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Nickel-Catalyzed Amination of Aryl Chlorides and Sulfamates in 2-Methyl-THF

[Image: see text] The nickel-catalyzed amination of aryl O-sulfamates and chlorides using the green solvent 2-methyl-THF is reported. This methodology employs the commercially available and air-stable precatalyst NiCl(2)(DME), is broad in scope, and provides access to aryl amines in synthetically us...

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Detalles Bibliográficos
Autores principales: Fine Nathel, Noah F., Kim, Junyong, Hie, Liana, Jiang, Xingyu, Garg, Neil K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165539/
https://www.ncbi.nlm.nih.gov/pubmed/25243095
http://dx.doi.org/10.1021/cs501045v
Descripción
Sumario:[Image: see text] The nickel-catalyzed amination of aryl O-sulfamates and chlorides using the green solvent 2-methyl-THF is reported. This methodology employs the commercially available and air-stable precatalyst NiCl(2)(DME), is broad in scope, and provides access to aryl amines in synthetically useful yields. The utility of this methodology is underscored by examples of gram-scale couplings conducted with catalyst loadings as low as 1 mol % nickel. Moreover, the nickel-catalyzed amination described is tolerant of heterocycles and should prove useful in the synthesis of pharmaceutical candidates and other heteroatom-containing compounds.