HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → 1-tert-butyl 3-ethyl (3S,4R)-4-aminopiperidine-1,3-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | (3S,4R)-1-tert-butyl 3-ethyl 4-((R)-1-phenylethylamino)-piperidine-1,3-dicarboxylate | HCID 66952586 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-tert-butyl 3-ethyl (3S,4R)-4-aminopiperidine-1,3-dicarboxylate | HCID 58745494 | 96% |
Reaction Steps
A solution of 252C (2.6 g, 6.9 mmol) in EtOH (100 mL) was treated with ammonium formate (3.5 g, 55.3 mmol) and 10% Pd/C (390 mg). The reaction mixture was heated to reflux under a nitrogen atmosphere for three hours. The resulting suspension was filtered through a pad of celite and concentrated in vacuo to afford 1.8 g (yield: 96%) Compound 259A as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07297695B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-9c540fb60d6c473db1bcc5f56668afb6 |
| Source note | uspto-grants-2007_11 |