HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl{(1S)-4-[(tert-butoxycarbonyl)amino]-1-[({(3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutyl}amino)carbonyl]butyl}carbamate → N5-(tert-Butoxycarbonyl)-N-{(3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutyl}-L-ornithinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl{(1S)-4-[(tert-butoxycarbonyl)amino]-1-[({(3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutyl}amino)carbonyl]butyl}carbamate | HCID 131727168 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N5-(tert-Butoxycarbonyl)-N-{(3S)-3-[(tert-butoxycarbonyl)amino]-4-hydroxybutyl}-L-ornithinamide | HCID 86619439 | — |
Reaction Steps
17 mg of palladium on activated carbon (10%) are added to a mixture of 0.088 g (0.16 mmol) of the compound from Example 238A in 10 ml of ethanol, and the mixture is then hydrogenated under atmospheric pressure for 12 h. The reaction mixture is filtered through kieselguhr, and the filtrate is concentrated in vacuo and dried under high vacuum. The crude product is reacted without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07446102B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-104f176c034a47a08122586e1a4db39e |
| Source note | uspto-grants-2008_11 |