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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720705Generated: October 28, 2026

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

https://huagongshe.com/reaction/720705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
ReactantHCID 21894667HCID 21894667—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product4-[5-(4-Fluoro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamideHCID 1023678461%

Reaction Steps

N-(1-ethoxy-ethylidene)-4-fluoro-benzamide 438 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-(4-fluoro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamide (424 mg, yield: 61%) was obtained as a solid phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135572B2
Source datasetuspto-grants-2006_11
ORD IDord-a28a0ca93aa244f6a231e03cb0ae90c9
Source noteuspto-grants-2006_11