HuagongsheHuagongshe Chemistry Print Report · For research reference only
N2 [3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-phenylbutyl]-4(R)-(tert.butoxyformamido)-N1-tert.butyl-L-prolinamide → N2 [3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-4(R)-(tert.butoxyformamido)-N1-tert-butyl-L-Prolinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N2 [3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-phenylbutyl]-4(R)-(tert.butoxyformamido)-N1-tert.butyl-L-prolinamide | HCID 86746290 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N2 [3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-4(R)-(tert.butoxyformamido)-N1-tert-butyl-L-Prolinamide | HCID 86746288 | 99% |
Reaction Steps
0.22 g of N2 -[3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-phenylbutyl]-4(R)-(tert.butoxyformamido)-N1 -tert.butyl-L-prolinamide was dissolved in 10 ml of ethanol and hydrogenated over 0.05 g of 10% palladium-on-carbon at room temperature and under atmospheric pressure for 2 hours. The catalyst was filtered off and the filtrate was evaporated to give 0.17 g of N2 -[3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-4(R)-(tert.butoxyformamido)-N1 -tert.butyl-L-prolinamide as a gum which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05446161 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-087284a098e94b49abfa22d85aed7be2 |
| Source note | uspto-grants-1995_08 |