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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14547Generated: October 28, 2026

Potassium Carbonate → 4-(2-Butynyloxy)-5-fluoro-6-(3,3,5,5-tetramethylpiperidino)pyrimidine

https://huagongshe.com/reaction/14547

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(2-Butynyloxy)-5-fluoro-6-chloropyrimidineHCID 22599717—
ReactantHCID 66594924HCID 66594924—
SolventAcetonitrileHCID 6342—
Product4-(2-Butynyloxy)-5-fluoro-6-(3,3,5,5-tetramethylpiperidino)pyrimidineHCID 5781981472.3%

Reaction Conditions

Temperature70 °C

Reaction Steps

Into 2 ml of acetonitrile were added 0.20 g of 4-(2-butynyloxy)-6-chloro-5-fluoropyrimidine, 0.54 g of potassium carbonate and 0.30 g of 3,3,5,5-tetramethylpiperidine hydrochloride, and the mixture was stirred for 4 hours at 70° C. The reaction mixture was cooled to near room temperature, a saturated ammonium chloride aqueous solution was added therein, and the mixture was extracted with tert-butyl methyl ether three times. The organic layers were washed with a saturated sodium chloride aqueous solution, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.22 g of 4-(2-butynyloxy)-5-fluoro-6-(3,3,5,5-tetramethylpiperidino)pyrimidine (hereinafter, referred to as Compound (39)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732448B2
Source datasetuspto-grants-2010_06
ORD IDord-a0589c26f80e414f859dfb1aadbba84b
Source noteuspto-grants-2010_06