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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069891Generated: October 25, 2026

Potassium Carbonate → 4-(2-Butynyloxy)-6-(3-trifluoromethylpiperidino)pyrimidine

https://huagongshe.com/reaction/2069891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Butyn-1-olHCID 12991—
Reactant4,6-DifluoropyrimidineHCID 137717—
Reactant3-(Trifluoromethyl)pyrrolidineHCID 5152159—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventTriethylamineHCID 8471—
Product4-(2-Butynyloxy)-6-(3-trifluoromethylpiperidino)pyrimidineHCID 57672951—

Reaction Conditions

Temperature30 °C

Reaction Steps

To a mixture obtained by adding 110.0 g of 4,6-difluoropyrimidine, 132.3 g of potassium carbonate and 19.2 g of triethylamine to 220.0 g of toluene, 69.8 g of 2-butyn-1-ol is added dropwise at 25 to 30° C. over one hour, followed by stirring at 30° C. Then, 220.0 g of water is added dropwise into the reaction mixture, followed by stirring. Then, 152.4 g of 3-trifluoromethylpyrrolidine is added dropwise and, after the mixture is stirred at 30° C., the reaction mixture is allowed to stand. After separating into the organic layer and the aqueous layer, the aqueous layer is removed and the organic layer is washed once with 220.0 g of 5% hydrochloric acid and then washed once with 220.0 g of water. The organic layer is concentrated to obtain 4-(2-butynyloxy)-6-(3-trifluoromethylpiperidino)pyrimidine (hereinafter referred to as the present compound (2)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299245B2
Source datasetuspto-grants-2012_10
ORD IDord-7e674331cfe14eaaafee9cbb79f9b92b
Source noteuspto-grants-2012_10