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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851994Generated: October 25, 2026

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

https://huagongshe.com/reaction/851994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Bromomethyl)benzonitrileHCID 86996—
Reactant4-Chloro-N-(2-oxo-azepan-3-yl)-benzenesulfonamideHCID 2738683—
SolventDimethylformamideHCID 6228—
Product4-chloro-N-(4-cyano-benzyl)-N-(2-oxo-azepan-3-yl)-benzenesulfonamideHCID 1845514363%

Reaction Steps

4-Chloro-N-(2-oxo-azepan-3-yl)-benzenesulfonamide (1.21 g, 4.00 mmol), 4-(bromomethyl)-benzonitrile (0.79 g, 4.00 mmol), potassium carbonate (5.58 g, 40.0 mmol) and potassium iodide (0.13 g, 0.80 mmol) in 200 ml dimethylformamide were stirred at 65° C. for 16 hours. Extraction with water/ethylacetate and chromatography on silicagel with ethylacetate yielded 1.05 g (63%) 4-chloro-N-(4-cyano-benzyl)-N-(2-oxo-azepan-3-yl)-benzenesulfonamide as white solid, MS: m/e (%)=418.1 (MH+, 100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253158B2
Source datasetuspto-grants-2007_08
ORD IDord-0d574b37941247e19c198a37aff3e2c9
Source noteuspto-grants-2007_08