HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Azide → tert-butyl (3S)-3-aminopiperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | tert-Butyl (3R)-3-[(methanesulfonyl)oxy]piperidine-1-carboxylate | HCID 29939737 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-butyl (3S)-3-aminopiperidine-1-carboxylate | HCID 1501975 | — |
Reaction Steps
Sodium azide (7.65 g, 118 mmol) was added to a solution of 1,1-dimethylethyl (3R)-3-[(methylsulfonyl)oxy]-piperidine-1-carboxylate (21.9 g, 78.5 mmol) in dry dimethylformamide (120 mL) and the resultant suspension heated at 70° C. for 48 hours. After cooling to room temperature, the reaction mixture was diluted with water and extracted into ethyl acetate. The organic phase was washed two further times with water, then brine. The organic extracts were dried (MgSO4), filtered and evaporated in vacuo to give an oil. This was purified by flash chromatography on silica, eluting with ethyl acetate/cyclohexane (10:90 to 50:50), to give the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432280B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-78e84d22302c4761b6711cd543c23308 |
| Source note | uspto-grants-2008_10 |