苯并咪唑文库的氧化环化方法

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Eric P. Arnold, Prolay K. Mondal, Daniel C. Schmitt*
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引用次数: 3

摘要

介绍了一种苯胺平行合成苯并咪唑的有效方法。改变苯并咪唑N1和C2载体的文库方法已经建立;然而,C4-C7的变异传统上依赖于1,2-二苯胺构建块,提供有限的化学空间覆盖。我们已经开发了一种脒形成/氧化环化序列,使苯胺作为平行形式生成苯并咪唑C4-C7 SAR的多样性集。通过PIDA或cu介导氧化获得N-H和n -烷基苯并咪唑,实现了脒环化。该库协议现已在四个药物化学项目中用于模拟生产。此外,由氨基吡啶合成氮杂-苯并咪唑是通过类似的序列实现的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Oxidative Cyclization Approach to Benzimidazole Libraries

Oxidative Cyclization Approach to Benzimidazole Libraries

An efficient approach to the parallel synthesis of benzimidazoles from anilines is described. Library approaches to vary the N1 and C2 vectors of benzimidazoles are well established; however, C4–C7 variation has traditionally relied on 1,2-dianiline building blocks, providing limited chemical space coverage. We have developed an amidine formation/oxidative cyclization sequence that enables anilines as a diversity set for benzimidazole C4–C7 SAR generation in parallel format. The amidine annulation was achieved using PIDA or Cu-mediated oxidation to access both N–H and N–alkyl benzimidazoles. This library protocol has now been utilized for analog production in four medicinal chemistry projects. Additionally, the synthesis of aza-benzimidazoles from aminopyridines was achieved via an analogous sequence.

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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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