Nickel-Catalyzed N-Arylation of Amides with (Hetero)aryl Electrophiles using a DBU/NaTFA Dual-Base System
Keyword(s):
System A
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The first nickel-catalyzed N-arylation of amides with (hetero)aryl (pseudo)halides employing an organic amine base is described. When using Ni(COD)2/CyPAd-DalPhos catalyst mixtures in combination with DBU/NaTFA as a dual-base system, a diversity of (hetero)aryl chloride, bromide, tosylate, and mesylate electrophiles were successfully cross-coupled with structurally varied primary amides, as well as a selection of secondary amide, lactam, and oxazolidone nucleophiles.