HuagongsheHuagongshe Chemistry Print Report · For research reference only
(S)-benzyl 4-(3-(tert-butoxycarbonylamino)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate → (S)-tert-butyl 2-oxo-1-(piperidin-4-yl)pyrrolidin-3-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (S)-benzyl 4-(3-(tert-butoxycarbonylamino)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate | HCID 86688075 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (S)-tert-butyl 2-oxo-1-(piperidin-4-yl)pyrrolidin-3-ylcarbamate | HCID 86688117 | 83% |
Reaction Steps
To a solution of (S)-benzyl 4-(3-(tert-butoxycarbonylamino)-2-oxopyrrolidin-1-yl)piperidine-1-carboxylate (Preparation E, Step C, 7.0 g, 17 mmol) in methanol (300 mL) purged with nitrogen was added Pd/C (10%, 2 g) and the reaction was stirred overnight at ambient temperature under a balloon of hydrogen gas. The reaction was next purged with nitrogen and filtered through Celite®, and the filter cake was washed with methanol (about 100 mL). The combined organic phases were concentrated under vacuum to yield (S)-tert-butyl 2-oxo-1-(piperidin-4-yl)pyrrolidin-3-ylcarbamate (4.0 g, 83%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754226B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-265402a67edd4d03bff8d83d96d0244d |
| Source note | uspto-grants-2014_06 |