Synthetic approaches towards the sulfonamide substituted-4,5-diaryl-4H-1,2,4-triazole-3-thiones
✍ Scribed by Latifeh Navidpour; Mohsen Amini; Abbas Shafiee
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2007
- Tongue
- English
- Weight
- 508 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
magnified image
A new series of 3‐alkylthio‐4,5‐diaryl‐4__H__‐1,2,4‐triazoles having a SO~2~NH~2~ substituent in the para‐position on one of the aryl rings (19/25) were prepared starting from the appropriate benzoic acid hydrazides (15/21). Reaction of the corresponding hydrazides with the appropriate isothiocyanates yielded 16/22, which were cyclized in basic media to give 4,5‐diaryl‐2,4‐dihydro‐3__H__‐1,2,4‐triazole‐3‐thiones 17/23. Alkylation of 17/23 afforded the alkylthio compounds 18/24. Final debenzylation was achieved with concentrated sulfuric acid to give the target sulfonamides 19/25.
📜 SIMILAR VOLUMES
## Abstract magnified image Various 4‐amino‐2,3‐dihydro‐4__H__‐triazoles with aromatic, aliphatic and heterocyclic substituents at the C(5) position were synthesized from corresponding esters and thiocarbohydrazide. This method allows the synthesis these heterocycles in a short time and at reduced