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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289522Generated: November 2, 2026

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

https://huagongshe.com/reaction/2289522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Cyanobenzenesulfonyl chlorideHCID 39497—
Reactant1-[1-(4-Pyrimidinyl)-4-piperidylcarbonyl]piperazineHCID 18697970—
SolventDichloromethaneHCID 6344—
Product1-(4-Cyanobenzenesulphonyl)-4-[1-(4-pyrimidinyl)piperidin-4-ylcarbonyl]piperazineHCID 1869806142.4%

Reaction Steps

A solution of 4-cyanophenylsulphonyl chloride (363 mg) in dichloromethane (10 ml) was added to a stirred mixture of 1-[1-(4-pyrimidinyl)-4-piperidylcarbonyl] piperazine (412.5 mg) and triethylamine (0.28 ml) in dichloromethane (15 ml) and the resultant mixture was stirred at ambient temperature for 2 hours. The mixture was partitioned between dichloromethane and water, and the organic phase washed with water, dried (Na2SO4) and evaporated. The residue was purified by column chromatography using 0.5% methanol in dichloromethane. Recrystallisation from ethyl acetate/hexane gave, as a solid 1-(4-cyanophenylsulphonyl)-4-[1-(4-pyrimidinyl)-4-piperidylcarbonyl] piperazine (280 mg), mp 180-181° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093718
Source datasetuspto-grants-2000_07
ORD IDord-a540351563c94ff09946ce42eb03d349
Source noteuspto-grants-2000_07