HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → (S)-tert-butyl 1-amino-3-cyclopropyl-1-oxopropan-2-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | (S)-2-((tert-Butoxycarbonyl)amino)-3-cyclopropylpropanoic acid | HCID 5706350 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (S)-tert-butyl 1-amino-3-cyclopropyl-1-oxopropan-2-ylcarbamate | HCID 70082562 | 78% |
Reaction Steps
A mixture of (S)-2-(tert-butoxycarbonylamino)-3-cyclopropylpropanoic acid (CAN 89483-06-7, 10 g, 44 mmol), di-tert-butyl dicarbonate (CAN:24424-99-5, 14.28 g, 66 mmol) and pyridine (2.4 mL) in acetonitrile (200 mL) was stirred at room temperature for 20 min. Ammonia (10 mL) was added dropwise for 20 min. The resulting reaction mixture was stirred for 4 h. During removal of most of the solvent under reduced pressure the product precipitated and the solid was filtered off and washed with acetonitrile (20 mL). The solid was dried under reduced pressure to give the title compound (7.73 g, 78%) as white solid; MS (EI): m/e 251.2 [M+Na]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09303012B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-3d6210924cbb44549b69d168bacf4b68 |
| Source note | uspto-grants-2016_04 |