TfOH-catalyzed regioselective N2-alkylation of indazoles with diazo compounds
Hangli He1,2, Jingyu Yan2, Jingru Jin1,2
1Pharmaceutical Research Institute, Wuhan Institute of Technology, Wuhan 430205, China. skytacle@139.com.
Abstract:
Selective alkylation of indazoles is still a highly challenging topic in chemistry and the synthesis of important molecules. Herein, a novel highly selective N2-alkylation of indazoles with diazo compounds is described in the presence of TfOH. Unlike the traditional metal- and base-catalysed version, this protocol highlights the regioselectivity of alkylation of indazoles and a metal-free catalysis system, affording N2-alkylated products in good to excellent yields with high regioselectivity (N2/N1 up to 100/0) and excellent functional group tolerance. Furthermore, a gram scale synthesis was conducted successfully to give rise to the corresponding products. Mechanistic studies through control experiments provide plausible mechanistic proposals.
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