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一些吡唑啉酮化合物绿色合成的催化及多组分反应及其作为抗菌剂的评价

Catalytic and Multicomponent Reactions for Green Synthesis of Some Pyrazolone Compounds and Evaluation as Antimicrobial Agents.

作者信息

Ali Hazim M, El-Ossaily Yasser A, Metwally Saoud A, Althobaiti Ibrahim O, Altaleb Hamud A, Naffea Yousra A, Tolba Mahmoud S

机构信息

Department of Chemistry,College of Science, Jouf University, Sakaka 72341, Aljouf, Saudi Arabia.

Chemistry Department, Faculty of Science, Assiut University, Assiut 71516, Egypt.

出版信息

ACS Omega. 2022 Aug 8;7(33):29142-29152. doi: 10.1021/acsomega.2c03070. eCollection 2022 Aug 23.

DOI:10.1021/acsomega.2c03070
PMID:36033712
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9404472/
Abstract

A green synthetic approach and facile method was developed to produce pyrazole compounds () by the reaction of ethyl acetoacetate (), hydrazines (), and catalytic imidazole () in aqueous media. 4-Dicyanomethylene-2-pyrazoline-5-one derivatives () were synthesized through the reaction of 2-pyrazoline-5-one derivatives () with tetracyanoethylene (TCE) () by using catalytic imidazole () in an aqueous medium. Moreover, the 4-dicyanomethylene derivative () was obtained via treatment of 1-phenyl-3,5-pyrazolidinedione (1) with TCE (). The spiropyrazoleoxirane derivatives ( and ) were prepared by treating the precursor 4-dicyanomethylene-2-pyrazoline-5-one derivative () with hydrogen peroxide in various polar solvents under alkaline conditions. The spiropyrazole oxirane derivative () was used as a precursor for the design of functionalized pyrazolone derivatives ( and , ). The chemical structure of the novel designed derivatives was ascertained based on elemental analyses, mp, thin-layer chromatography, and spectral analyses. Furthermore, some of the synthesized derivatives were examined against different pathogenic bacterial and fungal strains. Their results demonstrated that some of them revealed notable antimicrobial activities.

摘要

开发了一种绿色合成方法和简便方法,通过乙酰乙酸乙酯、肼和催化量的咪唑在水介质中的反应来制备吡唑化合物。通过2-吡唑啉-5-酮衍生物与四氰基乙烯(TCE)在水介质中使用催化量的咪唑反应,合成了4-二氰基亚甲基-2-吡唑啉-5-酮衍生物。此外,通过用TCE处理1-苯基-3,5-吡唑烷二酮(1)得到4-二氰基亚甲基衍生物。通过在碱性条件下在各种极性溶剂中用过氧化氢处理前体4-二氰基亚甲基-2-吡唑啉-5-酮衍生物来制备螺吡唑环氧乙烷衍生物。螺吡唑环氧乙烷衍生物用作设计功能化吡唑啉酮衍生物的前体。基于元素分析、熔点、薄层色谱和光谱分析确定了新设计衍生物的化学结构。此外,对一些合成衍生物针对不同的致病细菌和真菌菌株进行了检测。它们的结果表明其中一些显示出显著的抗菌活性。

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