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Meglumine sulfate-catalyzed one-pot green synthesis and antioxidant activity of alpha-aminophosphonates

机译:Meglumine硫酸盐催化的α-氨基膦酸的一锅绿色合成及抗氧化活性

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摘要

A green and efficient synthetic protocol has been developed for the synthesis of a new series of substituted diethyl(((2-methoxy-5-(trifluoromethyl)phenyl)amino)(phenyl)methyl)phosphonates via a one-pot three-component reaction of 2-methoxy-5-trifluoromethyl aniline with various aromatic-substituted aldehydes and diethyl phosphite using meglumine sulfate as an eco-friendly catalyst at room temperature under solvent-free conditions. The merits of this method are high product yield, short reaction time, easy workup, and purification. All the synthesized compounds were evaluated for the antioxidant activity by DPPH, NO, and H2O2 methods using ascorbic acid as a standard. The compounds 4a and 4g showed the highest antioxidant activity than that of the standard ascorbic acid.
机译:已经开发了一种绿色和有效的合成方案,用于合成新的一系列取代的二乙基(((2-甲氧基-5-(三氟甲基)苯基)氨基)(苯基)甲基)膦酸盐,通过单罐三组分反应 在无溶剂条件下,在溶剂条件下在室温下使用Meglumine硫酸盐和硫酸二甲基-5-三氟甲基苯胺,其中硫酸盐作为环型催化剂,在溶剂条件下在室温下作为环型催化剂。 该方法的优点是产品产量,反应时间短,易于余处和纯化。 使用抗坏血酸作为标准,评价所有合成化合物的DPPH,NO和H 2 O 2方法进行抗氧化活性。 化合物4a和4g显示出比标准抗坏血酸的抗氧化活性最高。

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