C3-Heteroarylation of Indoles via Cu(II)-Catalyzed Aminocupration and Subsequent Nucleophilic Addition of o-Alkynylanilines

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC Journal of Organic Chemistry Pub Date : 2025-02-23 DOI:10.1021/acs.joc.5c00007
Amitava Rakshit, Kyeongwon Moon, Pargat Singh, In Su Kim
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Abstract

Transition-metal-catalyzed aminometalation of o-alkynylanilines is a promising pathway for the synthesis of C3-functionalized indoles. Herein, we describe the Cu(II)-catalyzed site-selective C3-heteroarylation of indoles from o-alkynylanilines and quinoline N-oxides. A plausible reaction mechanism involving the aminocupration of o-alkynylanilines followed by the nucleophilic addition of Cu(II)-indolyl complexes to quinoline N-oxides was proposed. Post-transformations of the generated C3-heteroarylated indoles demonstrated the broad applicability of the developed method.

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Cu(II)催化氨基接种对吲哚的c3 -异芳基化反应及邻烷基苯胺的亲核加成反应
过渡金属催化的邻炔基苯胺氨甲基化反应是合成 C3 功能化吲哚的一条很有前景的途径。在此,我们介绍了 Cu(II) 催化的邻炔基苯胺和喹啉 N-氧化物对吲哚的位点选择性 C3-异芳香化反应。提出了一个合理的反应机理,即邻炔基苯胺胺化后,Cu(II)-吲哚络合物与喹啉 N-氧化物发生亲核加成反应。生成的 C3-杂芳基化吲哚的后转化证明了所开发方法的广泛适用性。
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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
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