Literature DB >> 16292870

Mild and practical method for the alpha-arylation of nitriles with heteroaryl halides.

Artis Klapars1, Jacob H Waldman, Kevin R Campos, Mark S Jensen, Mark McLaughlin, John Y L Chung, Raymond J Cvetovich, Cheng-Yi Chen.   

Abstract

[reaction: see text] A mild and transition-metal-free method for the alpha-arylation of aliphatic nitriles with activated heteroaryl halides was developed using NaHMDS or KHMDS as base at ambient temperature. The key to the success of this method is generation of the nitrile anion in the presence of the heteroaryl halide. The method is applicable to both primary and secondary carbonitriles and a wide range of heteroaryl halides. Selective monoarylation was observed with primary carbonitriles. The operational simplicity and the mild reaction conditions add to the value of this method as a practical alternative to the preparation of alpha-heteroaryl carbonitriles.

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Year:  2005        PMID: 16292870     DOI: 10.1021/jo051737f

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  2 in total

1.  Novel GlyT1 inhibitor chemotypes by scaffold hopping. Part 1: development of a potent and CNS penetrant [3.1.0]-based lead.

Authors:  Carrie K Jones; Douglas J Sheffler; Richard Williams; Sataya B Jadhav; Andrew S Felts; Ryan D Morrison; Colleen M Niswender; J Scott Daniels; P Jeffrey Conn; Craig W Lindsley
Journal:  Bioorg Med Chem Lett       Date:  2014-01-13       Impact factor: 2.823

2.  Synthesis and late-stage functionalization of complex molecules through C-H fluorination and nucleophilic aromatic substitution.

Authors:  Patrick S Fier; John F Hartwig
Journal:  J Am Chem Soc       Date:  2014-07-01       Impact factor: 15.419

  2 in total

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