Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776983Generated: October 31, 2026

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

https://huagongshe.com/reaction/1776983

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 numberUS09266830B2
Source datasetuspto-grants-2016_02
ORD IDord-9f7e7da1ca9b4389b5739be2fb26877b
Source noteuspto-grants-2016_02