simple one-step procedure for the synthesis of 2-phenyl-5-phenylamino-1,3,4-thiadiazole from 5-phenyl-1H-tetrazole and phenyl isothiocyanate.
机译:近年来,由于2-芳基-5-芳基氨基-1,3,4-噻二唑因其固有的高生物活性而引起了相当大的关注[1]。发现2-芳基-5-芳基氨基-1,3,4-噻二唑系列化合物具有抗菌[2],抗结核[3]和消炎特性[4],并抑制某些癌症疾病的发展[5]。但是,缺乏方便的制备2,5-二取代的1,3,4-噻二唑的方法极大地限制了它们在医学实践中的潜在应用。合成2,5-二取代的1,3,4-噻二唑的已知方法和广泛使用的方法通常包括许多步骤,效果不佳[1,6]。另一方面,早在1961年,Huisgen等人。 [7]报道了一种简单的一步步骤,由5-苯基-1H-四唑和异硫氰酸苯酯合成2-苯基-5-苯基氨基-1,3,4-噻二唑。

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