HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 4-(2-oxoazepan-1-yl)piperidin-1-carboxylate → 1-(Piperidin-4-yl)azepan-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 4-(2-oxoazepan-1-yl)piperidin-1-carboxylate | HCID 68418576 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(Piperidin-4-yl)azepan-2-one | HCID 68417512 | 101% |
Reaction Steps
To a solution of benzyl 4-(2-oxoazepan-1-yl)piperidin-1-carboxylate (0.25 g) obtained in Example 9a) in ethanol (10 mL) was added 10% palladium on carbon (containing 50% water; 0.03 g), and the mixture was stirred at room temperature for 15 hours under a hydrogen atmosphere. The reaction mixture was filtered, and the solvent was distilled off under reduced pressure to obtain the title compound (0.15 g, quantitative) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745623B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-6fd8d293355045979e6505dd8785f092 |
| Source note | uspto-grants-2010_06 |