HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl{(1S)-4-[(tert-butoxycarbonyl)amino]-1-[({(4S)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentyl}amino)carbonyl]butyl}carbamate → N5-(tert-Butoxycarbonyl)-N-{(4S)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentyl}-L-ornithinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl{(1S)-4-[(tert-butoxycarbonyl)amino]-1-[({(4S)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentyl}amino)carbonyl]butyl}carbamate | HCID 86625287 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N5-(tert-Butoxycarbonyl)-N-{(4S)-4-[(tert-butoxycarbonyl)amino]-5-hydroxypentyl}-L-ornithinamide | HCID 86619441 | — |
Reaction Steps
30 mg of palladium on activated carbon (10%) are added to a mixture of 0.164 g (0.29 mmol) of the compound from Example 248A 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-3057f601b94b4d54af34d1cdd699eb3b |
| Source note | uspto-grants-2008_11 |