Copper-Catalyzed Intermolecular Oxidative Cyclization of Haloalkynes: Synthesis of 2-Halo-substituted Imidazo[1,2-a]pyridines, Imidazo[1,2-a]pyrazines and Imidazo[1,2-a]pyrimidines

被引:112
作者
Gao, Yang [1 ]
Yin, Meizhou [1 ]
Wu, Wanqing [1 ]
Huang, Huawen [1 ]
Jiang, Huanfeng [1 ]
机构
[1] S China Univ Technol, Sch Chem & Chem Engn, Guangzhou 510640, Guangdong, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
aerobic oxidative cyclization; Cu-catalyzed reaction; diamination; haloalkynes; imidazopyridines; PERIPHERAL BENZODIAZEPINE-RECEPTOR; ONE-POT SYNTHESIS; TERMINAL ALKYNES; INTRAMOLECULAR DIAMINATION; STEREOSELECTIVE-SYNTHESIS; SONOGASHIRA REACTIONS; DIRECT ALKYNYLATION; COUPLING REACTIONS; SUZUKI-TYPE; DIFUNCTIONALIZATION;
D O I
10.1002/adsc.201300157
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
An efficient copper-catalyzed method for the synthesis of 2-haloimidazopyridines with aminopyridines and haloalkynes using molecular oxygen as oxidant in a one-pot manner has been developed. In this process, the reaction appears to be very general and suitable for the construction of a variety of 2-halo-substituted imidazopyridines, imidazopyrazines and imidazopyrimidines. The intermolecular oxidative diamination of haloalkynes was achieved for the first time. Importantly, the mild reaction conditions and the efficient conversion of the alkyl-substituted haloalkynes are great improvements over the existing methods. Moreover, the resultant 2-haloimidazo[1,2-a]pyridines could be efficiently converted to other functionalized imidazopyridine products via substitution, coupling reactions and other transformations, which further indicates potential applications of this method in synthetic and pharmaceutical chemistry.
引用
收藏
页码:2263 / 2273
页数:11
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