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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45885Generated: October 26, 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/45885

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 numberUS08541575B2
Source datasetuspto-grants-2013_09
ORD IDord-4bb388d729bb4bc290abe61675222a08
Source noteuspto-grants-2013_09