Ni-Catalyzed C-H Arylation of Oxazoles and Benzoxazoles Using Pharmaceutically Relevant Aryl Chlorides and Bromides

被引:29
作者
Larson, Helen [1 ]
Schultz, Danielle [2 ]
Kalyani, Dipannita [1 ,3 ]
机构
[1] St Olaf Coll, Dept Chem, 1520 St Olaf Ave, Northfield, MN 55057 USA
[2] Merck & Co Inc, Proc Res & Dev, Rahway, NJ 07065 USA
[3] Merck & Co Inc, Discovery Chem, Kenilworth, NJ 07033 USA
关键词
HIGH-THROUGHPUT EXPERIMENTATION; NICKEL CATALYSIS; CARBON-HYDROGEN; BOND FORMATION; AZOLES; PALLADIUM; FUNCTIONALIZATION; HETEROARENES; MECHANISM; ALKENYLATION;
D O I
10.1021/acs.joc.9b02094
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
This manuscript details the development of the nickel-catalyzed arylation of oxazoles and benzoxazoles with aryl halides. A series of aryl, heteroaryl, and druglike electrophiles relevant to pharmaceutical applications were surveyed. The desired arylated products were obtained in synthetically useful yields using electronically and structurally varied aryl halides. The use of microscale high-throughput experimentation was essential for both the rapid identification of optimal reaction parameters and the investigation of the aryl halide scope.
引用
收藏
页码:13092 / 13103
页数:12
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