Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | HCID 15289252 | HCID 15289252 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86694324 | HCID 86694324 | 99.7% |
Reaction Steps
Under a nitrogen atmosphere, to a solution of 1.5 g of tert-butyl 4-[3-(pyridin-3-yl)propanoyl]piperazine-1-carboxylate in 25 mL of tetrahydrofuran was added 7 mL of a 1 M borane/tetrahydrofuran solution under ice-cooling. The mixture was heated to reflux for 6 hours, and then cooled to room temperature, and 10 mL of methanol was added thereto, followed by further heating to reflux for 16 hours. After cooling to room temperature, the mixture was concentrated under reduced pressure, and a mixture of a saturated aqueous sodium hydrogen carbonate solution and ethyl acetate was added thereto. The aqueous layer was separated, and then the organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (chloroform/methanol) to obtain 1.43 g of tert-butyl 4-[3-(pyridin-3-yl)propyl]piperazine-1-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822448B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-2da19d95010a42a18b7dd1c4d4a5406b |
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| Source note | uspto-grants-2014_09 |
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