(±)-R,S-2-Chloro-N-(4-methyl-2-oxo-2H-chromen-7-yl)-2-phenylacetamide

Molbank Pub Date : 2024-06-03 DOI:10.3390/m1830
D. Dimitrova, S. Manolov, D. Bojilov, I. Ivanov, P. Nedialkov
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Abstract

In this study, we report the synthesis of (±)-2-chloro-N-(4-methyl-2-oxo-2H-chromen-7-yl)-2-phenylacetamide through the reaction of 7-amino-4-methyl-2H-chromen-2-one with (±)-2-chloro-2-phenylacetyl chloride. The in vitro anti-inflammatory activity of the new compound was evaluated, and the results indicated that it exhibited superior activity compared to the standard, ibuprofen. The bio-functional hybrid compound underwent thorough detailed characterization utilizing 1H and 13C NMR, UV, and mass spectral analysis.
(±)-R,S-2-Chloro-N-(4-methyl-2-oxo-2H-chromen-7-yl)-2-phenylacetamide
在这项研究中,我们报告了通过 7-氨基-4-甲基-2H-苯并吡喃-2-酮与 (±)-2-chloro-2-phenylacetyl chloride 反应合成 (±)-2-chloro-N-(4-methyl-2-oxo-2H-chromen-7-yl)-2-phenylacetamide 的过程。对新化合物的体外抗炎活性进行了评估,结果表明,与标准药物布洛芬相比,新化合物具有更高的活性。利用 1H 和 13C NMR、紫外线和质谱分析,对生物功能杂化化合物进行了全面细致的表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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