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Synthesis and Biological Evaluation of Mannich Bases of Isoxazoline Derivatives as Novel Anti-Microbial Agents

机译:异恶唑啉衍生物作为新型抗微生物剂的曼尼希碱的合成与生物学评价

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摘要

A novel series of compounds were synthesized by condensation reaction of substituted acetophenone (1a-b) with substituted aldehyde (2a-b) in presence of alcoholic sodium hydroxide to get intermediate chalcones (3a-c), which were further treated with hydroxylamine hydrochloride in presence of sodium hydroxide to get isoxazolines derivatives (4a-c). The latter were refluxed with substituted primary amines and formaldehyde for 6-10 h to afford Mannich bases. The synthesized compounds were characterized on the basis of their spectral (IR, 1HNMR) data and evaluated for the antimicrobial activity by using Zone of Inhibition by cup plate method and Minimum Inhibitory Concentration by broth dilution method.
机译:通过在含醇氢氧化物存在下与取代的醛(2a-b)的取代醛(2a-b)的缩合反应合成了一种新的化合物,得到中间丘酮(3a-c),其用盐酸羟胺进一步处理氢氧化钠的存在得到异恶唑啉衍生物(4A-C)。后者用取代的伯胺和甲醛回流6-10小时,以提供Mannich碱。合成化合物的特征在于它们的光谱(IR,1HNMR)数据,并通过使用杯板方法和通过肉汤稀释方法使用抑制区和最小抑制浓度来评估抗微生物活性。

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