Synthesis and biological evaluations of sulfa derivatives bearing heterocyclic moieties.

Bollettino chimico farmaceutico Pub Date : 2004-07-01
Wafaa R Abdel-Monem
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Abstract

Some new sulfa derivatives bearing a heterocyclic moieties fural, pyrimidinone, thiazolidinone, benzimidazole and 1,2,4-triazinone and the related compounds 2-19 have been synthesized from treatment of sulfa drugs with thioisocyanate, acid chlorides, 3-chloro-1,2,4-triazines, aldehydes, esters and/or 2-methylbenzoxazole followed by ring closure reactions. Structures of the products have been deduced from their elemental analysis and spectral data. Significant antimicrobial activities were observed in vitro for some members of the series. Compounds 9b, 16 are highly active, while compounds 4b, 6d, 7,9a, 10 and 14 showing a moderate active towards gramme positive bacterium (b.subtilis). gramme negative bacterium (E. coli) and two fungi namely (A.nidulans & A.terreus).

含杂环磺胺衍生物的合成及生物学评价。
以硫代异氰酸酯、酸性氯化物、3-氯-1,2,4-三嗪、醛类、酯类和/或2-甲基苯并恶唑处理磺胺类药物,然后进行封环反应,合成了一些新的含杂环部分的呋喃醛、嘧啶、噻唑烷酮、苯并咪唑和1,2,4-三嗪酮及其相关化合物2-19。通过元素分析和光谱数据推导出产物的结构。该系列的一些成员在体外观察到显著的抗菌活性。化合物9b、16对革兰氏阳性菌(枯草芽孢杆菌)具有高活性,而化合物4b、6d、7、9a、10和14对革兰氏阳性菌(枯草芽孢杆菌)具有中等活性。革兰氏阴性细菌(大肠杆菌)和两种真菌,即(A.nidulans和A.terreus)。
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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