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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759896Generated: October 31, 2026

Dimethyl Sulfoxide → HCID 22599788, compound

https://huagongshe.com/reaction/1759896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantEthylamineHCID 6341—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(2-Butynyloxy)-6-chloropyrimidineHCID 12137602—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 22599788HCID 22599788—

Reaction Conditions

Temperature50 °C

Reaction Steps

To 20 ml of dimethylsulfoxide were added 1.83 g of 4-chloro-6-(2-butynyloxy)pyrimidine, 2.20 g of potassium carbonate, and 20 ml of ethylamine (2.0 M tetrahydrofuran solution), followed by stirring at 50° C. for 8 hours. The reaction mixture was then left for cooling to room temperature, diluted with tert-butyl methyl ether, and washed twice with an aqueous sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The residue was recrystallized from tert-butyl methyl ether to give 1.14 g of 4-(2-butynyloxy)-6-(ethylamino)pyrimidine (the present compound (108)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06838463B2
Source datasetuspto-grants-2005_01
ORD IDord-d3a3adcfc3cd4ebab866c1cc153c74ad
Source noteuspto-grants-2005_01