HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → tert-Butyl 4-amino-3-methoxypiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | tert-Butyl 3-methoxy-4-oxopiperidine-1-carboxylate | HCID 57363786 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-Butyl 4-amino-3-methoxypiperidine-1-carboxylate | HCID 53396191 | — |
Reaction Steps
To a solution of 1,1-dimethylethyl 3-(methyloxy)-4-oxo-1-piperidinecarboxylate D18 (2.9 g) in MeOH (100 ml), was added sodium cyanoborohydride (7.9 g, 126 mmol) and ammonium acetate (9.7 g, 126 mmol) at R.T. The reaction mixture was stirred for 4 hours. The resulting mixture was concentrated in vacuo, dissolved in water, basified with sodium hydroxide to pH10 and extracted with DCM. The organic layer was dried over anhydrous MgSO4, concentrated in vacuo to get the desired product D19 in 2.85 g. LCMS [MH+] [email protected] min (5 min run)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045485B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-39b0db23f22f48d08747b3ea32266c1e |
| Source note | uspto-grants-2015_06 |