通过一些芳香族苯羟胺衍生物与乙醛酸的缩合反应合成一些亚胺衍生物及其生物活性研究

Jihad Haji Mohammed, A. Qaddo, Nabaz Salih, Faeza Burhan Omar
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引用次数: 0

摘要

本研究探讨了 N-(3,4-二甲氧基苄基)羟胺和 N-(4-甲基苄基)羟胺与乙醛酸的缩合反应。目的是获得亚胺衍生物作为所需的目标产物。傅立叶变换红外光谱、1H-NMR 和 13C-NMR 光谱技术用于确定生成化合物的结构。这些反应考虑了不同的条件,只有 N-(3,4-二甲氧基苄基)羟胺可以转化为所需的腈酮。最后,评估了其对革兰氏阴性菌大肠杆菌、革兰氏阳性菌金黄色葡萄球菌和真菌白色念珠菌的抗菌效果。活性数据证明,与标准药物相比,这种腈酮具有显著的抗菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Synthesis of Some Imine Derivatives via Condensation Reactions between Some Aromatic Phenylhydroxylamine Derivatives with Glyoxylic Acid and the Study of their biological activity
This study investigated the condensation reactions between N-(3,4-dimethoxybenzyl)hydroxylamine and N-(4-methylbenzyl)hydroxylamine with glyoxalic acid. The objective was to obtain imine derivatives as the desired target products. FT-IR, 1H-NMR, and    13C-NMR spectroscopic techniques were used to identify the structures of the produced compounds. Different conditions were considered for these reactions and only N-(3,4-dimethoxybenzyl)hydroxylamine could be converted to the desired nitrone. Finally, the antimicrobial efficacy was assessed in terms of its action against the bacteria Escherichia coli (E.coli) as Gram-negative bacteria, Staphylococcus aureus (S.aureus) as Gram-positive bacteria and fungus (Candida albicans). The activity data proved that this nitrone showed significant antimicrobial activity compared to standard drugs.
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