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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356954Generated: November 3, 2026

Dimethylformamide → 3-[3-(Azetidin-3-ylamino)-4-(trifluoromethoxy)phenyl]-5,5-dimethyl-1-(pyridin-4-ylmethyl)imidazolidine-2,4-dione;2,2,2-trifluoroacetic acid

https://huagongshe.com/reaction/2356954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium formateHCID 2723923—
Reactant3-(3-Amino-4-trifluoromethoxyphenyl)5,5-dimethyl-1-pyridin-4-ylmethylimidazolidine-2,4-dioneHCID 23110308—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-[3-(Azetidin-3-ylamino)-4-(trifluoromethoxy)phenyl]-5,5-dimethyl-1-(pyridin-4-ylmethyl)imidazolidine-2,4-dione;2,2,2-trifluoroacetic acidHCID 86617225—

Reaction Conditions

Temperature80 °C

Reaction Steps

394 mg (1 mmol) of 3-(3-amino-4-trifluoromethoxyphenyl)-5,5-dimethyl-1-pyridin-4-ylmethylimidazolidine-2,4-dione were dissolved in 1 ml of DMF, 166 mg (1.2 mmol) of potassium carbonate and 413 mg (1.3 mmol) of 1-(diphenylmethyl)-3-azetidine methanesulphonate were added, and the mixture was stirred at 80° C. for 5 h. For workup, the mixture was added to ice-water, extracted with CH2C12, dried and concentrated. The remaining residue was purified by means of preparative HPLC (RP18, acetonitrile/water, 0.1% TFA). The intermediate obtained in this way was dissolved in 3 ml of methanol, admixed with 10 mg of 5% Pd/C and 50 mg (0.8 mmol) of ammonium formate, and heated under reflux for 2 h. The residue remaining after filtration and evaporation 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-a43a9470e0844dce9252d0a8ad53c660
Source noteuspto-grants-2010_07