首页> 外文期刊>Journal of Advanced Physics >Synthesis, Characterization and Biological Activity Studies on 6-Alkyl-5,6-Dihydrobenzoimidazo [1,2-c]Quinazoline Derivatives
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Synthesis, Characterization and Biological Activity Studies on 6-Alkyl-5,6-Dihydrobenzoimidazo [1,2-c]Quinazoline Derivatives

机译:6-烷基-5,6-二氢苯并咪唑并[1,2-c]喹唑啉衍生物的合成,表征和生物活性研究

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摘要

Reaction of aminophenyl benzimidazole with propionaldehyde, i-butyraldehyde and i-valeraldehyde in alcohol resulted in the ethyl, isopropyl and isobutyl derivatives (I, II and III) of dihydrobenzoimidazo[1,2-c] quinazoline, respectively. All the products were characterized by elemental analysis, IR, UV-Vis, ~1H NMR, ~(13)C NMR and X-ray crystal structure analysis. The antimicrobial activities of these compounds against four bacterial strains (Bacillus subtilis, Staphylococcus aureus, Escherichia coli and Pseudomonas) and two fungal strains (Cryptococcus neoformans and Candida albicans) were evaluated. Compounds I and III crystallized in the orthorhombic Pna2_1 space group whereas the compound II crystallized in the monoclinic P2_1/c space group. The structures I, II and III were solved and refined to R-values of 0.0336, 0.0353 and 0.0387 respectively. A comparative study of the crystal structures of these compounds is also given in this paper.
机译:氨基苯基苯并咪唑与丙醛,异丁醛和异戊醛在醇中的反应分别产生了二氢苯并咪唑并[1,2-c]喹唑啉的乙基,异丙基和异丁基衍生物(I,II和III)。所有产品均通过元素分析,IR,UV-Vis,〜1H NMR,〜(13)C NMR和X射线晶体结构分析进行了表征。评价了这些化合物对四种细菌菌株(枯草芽孢杆菌,金黄色葡萄球菌,大肠埃希菌和假单胞菌)和两种真菌菌株(新隐球菌和白色念珠菌)的抗菌活性。化合物I和III在正交晶体Pna2_1空间群中结晶,而化合物II在单斜晶P2_1 / c空间群中结晶。解析结构I,II和III并将其精炼为R值0.0336、0.0353和0.0387。本文还对这些化合物的晶体结构进行了比较研究。

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