Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843666Generated: October 29, 2026

2,5-Difluorobenzenesulfonyl chloride → N-{3-[4-(2-aminopyrimidin-4-yl)-1-(4-methoxybenzyl)-1H-pyrazol-3-yl]phenyl}-2,5-difluorobenzenesulfonamide

https://huagongshe.com/reaction/1843666

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Difluorobenzenesulfonyl chlorideHCID 2736911—
ReactantSodiumHCID 5360545—
Reactant4-[3-(3-aminophenyl)-1-(4-methoxybenzyl)-1H-pyrazol-4-yl]pyrimidin-2-amineHCID 67184185—
SolventPyridineHCID 1049—
ProductN-{3-[4-(2-aminopyrimidin-4-yl)-1-(4-methoxybenzyl)-1H-pyrazol-3-yl]phenyl}-2,5-difluorobenzenesulfonamideHCID 6718434731%

Reaction Steps

175 mg (0.47 mmol) of 4-[3-(3-aminophenyl)-1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-pyrimidin-2-amine were dissolved with 10 ml of dry pyridine and 63 μl of 2,5-difluorobenzensulfonylchloride were added under stirring. The solution was maintained at room temperature overnight. The reaction mixture was then poured into aqueous sodium hydrogenocarbonate and extracted with dichloromethane. The organic layer was dried over sodium sulphate and evaporated to dryness. The residue was purified by flash-chromatography on a silica gel column (CH2Cl2-CH3COCH3; from 9/1 to 8/2), giving 80 mg (31%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946250B2
Source datasetuspto-grants-2015_02
ORD IDord-1dd4ff1adbb54e81956a336cdab3f061
Source noteuspto-grants-2015_02