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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699437Generated: October 25, 2026

Potassium Carbonate → 2-(4-[4-(4,5-Dichloro-2-methylimidazol-1-yl)butyl]piperazin-1-yl}-5-fluoropyrimidine

https://huagongshe.com/reaction/1699437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Fluoro-2-(piperazin-1-yl)pyrimidineHCID 10058158—
Reactant1-(4-chlorobutyl)-4,5-dichloro-2-methyl-1H-imidazoleHCID 18320553—
SolventDimethylformamideHCID 6228—
Product2-(4-[4-(4,5-Dichloro-2-methylimidazol-1-yl)butyl]piperazin-1-yl}-5-fluoropyrimidineHCID 980834283%

Reaction Steps

A mixture of 3.5 g (0.02 mol) of 5-fluoro-2-(piperazin-1-yl)pyrimidine, 6.04 g (0.025 mol) of 1-(4-chlorobutyl)-4,5-dichloro-2-methyl-1H-imidazole and 4.14 g (0.03 mol) of potassium carbonate in 200 ml of dimethylformamide is maintained at reflux for 12 hours. The mixture is subsequently evaporated to dryness and the resulting crude product is redissolved in chloroform and washed repeatedly with water. The organic phase is dried and evaporated, and then the resulting crude product is purified by chromatography on a columm of silica gel. 6.4 g (83% yield) of 2-{4-[4-(4,5-dichloro-2-methylimidazol-1-yl)butyl]piperazin-1-yl}-5-fluoropyrimidine are obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06346620B1
Source datasetuspto-grants-2002_02
ORD IDord-a0d8b790fab84f468c5660216a655c65
Source noteuspto-grants-2002_02