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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2288744Generated: November 1, 2026

Triethylamine → 1-(4-Cyanobenzoyl)-4-[1-(4-pyrimidinyl)piperidin-4-ylcarbonyl] piperazine

https://huagongshe.com/reaction/2288744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Cyanobenzoyl chlorideHCID 80172—
Reactant1-[1-(4-Pyrimidinyl)-4-piperidylcarbonyl]piperazineHCID 18697970—
SolventDichloromethaneHCID 6344—
Product1-(4-Cyanobenzoyl)-4-[1-(4-pyrimidinyl)piperidin-4-ylcarbonyl] piperazineHCID 1869805646.2%

Reaction Steps

A solution of 4-cyanobenzoyl chloride (298 mg) in methylene chloride (10 ml) was added to a stirred mixture of 1-[1(4-pyrimidinyl) piperidin-4-ylcarbonyl]piperazine (412.5 mg) and triethylamine (0.28 ml) in methylene chloride (15 ml) and the resultant mixture was stirred at ambient temperature for 2 hours. The mixture was partitioned between methylene chloride and water. The organic phase was washed with water, dried (Na2SO4) and evaporated. The residue was purified by column chromatography using 0.5% methanol in methylene chloride. Recrystallisation from ethyl acetate/hexane gave, as a solid 1-(4-cyanobenzoyl)-4-[1-(4-pyrimidinyl)piperidin-4-ylcarbonyl] piperazine (280 mg): mpt 192-193° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06090813
Source datasetuspto-grants-2000_07
ORD IDord-038e4a9a567d41dabd787e6020cf9e75
Source noteuspto-grants-2000_07