Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Piperidinamine | HCID 424361 | — |
| Reactant | Tert-butyl 4-fluorobenzoate | HCID 2736444 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 22557720 | HCID 22557720 | — |
Reaction Steps
4-fluorobenzoic acid tert-butyl ester (19.6 g, 100 mmol) was dissolved in dimethyl sulfoxide (hereinafter referred to as DMSO) (50 ml), and potassium carbonate (20.7 g, 150 mmol) and 4-aminopiperidine (11.0 g, 110 mmol) were added thereto, followed by stirring at 120° C. for 17 hours. After the reaction mixture was cooled to room temperature, water was added to the mixture, and the precipitate was collected by filtration, thereby obtaining 4-(4-aminopiperidin-1-yl)-benzoic acid tert-butyl ester (23.3 g, 84%) as a milky-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765750B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-cd7894c7a6794d0d835866f26849e634 |
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| Source note | uspto-grants-2014_07 |
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