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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621507Generated: October 25, 2026

Potassium Carbonate → HCID 14074112, compound

https://huagongshe.com/reaction/621507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chloro-5,6-dimethyl-2-phenylpyrimidineHCID 13487935—
ReactantHCID 21243172HCID 21243172—
SolventDimethylformamideHCID 6228—
ProductHCID 14074112HCID 1407411276%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 4.42 g (12 mmol) of 1-(4-hydroxy-3,5-dimethylphenyl)piperazine dihydrobromide, 2.84 g (13 mmole) of 4-chloro-5,6-dimethyl-2-phenylpyrimidine, 1.66 g (12 mmol) of powdered K2CO3 and 38 ml of absolute DMF was warmed to 90° C., and 277 mg of powdered K2CO3 were added at 90° C. with stirring in each case after 10 minutes, after a further 25 minutes and after a further 60 minutes (in total 6 mmol of K2CO3), and the mixture was stirred for a further 6 hours at 95° C. The DMF was subsequently removed by distillation in vacuo, the residue was taken up in CH2Cl2 /water, the phases were separated after through mixing, and the aqueous phase was extracted a further three times with CH2Cl2. The combined CH2Cl2 extracts were dried, filtered and evaporated in vacuo. The crystalline residue (5.2 g) was boiled with 15 ml of methanol, and the crystals were filtered off under suction after cooling in an ice bath. In this fashion, 3.54 g (=76% yield) of pure 1-(4-hydroxy-3,5-dimethylphenyl)-4-(5,6-dimethyl-2-phenylpyrimidin-4-yl)piperazine, melting point 188°-89° C., were obtained;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04824846
Source datasetuspto-grants-1989_04
ORD IDord-2b69ccacd08f43c0bb9777b8c45a0948
Source noteuspto-grants-1989_04