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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356955Generated: October 31, 2026

Trifluoroacetic anhydride → N-[5-[4,4-dimethyl-2,5-dioxo-3-(pyridin-4-ylmethyl)imidazolidin-1-yl]-2-(trifluoromethoxy)phenyl]-2,2,2-trifluoroacetamide;2,2,2-trifluoroacetic acid

https://huagongshe.com/reaction/2356955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
Reactant3-(3-Amino-4-trifluoromethoxyphenyl)5,5-dimethyl-1-pyridin-4-ylmethylimidazolidine-2,4-dioneHCID 23110308—
SolventPyridine methylene chlorideHCID 21875418—
ProductN-[5-[4,4-dimethyl-2,5-dioxo-3-(pyridin-4-ylmethyl)imidazolidin-1-yl]-2-(trifluoromethoxy)phenyl]-2,2,2-trifluoroacetamide;2,2,2-trifluoroacetic acidHCID 131728248—

Reaction Conditions

Temperature0 °C

Reaction Steps

394 mg (1.0 mmol) of 3-(3-amino-4-trifluoromethoxyphenyl)-5,5-dimethyl-1-pyridin-4-ylmethylimidazolidine-2,4-dione were dissolved in 5 ml of 4:1 dichloromethane/pyridine and cooled to 0° C., and 252 mg (1.2 mmol) of trifluoroacetic anhydride dissolved in 5 ml of 4:1 dichloromethane/pyridine were added dropwise at 0° C. After stirring at RT, the mixture was added to ice-water, extracted with CH2Cl2, concentrated and dried. The remaining residue was purified by means of preparative HPLC (RP18, acetonitrile/water, 0.1% TFA).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759379B2
Source datasetuspto-grants-2010_07
ORD IDord-606b22cbcd2c429388da196473a99e98
Source noteuspto-grants-2010_07