Literature DB >> 15527255

Easy access to 3- or 5-heteroarylamino-1,2,4-triazines by S(N)Ar, S(N)H, and palladium-catalyzed N-heteroarylations.

Ethel Garnier1, Jérôme Audoux, Eric Pasquinet, Franck Suzenet, Didier Poullain, Bruno Lebret, Gérald Guillaumet.   

Abstract

In this paper, N-arylations between two heteroaryl compounds were studied. Conditions were found to generate selectively either 3- or 5-heteroarylamino-1,2,4-triazines by investigating anionic processes (use of bases such as 2,2',6,6'-tetramethylpiperidine/tBuOK/nBuLi) or Pd-catalyzed N-arylations [Pd(OAc)(2), xantphos]. These methods were successfully applied to a wide variety of heteroarylamines and allowed us to pursue our work on fused polynitrogen compounds synthesis.

Entities:  

Year:  2004        PMID: 15527255     DOI: 10.1021/jo0490898

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


  1 in total

1.  Amination of nitroazoles--a comparative study of structural and energetic properties.

Authors:  Xiuxiu Zhao; Cai Qi; Lubo Zhang; Yuan Wang; Shenghua Li; Fengqi Zhao; Siping Pang
Journal:  Molecules       Date:  2014-01-14       Impact factor: 4.411

  1 in total

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