首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Synthesis and Biological Activity of Some 3-Aryl-3,4-dihydro-2H-benz[e]-1,3-oxazines/6-bromo-3-aryl-3,4-dihydro-2H-benz[e]-1,3-oxazines
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Synthesis and Biological Activity of Some 3-Aryl-3,4-dihydro-2H-benz[e]-1,3-oxazines/6-bromo-3-aryl-3,4-dihydro-2H-benz[e]-1,3-oxazines

机译:某些3-芳基-3,4-二氢-2H-苯并[e] -1,3-恶嗪/ 6-溴-3-芳基-3,4-二氢-2H-苯并[e]-的合成及生物活性1,3-恶嗪

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摘要

N-(2-Hydroxy)-benzyl-arylamine (1) gives substantially pure 3-aryl-3,4-dihydro-2H-benz[e]-1,3-oxazines/6-bromo-3-aryl-3,4-dihydro-2H-benz[e]-1,3-oxazines (2) on cyclization with formaldehyde in methanol within 0.5-1.0 h at 65-68 °C in excellent yields. The compounds thus prepared were screened for their antimicrobial studies against Gram-positive bacteria (Staphylococcus aureus, MTCC 96) and Gram-negative bacteria (E. coli, MTCC 739). For estimating antifungal activity the organism used is Candida albicans. Minimum inhibitory concentration of all the compounds was determined using the micro-broth dilution method.
机译:N-(2-羟基)-苄基-芳基胺(1)得到基本上纯的3-芳基-3,4-二氢-2H-苯并[e] -1,3-恶嗪/ 6-溴-3-芳基-3, 4-二氢-2H-苯并[e] -1,3-恶嗪(2)在65-68°C下于0.5-1.0 h内与甲醛在甲醇中环化,收率很高。筛选由此制备的化合物用于针对革兰氏阳性细菌(金黄色葡萄球菌,MTCC 96)和革兰氏阴性细菌(大肠杆菌,MTCC 739)的抗微生物研究。为了估计抗真菌活性,使用的生物是白色念珠菌。使用微浓稀释法测定所有化合物的最小抑菌浓度。

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