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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49781Generated: October 27, 2026

4-Fluorobenzenesulfonyl chloride → N-(1-acetylpiperidin-4-yl)-4-fluorobenzenesulfonamide

https://huagongshe.com/reaction/49781

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Acetyl-4-aminopiperidine hydrochlorideHCID 17221642—
SolventDichloromethaneHCID 6344—
ProductN-(1-acetylpiperidin-4-yl)-4-fluorobenzenesulfonamideHCID 992635067,058.898%

Reaction Steps

To a suspension of 1-acetyl-4-aminopiperidine hydrochloride (715 mg) in dichloromethane (7 ml) were added diisopropylethylamine (1.83 ml) and a solution of 4-fluorobenzenesulfonyl chloride (0.83 mg) in dichloromethane (2 ml) at ambient temperature. After stirring for 6.5 hours, the reaction mixture was diluted with dichloromethane and washed with water, saturated aqueous sodium hydrogen carbonate, and brine. After drying with magnesium sulfate, the solvents were removed under reduced pressure. A residue was purified by column chromatography (silica gel 50 ml, dichloromethane:methanol=50:1 to 20:1). After rinse with diisopropyl ether, N-(1-acetylpiperidin-4-yl)-4-fluorobenzenesulfonamide (859 mg) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710043B1
Source datasetuspto-grants-2004_03
ORD IDord-9cbd0361abc743968418ad4fd839c0eb
Source noteuspto-grants-2004_03