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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874403Generated: October 30, 2026

Trifluoroacetic anhydride → HCID 57749303, compound

https://huagongshe.com/reaction/1874403

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 68990672HCID 68990672—
SolventDichloromethaneHCID 6344—
ProductHCID 57749303HCID 5774930318.1%

Reaction Steps

A mixture of N-{5-[(1-(2-amino-2-oxoethyl)-6-{[(4-methylphenyl)sulfonyl]amino}-1,6-dihydropyridin-3-yl)oxy]-2-fluorophenyl}-1,3-dimethyl-1H-pyrazole-5-carboxamide (5.85 g, 10.6 mmol), trifluoroacetic anhydride (40 mL) and dichloromethane (40 mL) was stirred at room temperature for 6 hr. The reaction solution was concentrated under reduced pressure, ethyl acetate (50 mL) and saturated aqueous sodium hydrogen carbonate solution (50 mL) were added to the residue and the mixture was stirred for 10 min. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, 8N aqueous sodium hydroxide solution (15 mL) and ethanol (60 mL) were added to the residue. The mixture was stirred at room temperature for 2 hr and at 60° C. for 2 hr. The reaction mixture was diluted with water and extracted with ethyl acetate/tetrahydrofuran (×3). The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was purified by column chromatography (NH silica gel, ethyl acetate) and recrystallized from ethyl acetate-hexane to give the title compound (730 mg, 18%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-4d7d81918c264c7ca9cfc4785050a69a
Source noteuspto-grants-2012_11