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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396740Generated: October 29, 2026

4-Hydrazinylbenzenesulfonamide hydrochloride → 4-[5-[4-(2-Furyl)-3-methylphenyl]-3-(trifluoromethyl)-1H-pyrazol-1-yl]-phenylsulfonamide

https://huagongshe.com/reaction/396740

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
Reactant4,4,4-Trifluoro-1-[4-(2-furyl)-3-methylphenyl]butane-1,3-dioneHCID 22316748—
SolventEthanolHCID 702—
Product4-[5-[4-(2-Furyl)-3-methylphenyl]-3-(trifluoromethyl)-1H-pyrazol-1-yl]-phenylsulfonamideHCID 2231694920%

Reaction Steps

To a stirred soluition of 4,4,4-trifluoro-1-[4-(2-furyl)-3-methylphenyl]butane-1,3-dione (0.53 g, 1.80 mmol) in ethanol (22.5 ml) was added (4-sulfamoylphenyl)hydrazine hydrochloride (0.44 ml, 1.98 mmol), and the mixture was heated at reflux temperature for 16 hours. The mixture was cooled down to room temperature, and concentrated in vacuo. The residue was dissolved in ethyl acetate. washed with brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by flash chromatography eluting with ethyl acetate/hexane (1/3). The resulting solid was recrystallized with dichloromethane-hexane to give the title compound (0.16 g, 20% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608095B2
Source datasetuspto-grants-2003_08
ORD IDord-67d5e7a112894b58a7b9e1c3daaf64e4
Source noteuspto-grants-2003_08