Volume 24, Issue 1 pp. 127-142
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On Triazoles. VI. The acylation of 5-amino-1,2,4-triazoles

József Reiter

József Reiter

EGIS Pharmaceuticals, H-1475 Budapest, P. O. Box 100, Hungary

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László Pongó

László Pongó

EGIS Pharmaceuticals, H-1475 Budapest, P. O. Box 100, Hungary

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Péter Dvortsák

Péter Dvortsák

Institute for Drug Research, H-1325 Budapest, P. O. Box 82, Hungary

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First published: January/February 1987
Citations: 20

For part V. see: J. Reiter, L. Pongó, T. Somorai and P. Dvortsák, J. Heterocyclic Chem., 23, 401 (1986).

Abstract

The isomeric and tautomeric structure of I and II type monoacylated 5-amino-1,2,4-triazole derivatives was studied with the help of their ir, uv, pmr and cmr spectra as well as model compounds prepared for this purpose. It was stated that the structure of the I type ring-acylated derivatives is 2o and those of their II type isomers is 5a.

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