苯并[4',5']咪唑并[2',1':6,1]吡啶并[2,3-d]嘧啶:过去与现在

IgMin Research Pub Date : 2023-11-16 DOI:10.61927/igmin113
Harutyunyan Aa
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引用次数: 0

摘要

本研究考虑了基于取代苯并咪唑的杂环化作用构建杂环苯并[4',5']咪唑并[2',1':6,1]吡啶并[2,3-d]嘧啶体系的合成方法,以及基于 2,4,6-三取代嘧啶基-5-丙酸的新替代策略。后一种方法已被证明是对之前描述的方法的成功补充,因为它可以绕过与使用取代的苯并咪唑相关的重大限制,并允许在杂环的不同位置引入其他方法无法获得的功能取代基。本文概述了有关这种杂环系统的衍生物及其生物特性的现有信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Benzo[4’,5’]imidazo[2’,1’:6,1]pyrido[2,3-d]pyrimidines: Past and Present
Synthetic approaches to the construction of the heterocyclic benzo[4’,5’]imidazo[2’,1’:6,1]pyrido[2,3-d]pyrimidine system based on heterocyclizations of substituted benzimidazoles and a new alternative strategy based on 2,4,6-trisubstituted pyrimidinyl-5-propanoic acids are considered. The latter method has been shown to be a successful addition to previously described methods, since it allows one to bypass the significant limitations associated with the use of substituted benzimidazoles and allows the introduction of functional substituents at different positions of the heterocycle that are inaccessible by other methods. The available information on derivatives of this heterocyclic system and their biological properties is summarized.
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