Synthesis and Characterization of New benzimidazole-nitrone Derivatives, and Study of Their Effect as Anti-bacterial.

None Meaad A. Fadel, None Hanaa K. Mousa, None Dawood S. Ali
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Abstract

New benzimidazole derivatives (benzimidazole-nitrone) were synthesized from the condensation of o-phenylene diamine with p-amino benzaldehyde in the presence of (P-TsOH\EtOH). Then the benzimidazole compounds that containing an imine group were oxidized to obtain a nitrone group by used peracetic acid and identified by FT-IR, H1-NMR spectra, and elemental analysis. All compounds applied to the Escherichia coli and Staphylococcus aureus gave a different result. The compounds which have (OH, Br, Cl, OCH3) groups appeared activity as anti-bacterial while compound (2) when R=H don’t have activity for each type of bacteria that used
新型苯并咪唑-硝基衍生物的合成、表征及抗菌作用研究。
在(P-TsOH\EtOH)存在下,邻苯二胺与对氨基苯甲醛缩合合成了新的苯并咪唑衍生物(苯并咪唑-硝基酮)。然后用过氧乙酸将含亚胺基的苯并咪唑类化合物氧化为硝酮基,并通过FT-IR、H1-NMR和元素分析对其进行鉴定。所有应用于大肠杆菌和金黄色葡萄球菌的化合物都给出了不同的结果。含有(OH, Br, Cl, OCH3)基团的化合物表现出抗菌活性,而当R=H时,化合物(2)对所使用的每种细菌都没有活性
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