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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699436Generated: 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/1699436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4,5-Dichloro-2-methyl-1H-imidazoleHCID 312390—
Reactant8-(5-Fluoro-2-pyrimidinyl)-8-aza-5-azoniaspiro[4.5]decaneHCID 12044789—
SolventDimethylformamideHCID 6228—
Product2-(4-[4-(4,5-Dichloro-2-methylimidazol-1-yl)butyl]piperazin-1-yl}-5-fluoropyrimidineHCID 980834285.2%

Reaction Steps

A mixture of 3.17 g (0.01 mol) of 8-(5-fluoro-2-pyrimidinyl)-8-aza-5-azoniaspiro[4.5]decane, 2.26 g (0.015 mol) of 4,5-dichloro-2-methyl-1H-imidazole and 76 g (0.02 mol) of potassium carbonate in 80 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 column of silica gel. 3.3 g (85% 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-27078bcc6fc3413fa4bc9d9150cb1a8b
Source noteuspto-grants-2002_02