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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376079Generated: November 3, 2026

Water → 4-[5-(3-Chloro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamide

https://huagongshe.com/reaction/1376079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
ReactantN-(1-ethoxy-ethylidene)-3-chloro-benzamideHCID 21894665—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product4-[5-(3-Chloro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamideHCID 1012601071%

Reaction Steps

N-(1-ethoxy-ethylidene)-3-chloro-benzamide 472 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-[5-(3-chloro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamide (517 mg, yield: 71%) was obtained as a solid phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169929B2
Source datasetuspto-grants-2007_01
ORD IDord-f8a69c8da7f148f093052b456c5a63f6
Source noteuspto-grants-2007_01