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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851993Generated: October 25, 2026

Potassium Iodide → 4-chloro-N-(4-difluoromethyl-benzyl)-N-(2-oxo-azepan-3-yl)-benzenesulfonamide

https://huagongshe.com/reaction/851993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-N-(2-oxo-azepan-3-yl)-benzenesulfonamideHCID 2738683—
Reactant1-(Bromomethyl)-4-(difluoromethyl)benzeneHCID 57589907—
SolventDimethylformamideHCID 6228—
Product4-chloro-N-(4-difluoromethyl-benzyl)-N-(2-oxo-azepan-3-yl)-benzenesulfonamideHCID 1158307094.8%

Reaction Steps

4-Chloro-N-(2-oxo-azepan-3-yl)-benzenesulfonamide (0.45 g, 1.50 mmol), 1-bromomethyl-4-difluoromethyl-benzene (0.66 g, 3.00 mmol), potassium carbonate (2.09 g, 15.0 mmol) and potassium iodide (0.05 g, 0.20 mmol) in 15 ml dimethylformamide were stirred at 65° C. for 5 hours. Extraction with water/ethylacetate and chromatography on silicagel with ethylacetate/heptane (90/10 to 1/0) yielded 0.63 g (94%) 4-chloro-N-(4-difluoromethyl-benzyl)-N-(2-oxo-azepan-3-yl)-benzenesulfonamide as white solid, MS: m/e (%)=443.0 (MH+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253158B2
Source datasetuspto-grants-2007_08
ORD IDord-96ba3d457c2140679a83886910e6f828
Source noteuspto-grants-2007_08