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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890105Generated: October 29, 2026

Sodium Bicarbonate → 3-[4-Hydroxy-4-[(2-fluorophenyl)ethynyl)piperidino]methyl-1H-pyridin-2-one

https://huagongshe.com/reaction/890105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Oxo-1,2-dihydropyridine-3-carbaldehydeHCID 7062196—
Reactant4-Hydroxy-4-[(2-fluorophenyl)ethynyl]piperidine hydrochlorideHCID 22248440—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product3-[4-Hydroxy-4-[(2-fluorophenyl)ethynyl)piperidino]methyl-1H-pyridin-2-oneHCID 2224843510%

Reaction Steps

After then adding 253 mg of the 4-hydroxy-4-[(2-fluorophenyl)ethynyl]piperidine hydrochloride to 10 ml of dichloromethane, 158 mg of 2-oxo-1,2-dihydropyridine-3-carboxaldehyde was added and the mixture was stirred for 10 minutes at room temperature. Next, 315 mg of sodium triacetoxyborohydride was added and the mixture was stirred overnight at room temperature. Saturated aqueous sodium bicarbonate solution was added to the reaction mixture and extraction was performed with ethyl acetate. After drying the organic layer over magnesium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by NH silica gel column chromatography to obtain the title compound (32 mg, 10% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06995144B2
Source datasetuspto-grants-2006_02
ORD IDord-8f491786983e41c1a371fba2c8e6541b
Source noteuspto-grants-2006_02