HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium formate → (R)-tert-butyl 3-(2-amino-5-fluorophenoxy)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | (R)-tert-butyl 3-(5-fluoro-2-nitrophenoxy)piperidine-1-carboxylate | HCID 67395513 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (R)-tert-butyl 3-(2-amino-5-fluorophenoxy)piperidine-1-carboxylate | HCID 58413198 | — |
Reaction Steps
Amoniumformiate (1.0 g) was added into a suspension of (R)-tert-butyl 3-(5-fluoro-2-nitrophenoxy)piperidine-1-carboxylate and palladium on charcoal (125.0 mg) in anhydrous MeOH (10.0 ml) at room temperature. The reaction was stirred at room temperature overnight when LCMS analysis indicated consumption of the starting material. The solution was filtered through celite and washed with MeOH. The filtrate was concentrated in vacuo. The residue was triturated with diethylether to remove the ammoniumformiate residues. The solution was filtered and concentrated in vacuo. The residue was purified by chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08648068B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-250dd16659d04b508156aa1c00a196e2 |
| Source note | uspto-grants-2014_02 |