HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl 4-((S)-3-(benzyloxycarbonylamino)-2-oxopyrrolidin-1-yl)-3,3-dimethylpiperidine-1-carboxylate → tert-butyl 4-((S)-3-amino-2-oxopyrrolidin-1-yl)-3,3-dimethylpiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl 4-((S)-3-(benzyloxycarbonylamino)-2-oxopyrrolidin-1-yl)-3,3-dimethylpiperidine-1-carboxylate | HCID 67469782 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-butyl 4-((S)-3-amino-2-oxopyrrolidin-1-yl)-3,3-dimethylpiperidine-1-carboxylate | HCID 67469742 | 105.6% |
Reaction Steps
tert-Butyl 4-((S)-3-(benzyloxycarbonylamino)-2-oxopyrrolidin-1-yl)-3,3-dimethylpiperidine-1-carboxylate (0.81 g, 1.8 mmol) was dissolved in methanol (20 mL) and the mixture was purged with N2 by three vacuum pump/N2 balloon cycles. 10% Palladium on carbon (dry basis, wet, Degussa type, 0.5 g) was added and the system was purged with 1 atm H2 by three vacuum pump/H2 balloon cycles. The reaction was stirred under the H2 atmosphere until the starting material was consumed. The mixture was filtered through Celite® and concentrated to afford tert-butyl 4-((S)-3-amino-2-oxopyrrolidin-1-yl)-3,3-dimethylpiperidine-1-carboxylate (0.59 g, 1.9 mmol, 100% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754226B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-b9996ab053364a1abe2f9733185c8d19 |
| Source note | uspto-grants-2014_06 |