HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl (1-benzylpiperidin-4-yl)methylcarbamate → 4-N-Boc-4-N-Methyl-aminopiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl (1-benzylpiperidin-4-yl)methylcarbamate | HCID 18476608 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-N-Boc-4-N-Methyl-aminopiperidine | HCID 2756806 | 85% |
Reaction Steps
tert-Butyl 1-benzylpiperidin-4-yl(methyl)carbamate (1.0 g, 3.289 mmol, 1.0 eq.) was dissolved in MeOH (15 ml) and degassed with argon. Pd/C (300 mg) was then added and hydrogenation was carried out for 4 hours. After monitoring by TLC, the reaction mixture was filtered over Celite and the filtrate was concentrated under reduced pressure. The crude product was used in the next stage without being purified further. Yield: 85% (600 mg, 2.803 mmol)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680159B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-7367616cf3984297a5c4518a2954ef88 |
| Source note | uspto-grants-2014_03 |