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Synthesis, antimicrobial and anti-HIV activity of some novel benzenesulfonamides bearing 2,5-disubstituted-1,3,4-oxadiazole moiety

机译:一些带有2,5-二取代-1,3,4-恶二唑部分的新型苯磺酰胺的合成,抗菌和抗HIV活性

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摘要

Twelve novel primary (4a-c, 5a-c) and secondary (4d-f, 5d-f) benzenesulfonamides bearing 2,5-disubstituted-1,3,4-oxadiazole moiety have successfully been prepared by direct chlorosulfonation of phenyl substitutent present on the 2-position of 5-mercapto-1,3,4-oxadiazoles 2a-c and their methylhio derivatives 3a-c using chlorosulfonic acid under anhydrous conditions. Structures of the synthesized compounds were established by their physical and spectral data. Some of the synthesized compounds have been screened in vitro for their antimicrobial and anti-HIV activity; the results were in accordance with SAR.
机译:通过直接存在的苯基取代基的氯磺化反应,已经成功制备了十二种新型的带有2,5-二取代-1,3,4-恶二唑部分的伯(4a-c,5a-c)和仲(4d-f,5d-f)苯磺酰胺。在无水条件下,使用氯磺酸在5-巯基-1,3,4-恶二唑2a-c及其甲基巯基衍生物3a-c的2-位上合成。合成化合物的结构通过其物理和光谱数据确定。已经从体外筛选了一些合成的化合物的抗微生物和抗HIV活性。结果与SAR一致。

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