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Recent Progress in Synthetic Chemistry and Biological Activities of Pyrimido[ 4,5-b] Quinoline Derivatives (Part III)
Mini-Reviews in Organic Chemistry ( IF 2.3 ) Pub Date : 2023-07-20 , DOI: 10.2174/1570193x20666230626101436
Moustafa A. Gouda 1, 2 , Ameen A. Abu-Hashem 3 , Tahah A. Ameen 3 , Mohammed A. Salem 4, 5 , Ateyatallah Aljuhan 6
Affiliation  

Amongst heterocyclic compounds, quinoline and pyrimidine are advantaged scaffolds that appear as significant assembly motifs for the development of new drug entities. Moreover, quinolinepyrimidine- inspired hybrids have a number of biological characteristics that are known. In addition, many pyrimido[4,5-b]quinoline ring systems (PyQs4,5-b), specifically concerning medicinal chemistry, have been reported over the past decade. The synthesis of (PyQs4,5-b) using barbituric acid, thiobarbituric acid, pyrimidine, and their derivatives is presented in this review. The preparation of PyQs4,5-b was clarified through the following chemical reactions: Friedländer, Vilsmeier-Haack formylation, Hantzsch-like reaction, and one-pot three-component reaction.

中文翻译:

嘧啶[4,5-b]喹啉衍生物的合成化学及生物活性研究进展(下)

在杂环化合物中,喹啉和嘧啶是有利的支架,它们似乎是新药物实体开发的重要组装基序。此外,喹啉嘧啶启发的杂种具有许多已知的生物学特征。此外,在过去的十年中,已经报道了许多嘧啶并[4,5-b]喹啉环系统(PyQs4,5-b),特别是与药物化学有关的系统。本综述介绍了使用巴比妥酸、硫代巴比妥酸、嘧啶及其衍生物合成 (PyQs4,5-b)。PyQs4,5-b的制备通过以下化学反应阐明:Friedländer、Vilsmeier-Haack甲酰化、类Hantzsch反应和一锅三组分反应。
更新日期:2023-07-20
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