Issue 9, 1998

Reactions with 3-Amino-5-trifluoromethyl[1,2,4]-triazole: A Convenient Route to Fluorinated Triazolo[1,5-c]thiadiazine, Triazolo[1,5-a]triazine, Thiazoles and Thiadiazoles

Abstract

The reaction of 3-amino-5-trifluoromethyl[1,2,4]triazole with carbon disulfide or phenyl isothiocyanate followed by heterocyclization with haloketones, haloesters and hydrazonoyl halides has been utilized for the synthesis of the title compounds; chemical and spectroscopic evidence for the suggested structures of the new compounds and a sequence leading to their formation are discussed.

Article information

Article type
Paper

J. Chem. Res. (S), 1998, 536-537

Reactions with 3-Amino-5-trifluoromethyl[1,2,4]-triazole: A Convenient Route to Fluorinated Triazolo[1,5-c]thiadiazine, Triazolo[1,5-a]triazine, Thiazoles and Thiadiazoles

H. F. Zohdi, J. Chem. Res. (S), 1998, 536 DOI: 10.1039/A802034E

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