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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720712Generated: October 30, 2026

Water → HCID 10286770, compound

https://huagongshe.com/reaction/720712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
ReactantHCID 21894689HCID 21894689—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 10286770HCID 1028677070%

Reaction Steps

N-(1-ethoxy-ethylidene)-3-methoxy-benzamide 462 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-methoxy-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamide (503 mg, yield: 70%) was obtained as a solid phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135572B2
Source datasetuspto-grants-2006_11
ORD IDord-bf5995cf0b1c4c83b69af0c1e78da602
Source noteuspto-grants-2006_11