Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730239Generated: October 28, 2026

4-Chlorobenzenesulfonyl chloride → 5-bromo-N-[2-(4-chlorobenzenesulfonylamino)-4-fluorophenyl]-2-methoxybenzenesulfonamide

https://huagongshe.com/reaction/730239

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
Reactant5-bromo-N-(4-fluoro-2-aminophenyl)-2-methoxybenzenesulfonamideHCID 68948886—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product5-bromo-N-[2-(4-chlorobenzenesulfonylamino)-4-fluorophenyl]-2-methoxybenzenesulfonamideHCID 1159923078.2%

Reaction Steps

To a solution of 5-bromo-N-(4-fluoro-2-aminophenyl)-2-methoxybenzenesulfonamide (0.1 mmol) in pyridine (0.5 mL) and DCM (2 mL), 4-chlorobenzenesulfonyl chloride (0.12 mmol) was added. The reaction mixture was stirred at room temperature for 4 h and then diluted with ethyl acetate (10 mL). The contents were washed with 10% aqueous HCl (10 mL) and brine (10 mL), dried over sodium sulfate, and concentrated under vacuum. The residue obtained was purified by column chromatography eluting with hexanes/ethyl acetate (1:1) followed by ethyl acetate to give 43 mg of 5-bromo-N-[2-(4-chlorobenzenesulfonylamino) -4-fluorophenyl]-2-methoxybenzenesulfonamide. LC: Tr 1.10 min, MS: 551.8 (M+1)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582673B2
Source datasetuspto-grants-2009_09
ORD IDord-d8c9d71a0ef041cba4c306be9a74da85
Source noteuspto-grants-2009_09