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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759900Generated: October 28, 2026

Dimethyl Sulfoxide → HCID 22599716, compound

https://huagongshe.com/reaction/1759900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantPotassium CarbonateHCID 11430—
Reactant2,2,3,3,3-PentafluoropropylamineHCID 79002—
Reactant4-(2-Butynyloxy)-6-chloropyrimidineHCID 12137602—
SolventEthyl AcetateHCID 8857—
ProductHCID 22599716HCID 2259971612.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To 4 ml of dimethylsulfoxide were added 365 mg of 4-chloro-6-(2-butynyloxy)pyrimidine, 442 mg of potassium carbonate, and 495 mg of 2,2,3,3,3-pentafluoropropylamine, followed by stirring at 80° C. for 4 hours. Then, 596 mg of 2,2,3,3,3-pentafluoropropylamine was further added, and the mixture was stirred at 100° C. for 6 hours. The reaction mixture was then left for cooling to room temperature, diluted with ethyl acetate, and washed twice with an aqueous sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography to give 73 mg of 4-(2-butynyloxy)-6-(2,2,3,3,3-pentafluoropropylamino)pyrimidine (the present compound (111)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06838463B2
Source datasetuspto-grants-2005_01
ORD IDord-4ed581aa5845465f9ebafaab19111087
Source noteuspto-grants-2005_01