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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268131Generated: October 27, 2026

Thionyl Chloride → 4-Phenylethynyl-N-(2-sulfamoylphenyl)benzamide

https://huagongshe.com/reaction/1268131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-AminobenzenesulfonamideHCID 72894—
Reactant4-(2-Phenylethynyl)benzoic acidHCID 4308903—
SolventBenzeneHCID 241—
Product4-Phenylethynyl-N-(2-sulfamoylphenyl)benzamideHCID 1204304378.7%

Reaction Steps

A benzene (30 ml) solution containing 3.00 g (13.5 mmol) of 4-phenylethynylbenzoic acid and 2 ml of thionyl chloride was heated under reflux for 2 hours and then the solvent was evaporated under a reduced pressure. The resulting residue was dissolved in methylene chloride (30 ml), this solution was added dropwise under ice-cooling to a pyridine (50 ml) solution containing 2.32 g (13.50 mmol) of 2-aminobenzenesulfonamide, the mixture was stirred at room temperature for 18 hours and then methylene chloride was evaporated under a reduced pressure. The resulting residue was dissolved in ethyl acetate, washed with a 1 N hydrochloric acid aqueous solution, water and saturated brine in that order and dried over anhydrous sodium sulfate, and then the solvent was evaporated under a reduced pressure. The resulting residue was recrystallized from ethyl acetate-hexane to obtain 4.00 g (yield: 78.7%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555584B1
Source datasetuspto-grants-2003_04
ORD IDord-205b1f2b980f44a08d01773032056356
Source noteuspto-grants-2003_04