Synlett 2017; 28(05): 589-592
DOI: 10.1055/s-0036-1588125
letter
© Georg Thieme Verlag Stuttgart · New York

Mechanochemical Synthesis of Substituted 4H-3,1-Benzoxazin-4-ones, 2-Aminobenzoxazin-4-ones, and 2-Amino-4H-3,1-benzothiazin-4-ones Mediated by 2,4,6-Trichloro-1,3,5-triazine and Triphenylphosphine

Authors

  • Mookda Pattarawarapan*

    Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand   Email: mookdap55@gmail.com
  • Sirawit Wet-osot

    Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand   Email: mookdap55@gmail.com
  • Dolnapa Yamano

    Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand   Email: mookdap55@gmail.com
  • Wong Phakhodee

    Department of Chemistry and Center of Excellence for Innovation in Chemistry, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand   Email: mookdap55@gmail.com
Further Information

Publication History

Received: 14 October 2016

Accepted after revision: 27 November 2016

Publication Date:
12 December 2016 (online)


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Abstract

A mild and convenient approach for the synthesis of 2-substituted 4H-3,1-benzoxazin-4-ones, 2-aminobenzoxazin-4-ones, and 2-amino-4H-3,1-benzothiazin-4-ones under solvent-assisted grinding is reported. In the presence of 2,4,6-trichloro-1,3,5-triazine and catalytic triphenylphosphine, cyclodehydration of N-substituted anthranilic acid derivatives proceeded rapidly within minutes at room temperature. The products were also obtained in good to excellent yields by using minimal amounts of solvent and inexpensive reagents.

Supporting Information