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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606236Generated: October 29, 2026

Sodium Bicarbonate → 1-(1-(3-Tert-butoxy-2-quinoxalinylmethyl)piperidin-4-yl]-2-(2-methylphenyl)ethanone

https://huagongshe.com/reaction/606236

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant2-Tert-butoxyquinoxaline-3-carboxaldehydeHCID 22248239—
Reactant2-(2-Methylphenyl)-1-(piperidin-4-yl)ethanone hydrochlorideHCID 22248475—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product1-(1-(3-Tert-butoxy-2-quinoxalinylmethyl)piperidin-4-yl]-2-(2-methylphenyl)ethanoneHCID 2224810563%

Reaction Steps

After suspending 183 mg of 2-(2-methylphenyl)-1-(piperidin-4-yl)ethanone hydrochloride in 3 ml of dichloromethane, 150 mg of 2-tert-butoxyquinoxaline-3-carboxaldehyde and 180 mg of sodium triacetoxyborohydride were added while stirring, and the stirring was continued overnight at room temperature. Aqueous sodium bicarbonate solution was added to the reaction mixture and extraction was performed with ethyl acetate. The organic layer was washed with water and saturated brine in that order and dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (solvent: n-hexane/ethyl acetate) to obtain 1-[1-(3-tert-butoxy-2-quinoxalinylmethyl)piperidin-4-yl]-2-(2-methylphenyl)ethanone (177 mg, 63% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915274B2
Source datasetuspto-grants-2011_03
ORD IDord-058b42244839416b9e13c98203855d5a
Source noteuspto-grants-2011_03