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Synthesis of 1-(5-Chloro-2-hydroxyphenyl)-5-oxopyrrolidine-3-carboxylic Acid Derivatives and Their Antioxidant Activity

机译:1-(5-氯-2-羟基苯基)-5-氧吡咯烷-3-羧酸衍生物的合成及其抗氧化活性

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摘要

A series of novel 1-(5-chloro-2-hydroxyphenyl)-5-oxopyrrolidine-3-carboxylic acid derivatives containing chloro, hydroxyl, isopropyl, nitro, nitroso, and amino substituents at benzene ring and 1-(5-chloro-2-hydroxyphenyl)-5-oxopyrrolidine-3-carbohydrazide derivatives bearing heterocyclic moieties were synthesized. Antioxidant activity of the synthesized compounds was screened by DPPH radical scavenging method and reducing power assay. A number of compounds were identified as potent antioxidants. Antioxidant activity of 1-(5-chloro-2-hydroxyphenyl)-4-(5-thioxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)pyrrolidin-2-one has been tested to be 1.5 times higher than that of a well-known antioxidant ascorbic acid. 1-(5-Chloro-2-hydroxyphenyl)-4-(4-methyl-5-thioxo-4,5-dihydro-1H-1,2,4-triazol-3-yl)pyrrolidin-2-one has shown 1.35 times higher antioxidant activity than that of vitamin C by DPPH radical scavenging method and optical density value of 1.149 in reducing power assay. The structure of 1-(5-chloro-2-hydroxyphenyl)-N-(1,3-dioxoisoindolin-2-yl)-5-oxopyrrolidine-3-carboxamide was unambiguously assigned by means of X-ray diffraction analysis data.
机译:一系列新颖的1-(5-氯-2-羟苯基)-5-氧吡咯烷-3-羧酸衍生物,在苯环和1-(5-氯代-苯基)上含有氯,羟基,异丙基,硝基,亚硝基和氨基取代基合成了带有杂环部分的2-羟基苯基)-5-氧吡咯烷-3-碳酰肼衍生物。通过DPPH自由基清除法和还原能力测定法筛选合成的化合物的抗氧化活性。许多化合物被确定为有效的抗氧化剂。已测试1-(5-氯-2-羟基苯基)-4-(5-硫代氧杂4,5-二氢-1,3,4-恶二唑-2-基)吡咯烷酮-2-酮的抗氧化活性为比众所周知的抗氧化剂抗坏血酸高1.5倍。 1-(5-氯-2-羟基苯基)-4-(4-甲基-5-硫代-4-5,5-二氢-1H-1,2,4-三唑-3-基)吡咯烷酮-2-一DPPH自由基清除法的抗氧化活性是维生素C的1.35倍,在降低功率测定中的光密度值为1.149。通过X射线衍射分析数据明确分配了1-(5-氯-2-羟基苯基)-N-(1,3-二氧代异吲哚-2-基)-5-氧吡咯烷-3-羧酰胺的结构。

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