HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → (S)-tert-butyl 3-((3-aminopyridin-4-yl)oxy)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | tert-butyl(3S)-3-[(3-nitro-4-pyridyl)oxy]piperidine-1-carboxylate | HCID 86720990 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (S)-tert-butyl 3-((3-aminopyridin-4-yl)oxy)piperidine-1-carboxylate | HCID 86720991 | 102.3% |
Reaction Steps
Pd on C, (10%, wet, Degussa) (1 g, 0.9397 mmol) was added to a stirred solution of tert-butyl (3S)-3-[(3-nitro-4-pyridyl)oxy]piperidine-1-carboxylate (2.65 g, 8.196 mmol) in EtOAc (30 mL)/EtOH (15 mL). The reaction was placed under an atmosphere of hydrogen and stirred at ambient temperature for 16 hours. The catalyst was removed by filtration through a pad of celite and the filtrate concentrated in vacuo to give the sub-title compound as an off-white solid (2.46 g, >100% Yield). MS (2ES+) 587.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340546B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-8b2bb26d32494b96a9a59da65df3c9f9 |
| Source note | uspto-grants-2016_05 |