Nickel-catalyzed Chan–Lam coupling: an efficient route to N-arylated 2-aminobenzothiazoles under ambient conditions

IF 4.6 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
RSC Advances Pub Date : 2025-10-16 DOI:10.1039/D5RA06530E
Rose Mary Philip, P. S. Devi and Gopinathan Anilkumar
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引用次数: 0

Abstract

A nickel-catalyzed C–N coupling of 2-aminobenzothiazoles and aryl boronic acids under mild reaction conditions is disclosed. The reaction afforded N-arylated 2-aminobenzothiazoles in the presence of a Ni/4,4′-dOMebpy catalytic system under open-air conditions. The method encompasses a wide range of applicable substrates, including aryl boronic acids and 2-aminobenzothiazoles, affording the corresponding C–N coupled products in moderate to good yields in short reaction times.

Abstract Image

镍催化的Chan-Lam偶联:环境条件下n -芳基化2-氨基苯并噻唑的有效途径
在温和的反应条件下,镍催化2-氨基苯并噻唑和芳基硼酸的C-N偶联。在露天条件下,在Ni/4,4 ' -dOMebpy催化体系的存在下,得到n-芳基化的2-氨基苯并噻唑。该方法涵盖了广泛的适用底物,包括芳基硼酸和2-氨基苯并噻唑,在短的反应时间内以中等到良好的产率提供相应的C-N偶联产物。
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来源期刊
RSC Advances
RSC Advances chemical sciences-
CiteScore
7.50
自引率
2.60%
发文量
3116
审稿时长
1.6 months
期刊介绍: An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.
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