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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098316Generated: November 3, 2026

Potassium Carbonate → Ethyl 2-[3-(3,4,5-trichlorophenyl)-3-(trifluoromethyl)-pyrrolidin-1-yl]-4-(trifluoromethyl)pyrimidine-5-carboxylate

https://huagongshe.com/reaction/2098316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 2-chloro-4-(trifluoromethyl)pyrimidine-5-carboxylateHCID 2780355—
Reactant3-(3,4,5-Trichlorophenyl)-3-(trifluoromethyl)pyrrolidineHCID 59453372—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-[3-(3,4,5-trichlorophenyl)-3-(trifluoromethyl)-pyrrolidin-1-yl]-4-(trifluoromethyl)pyrimidine-5-carboxylateHCID 5945335895%

Reaction Conditions

Temperature100 °C

Reaction Steps

Ethyl 2-chloro-4-(trifluoromethyl)pyrimidine-5-carboxylate (1.2 g) [see J. Med. Chem., 43, 3995 (2000)], 3-(3,4,5-trichlorophenyl)-3-(trifluoromethyl)pyrrolidine (1.5 g), and potassium carbonate (0.7 g) were added to N,N-dimethylformamide (50 mL) and the mixture was heated at 100° C. for 5 hours. After cooling, the reaction solution was poured over ice water, and then extracted with ethyl acetate. The organic layer was dried over magnesium sulfate. The solvent was evaporated off under reduced pressure, and the residue was then purified by a silica gel chromatography to obtain the title compound (2.4 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450483B2
Source datasetuspto-grants-2013_05
ORD IDord-cb0c3156a01d4f7b9c62be1ec2755337
Source noteuspto-grants-2013_05