4-(5-苯基-1,3,4-恶二唑-2-基)苯胺衍生新化合物的合成及其生物活性研究

IF 0.8 4区 化学 Q4 CHEMISTRY, ORGANIC
K. A. Alheety, N. M. Jamel, W. M. Abd-Al Hameed, M. S. Al-Rawi, J. H. Tomma
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引用次数: 0

摘要

通过序列反应制备了一系列新的含有 1,3,4-恶二唑环的 N-酰基衍生物(4a-4d)和氮杂环丁烷-2-酮衍生物(5a, 5b)。作为起始材料的新希夫碱(3a-3d)是通过(4-(5-苯基-1,3,4-恶二唑-2-基)苯胺)与四个被取代的芳香族二醛(2a-2d)缩合制备的。新合成的希夫碱(3a-3d)与乙酰氯在干苯中反应,得到新的衍生物(4a-4d)。第二条途径是希夫碱与氯乙酰氯在二噁烷和三乙胺中于 0-5°C 发生环化反应,生成新的氮杂环丁烷-2-酮衍生物(5a、5b)。合成的化合物通过傅立叶变换红外光谱和 1H NMR 光谱进行表征,以阐明其结构。最后,对所合成的产品进行了药效测定,结果表明其对两种细菌具有极佳至良好的抗菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthesis and Study of the Biological Activity of New Compounds Derived from 4-(5-Phenyl-1,3,4-oxadiazole-2-yl)aniline

Synthesis and Study of the Biological Activity of New Compounds Derived from 4-(5-Phenyl-1,3,4-oxadiazole-2-yl)aniline

A new series of N-acyl derivatives (4a–4d) and Azetidin-2-one derivatives (5a, 5b) containing a 1,3,4-oxadiazole ring were prepared by sequence reactions. The new Schiff bases (3a–3d) used as starting materials were prepared via condensation of (4-(5-phenyl-1,3,4-oxadiazole-2yl)aniline) with four replaced aromatic dialdehyde (2a–2d). The newly synthesized Schiff bases (3a–3d) reacted with, acetyl chloride in the dry benzene to get new derivatives (4a–4d). While the second path was towards the formation of new Azetidin-2-one derivatives (5a, 5b) from cyclization reaction of the Schiff bases with chloroacetylchloride in dioxan and triethylamine at 0–5°C. Synthesized compounds had been characterized by FT-IR and 1H NMR spectra in order to elucidate their structures. Finally, the resulting products were evaluated for it is efficacy measurements against two types of bacteria showed excellent to good efficacy antibacterial activity.

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来源期刊
CiteScore
1.40
自引率
25.00%
发文量
139
审稿时长
3-6 weeks
期刊介绍: Russian Journal of Organic Chemistry is an international peer reviewed journal that covers all aspects of modern organic chemistry including organic synthesis, theoretical organic chemistry, structure and mechanism, and the application of organometallic compounds in organic synthesis.
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