HuagongsheHuagongshe Chemistry Print Report · For research reference only
N2 (benzyloxycarbonyl)-4(R)-(tert-butoxyformamido)-N1-tert.butyl-L-prolinamide → 4(R)-(tert-butoxyformamido)-N1-tert.butyl-L-prolinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N2 (benzyloxycarbonyl)-4(R)-(tert-butoxyformamido)-N1-tert.butyl-L-prolinamide | HCID 86746286 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4(R)-(tert-butoxyformamido)-N1-tert.butyl-L-prolinamide | HCID 57267270 | 106.6% |
Reaction Steps
0.25 g of N2 -(benzyloxycarbonyl)-4(R)-(tert.butoxyformamido)-N1 -tert.butyl-L-prolinamide was dissolved in ethanol and hydrogenated over 0.1 g of 10% palladium-on-carbon at room temperature and under atmospheric pressure for 4 hours. The catalyst was filtered off and the filtrate-was evaporated to give 0.17 g of 4(R)-(tert.butoxyformamido)-N1 -tert.butyl-L-prolinamide as a glass which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05620987 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-ba243995ae504e87a95d2bf1247b3b12 |
| Source note | uspto-grants-1997_04 |