HuagongsheHuagongshe Chemistry Print Report · For research reference only
N2 [3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-(2-naphthyl)butyl]-N1-tert.butyl-L-prolinamide → N2 [3(S)-amino-2(R)-hydroxy-L-(2-naphthyl)butyl]-N1-tert.butyl-L-prolinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N2 [3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-(2-naphthyl)butyl]-N1-tert.butyl-L-prolinamide | HCID 86746265 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N2 [3(S)-amino-2(R)-hydroxy-L-(2-naphthyl)butyl]-N1-tert.butyl-L-prolinamide | HCID 86746264 | 98.8% |
Reaction Steps
A solution of 0.725 g of N2 -[3(S)-(benzyloxyformamido)-2(R)-hydroxy-4-(2-naphthyl)butyl]-N1 -tert.butyl-L-prolinamide was dissolved in 25 ml of ethanol and hydrogenated at room temperature and under atmospheric pressure over 0.5 g of 10% palladium-on-carbon for 20 hours. The catalyst was filtered off and the filtrate was evaporated to give 0.54 g of N2 -[3(S)-amino-2(R)-hydroxy-L-(2-naphthyl)butyl]-N1 -tert.butyl-L-prolinamide as a white foam which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05652369 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-c218a31d73d74f4f8ebc991cd2b74d0a |
| Source note | uspto-grants-1997_07 |