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DNA 偶联芳基溴化物与芳基胺之间温和高效的钯介导 C-N 交叉偶联反应。

Mild and Efficient Palladium-Mediated C-N Cross-Coupling Reaction between DNA-Conjugated Aryl Bromides and Aromatic Amines.

机构信息

Centro de Investigación Lilly, S. A. , 28108 Alcobendas, Madrid , Spain.

出版信息

ACS Comb Sci. 2019 Feb 11;21(2):69-74. doi: 10.1021/acscombsci.8b00142. Epub 2019 Jan 10.

DOI:10.1021/acscombsci.8b00142
PMID:30615417
Abstract

DNA-encoded library technology (ELT) has emerged in the pharmaceutical industry as a powerful tool for hit and lead generation. Over the last 10 years, a number of DNA-compatible chemical reactions have been published and used to synthesize libraries. Among the most commonly used reactions in medicinal chemistry is the C-N bond formation, and its application to DNA-encoded library technology affords an alternative approach to identify high-affinity binders for biologically relevant protein targets. Herein we report a newly developed Pd-promoted C-N cross coupling reaction between DNA-conjugated aryl bromides and a wide scope of arylamines in good to excellent yields. The mild reaction conditions should facilitate the synthesis of novel DNA-encoded combinatorial libraries.

摘要

DNA 编码文库技术 (ELT) 在制药行业中已成为一种强大的工具,可用于命中和先导化合物的生成。在过去的 10 年中,已经发表并使用了许多与 DNA 兼容的化学反应来合成文库。在药物化学中最常用的反应之一是 C-N 键形成,其在 DNA 编码文库技术中的应用为鉴定生物相关蛋白靶标高亲和力结合物提供了另一种方法。在此,我们报道了一种新开发的 Pd 促进的 DNA 连接的芳基溴化物与广泛的芳基胺之间的 C-N 交叉偶联反应,收率良好至优秀。温和的反应条件应有利于新型 DNA 编码组合文库的合成。

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