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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1631546Generated: November 1, 2026

Diethyl Ether → N-[(2,5-difluorophenyl)sulfonyl]-N-{3-[1-ethyl-4-(pyridin-4-yl)-1H-pyrazol-3-yl]-2,4-difluorophenyl}acetamide

https://huagongshe.com/reaction/1631546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAcetyl chlorideHCID 6367—
ReactantN-{2,4-difluoro-3-[1-ethyl-4-(pyridin-4-yl)-1H-pyrazol-3-yl]phenyl}-2,5-difluorobenzenesulfonamideHCID 44622209—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-[(2,5-difluorophenyl)sulfonyl]-N-{3-[1-ethyl-4-(pyridin-4-yl)-1H-pyrazol-3-yl]-2,4-difluorophenyl}acetamideHCID 5334126291%

Reaction Steps

N-{2,4-difluoro-3-[1-ethyl-4-(pyridin-4-yl)-1H-pyrazol-3-yl]phenyl}-2,5-difluorobenzenesulfonamide (80 mg, 0.168 mmol) was suspended in 3.5 mL of DCM and TEA (18.7 mg, 25.8 μL, 0.185 mmol) was added. Acetyl chloride (20.0 mg, 18.0 μL, 0.252 mmol) was added to the solution so obtained, and the reaction mixture was stirred at room temperature overnight, diluted with DCM, and poured in water. The organic layer was washed three times with water, once with brine, dried over Na2SO4 and concentrated to dryness. The solid so obtained was taken up with ethyl ether and filtered (79 mg, 91% yield)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791265B2
Source datasetuspto-grants-2014_07
ORD IDord-3b964343fa184b3a8e9be5902dfbd1ec
Source noteuspto-grants-2014_07