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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710604Generated: October 26, 2026

4-(Difluoromethoxy)benzenesulfonyl chloride → 4-Difluoromethoxy-N-[4-methoxy-3-(4-methyl-piperazin-1-yl)-phenyl]-benzenesulfonamide

https://huagongshe.com/reaction/1710604

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Difluoromethoxy)benzenesulfonyl chlorideHCID 2778223—
Reactant4-Methoxy-3-(4-methylpiperazin-1-yl)anilineHCID 10331101—
SolventPyridineHCID 1049—
Product4-Difluoromethoxy-N-[4-methoxy-3-(4-methyl-piperazin-1-yl)-phenyl]-benzenesulfonamideHCID 4260283481.8%

Reaction Steps

0.18 mL of 4-difluoromethoxybenzene sulfonyl chloride (1.13 mmol) were added to a solution of 0.25 g of (1.13 mmol) 4-methoxy-3-(4-methyl-piperazin-1-yl)-phenylamine in 10 mL of pyridine. The reaction mixture was stirred for 16 h at room temperature. The solvent was evaporated at reduced pressure. After addition of toluene and dichloromethane the mixture was again evaporated twice. The thus obtained residue was partitioned between dichloromethane and 5% aqueous ammoniumchloride. The organic phase was washed with saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered, and the solvent was evaporated under reduced pressure. The obtained crude product was further purified via HPLC to yield 0.395 g of the desired title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790727B2
Source datasetuspto-grants-2010_09
ORD IDord-7741a19bab1b4660b445be4d6848dd4f
Source noteuspto-grants-2010_09