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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376080Generated: November 4, 2026

Water → HCID 10309572, compound

https://huagongshe.com/reaction/1376080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
ReactantHCID 21894682HCID 21894682—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 10309572HCID 1030957266.1%

Reaction Steps

N-(1-ethoxy-ethylidene)-3-bromo-benzamide 565 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 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-bromo-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamide (543 mg, yield: 66%) was obtained as a solid phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169929B2
Source datasetuspto-grants-2007_01
ORD IDord-9f7716c7e18a4b0291cdd9865d4c675d
Source noteuspto-grants-2007_01