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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262717Generated: November 4, 2026

Water → HCID 57442341, compound

https://huagongshe.com/reaction/2262717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4'-FluoroacetophenoneHCID 9828—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 57442341HCID 57442341—

Reaction Conditions

Temperature90 °C

Reaction Steps

To a solution of piperidin-4-yl-carbamic acid tert-butyl ester (24 mmol) in anhydrous DMSO (20 mL) is added 1-(4-fluoro-phenyl)-ethanone (24 mmol) and potassium carbonate (24 mmol). The resulting mixture is heated at 90° C. for 36 hr. The reaction mixture is allowed to cool to rt, poured into cold water (100 mL), and extracted with EtOAc (40 mL×3). The combined organic layers are washed with water and brine, dried over sodium sulfate, and concentrated. The crude product is purified through silica gel flash chromatography (hexane/ethyl acetate 2:1) to give [1-(4-acetyl-phenyl)-piperidin-4-yl]-carbamic acid tert-butyl ester, which is refluxed in HCl—MeOH solution. Removing MeOH in vacuo gives the hydrochloride salt of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851474B2
Source datasetuspto-grants-2010_12
ORD IDord-8da94fac617e432f9ff66db9f224c2e3
Source noteuspto-grants-2010_12