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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746748Generated: October 30, 2026

Thionyl Chloride → N-(2-Benzoylphenyl)-4-(2-oxopyrrolidin-1-yl)benzene-1-sulfonamide

https://huagongshe.com/reaction/746748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant4-Bromobutyric acidHCID 75809—
Reactant4-Amino-N-(2-benzoylphenyl)benzene-1-sulfonamideHCID 69308994—
SolventHCID 20373099HCID 20373099—
ProductN-(2-Benzoylphenyl)-4-(2-oxopyrrolidin-1-yl)benzene-1-sulfonamideHCID 58664932—

Reaction Steps

A solution of 474 mg (2.84 mmol) of 4-bromo-butanoic acid in 6 mL of 5:1 HMPA/acetonitrile was cooled to 0 deg and thionyl chloride (0.207 mL, 2.84 mmol) was added. The reaction mixture was warmed to room temperature, and transferred to a flask containing 250 mg (0.709 mmol) of neat 4-amino-N-(2-benzoylphenyl)benzenesulfonamide. The solution was allowed to stir overnight. The reaction was quenched w/saturated sodium bicarbonate and diluted with EtOAc (˜100 mL), washed with water (3×20 mL) and brine (1×20 mL), dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified via flash chromatography (15% to 75% EtOAc/hexanes)to provide the title compound. LC/MS (ES MS, M+H+ found: 457).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393873B2
Source datasetuspto-grants-2008_07
ORD IDord-a77776605ad14b689a350caad336b178
Source noteuspto-grants-2008_07