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Synthesis and Antioxidant Activity Studies of Some 5-Chloro-3-substituted 2(3H)-Benzoxazolone Derivatives

机译:一些5-氯-3-取代的2(3H)-苯并恶唑啉酮衍生物的合成和抗氧化活性研究

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摘要

2(3H)-Benzoxazolone derivatives are versatile heterocyclic compounds since they display a wide range of pharmacological properties. On the other hand, anilide pharmacophore has been known in medicinal chemistry as an useful template in various pharmacological states. In this study, we synthesized eleven 5-chloro-2(3H)-benzoxazolone-3-alkananiIide derivatives and evaluated their antioxidant activities. The structural confirmation of the title compounds was achieved by spectral and analytical data. The antioxidant capacity of the synthesized compounds was determined by the 2,2-diphenyl-2-picrylhydrazyl hydrate (DPPH) and 2,2-azinobis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS) radicals scavenging assays. The results indicated that the majority of the compounds were effective in both tests. The most active compound in the series was compound 6, bearing 4-methoxy substituent on the N-phenyl ring of the propionanilide skeleton.
机译:2(3H)-苯并恶唑啉酮衍生物是通用的杂环化合物,因为它们具有广泛的药理特性。另一方面,在医学化学中已知苯胺基药效团作为各种药理学状态的有用模板。在这项研究中,我们合成了11种5-氯-2(3H)-苯并恶唑酮-3-链烷胺衍生物,并评估了其抗氧化活性。通过光谱和分析数据获得标题化合物的结构确认。合成的化合物的抗氧化能力通过2,2-二苯基-2-吡啶基肼基水合物(DPPH)和2,2-叠氮基双(3-乙基苯并噻唑啉-6-磺酸)(ABTS)自由基清除试验来确定。结果表明,大多数化合物在两种测试中均有效。该系列中活性最高的化合物是在丙酰苯胺骨架的N-苯环上带有4-甲氧基取代基的化合物6。

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