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Synlett 2018; 29(14): 1875-1880
DOI: 10.1055/s-0037-1609558
DOI: 10.1055/s-0037-1609558
letter
Palladium-Catalyzed Arylation of Aromatic Amides Directed by a [4-Chloro-2-(1H-pyrazol-1-yl)phenyl]amine Auxiliary
We gratefully thank the National Natural Science Foundation of China (Project Nos. 21476074 and 21676088) for financial support.
Further Information
Publication History
Received: 28 April 2018
Accepted after revision: 14 June 2018
Publication Date:
20 July 2018 (online)
◊ Ya-Hua Hu and Zhi Xu are equal first authors.
Abstract
A palladium-catalyzed ortho-arylation of aromatic amides directed by [4-chloro-2-(1H-pyrazol-1-yl)phenyl]amine as a bidentate auxiliary has been established. The reaction is characterized by normal working conditions, a broad substrate scope, and a wide functional-group tolerance. In particular, the protocol is compatible with highly sterically demanding ortho-substituted anilides and aryl iodide partners, with good yields.
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0037-1609558.
- Supporting Information
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For selected heteroarene-directed arylations, see:
For selected functional groups directed arylation: