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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720708Generated: October 29, 2026

Water → 4-(3-Methyl-5-p-toly-[1,2,4]triazole-1-yl)-benzenesulfonamide

https://huagongshe.com/reaction/720708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
ReactantN-(1-ethoxy-ethylidene)-4-methyl-benzamideHCID 21894679—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product4-(3-Methyl-5-p-toly-[1,2,4]triazole-1-yl)-benzenesulfonamideHCID 1028657568%

Reaction Steps

N-(1-ethoxy-ethylidene)-4-methyl-benzamide 429 mg (2.09 mmol) was dissolved in a mixed solvent of dichloromethane 20 ml and methanol 10 ml, and 4-hydrazinobenzenesulfonamide hydrochloride 515 mg (2.23 mmol) was added to the solution. Then, triethylamine 0.35 ml (2.51 mmol) was slowly added dropwise at room temperature for 10 minutes and stirred for 8 hours. After completing the reaction, water 20 ml was added to the reacting solution and extracted two times with dichloromethane, and then, the collected organic layer was washed with saturated brine. The organic layer was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure, and the resulting product was re-crystallized in acetone and hexane phase. As a result, 4-(3-methyl-5-p-toly-[1,2,4]triazole-1-yl)-benzenesulfonamide (467 mg, yield: 68%) was obtained as a solid phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135572B2
Source datasetuspto-grants-2006_11
ORD IDord-e9f5c0fb64fc4665bec67c064484f354
Source noteuspto-grants-2006_11