Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | p-Fluorophenyl 4-piperidyl ketone hydrochloride | HCID 3084438 | — |
| Reactant | tert-butyl N-(4-bromobutyl)carbamate | HCID 10868765 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66628219 | HCID 66628219 | 100% |
Reaction Steps
4-(4-fluorobenzoyl)piperidine hydrochloride (0.5 g, 2.01 mmol) is suspended in acetonitrile (5 mL), 4-(Boc-amino) Butyl Bromide was added (0.569 g, 2.01 mmol) and sodium iodide (0.461 g, 3.02 mmol) and the mixture was stirred at 80° C. overnight. Water was added and the aqueous phase was extracted with 30 mL dichloromethane. The combined organic phases were dried with magnesium sulfate, filtrated concentrated and purified with column chromatography on silica using dichloromethane/Methanol (95/0.5) to yield 0.830 g, (2.1 mmol, 100% yield) of the title compound as a brown solid. MS (m/e): 379.2 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415350B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-20a0be04ebec4dc3b790c4c452acecbc |
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| Source note | uspto-grants-2013_04 |
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