6533b85ffe1ef96bd12c27b9
RESEARCH PRODUCT
1,2,4-Triazoles. Improved synthesis of 5-substituted 4-amino-3-mer-cato-(4H)-1,2,4-triazoles and a facile route to 3,6-disubstituted 1,2,4-triazolo[3,4-b][1,3,4]thiadiazoles
Ilaria LamprontiGiancarlo FurnáDaniele SimoniFrancesco Paolo Invidiatasubject
chemistry.chemical_classificationThiocarbohydrazidechemistry.chemical_compoundThiadiazoleschemistryMelting temperatureCarboxylic acidOrganic ChemistryRing (chemistry)Medicinal chemistrydescription
The reaction of thiocarbohydrazide with carboxylic acids at the melting temperature allows an improved preparation of the S-substituted 4-amino-3-mercapto-1,2,4-triazole heterocycles. The crude 4-amino-5-mercapto-1,2,4-triazoles react easily with carboxylic acids or carboxylic acid chlorides to afford the 1,2,4-triazolo[3,4-fc][1,3,4]thiadiazole ring system.
year | journal | country | edition | language |
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1997-07-01 | Journal of Heterocyclic Chemistry |