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Mendeleev Communications, 2025, Volume 35, Issue 2, Pages 214–216
DOI: https://doi.org/10.71267/mencom.7609
(Mi mendc1359)
 

Communications

Mild cuprous halide mediated direct C3 monohalogenation of indoles

X. Hea, J. Suib, J. Xua, Z. Wanga, T. Yuana, D. Liua, L. Wanga, Q. Zhuc

a School of Chemical and Pharmaceutical Engineering, Changzhou Vocational Institute of Engineering, 213164 Changzhou, P.R. China
b Nanjing Customs Testing Center for Dangerous Goods and Packaging, 213100 Changzhou, China
c Department of Medicinal Chemistry, China Pharmaceutical University, 210009 Nanjing, China
References:
Abstract: Treatment of indoles with cuprous halide–N-fluorobenzenesulfonimide system in MeCN at room temperature affords the corresponding C3-halogenated derivatives. Cuprous halide acts as a dual-function reagent serving both as the halogen source and the promoter.
Keywords: indole derivatives, halogenation, cuprous halide, N-fluorobenzenesulfonimide, mild conditions.
Received: 02.09.2024
Accepted: 16.10.2024
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (5.1 Mb)


Citation: X. He, J. Sui, J. Xu, Z. Wang, T. Yuan, D. Liu, L. Wang, Q. Zhu, “Mild cuprous halide mediated direct C3 monohalogenation of indoles”, Mendeleev Commun., 35:2 (2025), 214–216
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