HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → (S)-1-N-Boc-Piperidine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | (2S)-1-((tert-butoxy)carbonyl)piperidine-2-carboxylic acid | HCID 688617 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S)-1-N-Boc-Piperidine-2-carboxamide | HCID 2756821 | 95% |
Reaction Steps
Anhydrous ammonia gas was bubbled through a solution of (S)-(−)-1-(tert-butoxycarbonyl)-2-piperidine carboxylic acid (500 mg, 2.18 mmol) in DMF (50 ml) for 15 minutes. PyBop (1.25 g, 2.40 mmol) was added. After 5 hours, solvent was evaporated under reduced pressure. A solution of the resultant residue in ethyl acetate was washed with 5% citric acid (50 ml×3), 1 N NaOH (50 ml×3), dried with MgSO4, filtered, and concentrated to give 450 mg of (S)-2-carbamoyl-piperidine-1-carboxylic acid tert-butyl ester as a clear oil in 95% yield, which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06720346B2 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-fdd276dbdb014263959dff5cc73405d8 |
| Source note | uspto-grants-2004_04 |