Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4'-Fluoroacetophenone | HCID 9828 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(N-Boc-amino)piperidine | HCID 723833 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 57442341 | HCID 57442341 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851474B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-8da94fac617e432f9ff66db9f224c2e3 |
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| Source note | uspto-grants-2010_12 |
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