Synthesis 1988; 1988(7): 553-555
DOI: 10.1055/s-1988-27637
communication
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Synthesis of N-(5-Aminopyrazol-3-yl)amino and N(5-Amino-1,2,4-triazol-3-yl)amino Acids

Masataka Yokoyama* , Katsushi Kumata, Hidehiko Noro, Akemi Kogo
  • *Department of Chemistry, Faculty of Science, Chiba University, Yayoicho, Chiba City 260, Japan
Further Information

Publication History

Publication Date:
18 September 2002 (online)

Some N-(5-aminopyrazol-3-yl) and N-(5-amino-1,2,4-triazol-3-yl) derivatives of amino acids or dipeptides are synthesized in good yields from the reaction of α-(aminocarbonyl)-α-cyanoketene dithioacetals with amino acid or dipeptide tert-butyl esters and cyclocondensation of the resultant α-(aminocarbonyl)-α-cyanoketene S,N-acetals [N-(2-aminocarbonyl-2-cyano-1-methylthioethenyl)amino acid derivatives] with hydrazine hydrate.

    >