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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41315Generated: October 25, 2026

Ethyl Acetate → (2R)-4-[(4-chlorophenyl)sulfonyl]-2-methyl-1-(2-pyridinylcarbonyl)piperazine

https://huagongshe.com/reaction/41315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantPyridine-2-carbonyl chlorideHCID 135034—
Reactant(3R)-1-[(4-chlorophenyl)sulfonyl]-3-methylpiperazineHCID 11630465—
SolventAcetonitrileHCID 6342—
Product(2R)-4-[(4-chlorophenyl)sulfonyl]-2-methyl-1-(2-pyridinylcarbonyl)piperazineHCID 4461208345.5%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of (3R)-1-[(4-chlorophenyl)sulfonyl]-3-methylpiperazine (0.15 g, 0.55 mmol) in dry acetonitrile (5 mL) was added potassium carbonate (90 mg, 0.66 mmol) and 2-pyridinecarbonyl chloride (106 mg, 0.60 mmol) and the reaction mixture heated at 85° C. for 24 h. To the mixture was added ethyl acetate (30 mL) and the organic phase washed with 10% aqueous sodium bicarbonate (50 mL) before it was dried (MgSO4), filtered and the solvent evaporated. The crude product was purified by Biotage SP4 (12+M silica column) eluting 0-4% MeOH in DCM to give the title compound as an off-white solid (95 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530478B2
Source datasetuspto-grants-2013_09
ORD IDord-626bff4e6de04ebe8ef8b3da38d7a452
Source noteuspto-grants-2013_09