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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843672Generated: October 28, 2026

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

https://huagongshe.com/reaction/1843672

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Difluorobenzenesulfonyl chlorideHCID 2736911—
ReactantSodiumHCID 5360545—
Reactant4-[3-(3-aminophenyl)-1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-N-ethylpyrimidin-2-amineHCID 67184831—
SolventPyridineHCID 1049—
ProductN-(3-{4-[2-(ethylamino)pyrimidin-4-yl]-1-(4-methoxybenzyl)-1H-pyrazol-3-yl}phenyl)-2,5-difluorobenzenesulfonamideHCID 6718503791.8%

Reaction Steps

340 mg (0.85 mmol) of 4-[3-(3-aminophenyl)-1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-N-ethylpyrimidin-2-amine were dissolved in 10 ml of dry pyridine and 114 μl (0.85 mmol) of 2,5-difluorobenzensulfonyl chloride were added. The resulting solution was stirred at room temperature overnight. The mixture was then poured into aqueous sodium hydrogenocarbonate and extracted with dichloromethane. The organic layer was finally dried over sodium sulphate and evaporated, giving 450 mg (91%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946250B2
Source datasetuspto-grants-2015_02
ORD IDord-3f073333aa6e4406823f33d7c1579120
Source noteuspto-grants-2015_02