HuagongsheHuagongshe Chemistry Print Report · For research reference only
N2 [3(S)-[[N-[4-(benzyloxycarbonyl)benzoyl]-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1-tert.butyl-L-prolinamide → HCID 86746240, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N2 [3(S)-[[N-[4-(benzyloxycarbonyl)benzoyl]-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1-tert.butyl-L-prolinamide | HCID 86746242 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 86746240 | HCID 86746240 | 80.6% |
Reaction Steps
274 mg of N2 -[3(S)-[[N-[4-(benzyloxycarbonyl)-benzoyl]-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide in 100 ml of isopropanol were hydrogenated over 10% palladium-on-carbon at 20° C. and under atmospheric pressure for 16 hours. The catalyst was removed by filtration and the filtrate was evaporated to give 193 mg of N2 -[3(S)-[[N-(4-carboxybenzoyl)-L-asparaginyl]amino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-L-prolinamide as a white solid from methanol/ethylacetate: MS: m/e 596 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05446161 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-38219999574347df8f40ec801a63856e |
| Source note | uspto-grants-1995_08 |