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自2010年以来生物活性吡咯衍生物的绿色合成 多相催化剂

Green Synthesis of Bioactive Pyrrole Derivatives Heterogeneous Catalysts Since 2010.

作者信息

Amina Berrichi, Redouane Bachir

机构信息

Laboratory of Catalysis and Synthesis in Organic Chemistry, University of Tlemcen, BP 119, 13000, Tlemcen, Algeria.

University of Ain Temouchent, BP 284, 46000, Ain Temouchent, Algeria.

出版信息

Curr Top Med Chem. 2025;25(5):461-492. doi: 10.2174/0115680266307696240708115422.

Abstract

Pyrrole derivatives are known as building blocks for the synthesis of biological compounds and pharmaceutical drugs. Several processes were employed to synthesize pyrroles, including Hantzsch, Paal-Knorr, and cycloaddition of dicarbonyl compounds reaction. Using catalysts like nanoparticles, metal salts, and heterogeneous ones was necessary to obtain the targeted pyrrole structure. Also, to afford more active pyrrole compounds, heterocyclic molecules such as imidazole or other rings were used in the synthesis as amines. This review presents heterogeneous catalysts since 2010 for the green synthesis of bioactive pyrroles in a one-pot multi-component reaction. Additionally, each synthetic method included a demonstration of the suggested mechanisms. Diakylacetylenedicarboxylate, dicarbonyl group, amines, furans, and acetylene group are consolidated to yield biological pyrroles through the heterogeneous catalysts. Finally, various pyrrole-performed activities were displayed, such as antibacterial, anti-inflammatory, analgesic, and other significant activities.

摘要

吡咯衍生物是合成生物化合物和药物的基础材料。人们采用了多种方法来合成吡咯,包括汉茨希法、帕尔-克诺尔法以及二羰基化合物的环加成反应。使用纳米颗粒、金属盐和多相催化剂等催化剂对于获得目标吡咯结构是必要的。此外,为了得到更具活性的吡咯化合物,在合成过程中使用了咪唑等杂环分子或其他环作为胺类。本综述介绍了自2010年以来用于一锅多组分反应绿色合成生物活性吡咯的多相催化剂。此外,每种合成方法都包括对所建议机理的说明。通过多相催化剂将二烷基乙炔二羧酸酯、二羰基基团、胺类、呋喃和乙炔基团结合起来,以生成生物吡咯。最后,展示了各种吡咯所具有的活性,如抗菌、抗炎、镇痛和其他重要活性。

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