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Synthesis of new pyrazole derivatives via multicomponent reaction and evaluation of their antimicrobial and antioxidant activities

机译:通过多组分反应合成新的吡唑衍生物并评估其抗菌和抗氧化活性

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摘要

This work describes a facile synthesis and characterization of a new series of pyrazole containing pyrimidine, 1,4-dihydropyridine, and imidazole derivatives using substituted 4-formylpyrazole as a key intermediate via multicomponent reaction sequence. The structures of these unknown compounds were elucidated by IR, H-1 NMR, C-13 NMR, LC-MS, and elemental analysis. The synthesized products were screened for their in vitro antimicrobial and antioxidant properties. Among the tested 3-(3,4-dihalophenyl)-1-phenyl-1H-pyrazol-4-yl, incorporated acetyl dihydropyrimidine compounds exhibited promising antimicrobial activity and DPPH radical scavenging activity with levels of inhibition at 89.4 and 83.3 %, respectively.
机译:这项工作描述了新的一系列含有嘧啶,1,4-二氢吡啶和咪唑衍生物的吡唑的合成和表征,该衍生物通过多组分反应序列使用取代的4-甲酰基吡唑作为关键中间体。通过IR,H-1 NMR,C-13 NMR,LC-MS和元素分析阐明了这些未知化合物的结构。筛选合成产物的体外抗菌和抗氧化性能。在测试的3-(3,4-二卤苯基)-1-苯基-1H-吡唑-4-基中,掺入的乙酰基二氢嘧啶化合物显示出有希望的抗菌活性和DPPH自由基清除活性,其抑制水平分别为89.4%和83.3%。

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