HuagongsheHuagongshe Chemistry Print Report · For research reference only
benzyl{(1S)-3-[(tert-butoxycarbonyl)amino]-1-[({3-[(tert-butoxycarbonyl)amino]-2-hydroxypropyl}amino)carbonyl]propyl}carbamate → Tert-butyl[3-({(2s)-2-amino-4-[(tert-butoxycarbonyl)amino]butanoyl}amino)-2-hydroxypropyl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | benzyl{(1S)-3-[(tert-butoxycarbonyl)amino]-1-[({3-[(tert-butoxycarbonyl)amino]-2-hydroxypropyl}amino)carbonyl]propyl}carbamate | HCID 131727150 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Tert-butyl[3-({(2s)-2-amino-4-[(tert-butoxycarbonyl)amino]butanoyl}amino)-2-hydroxypropyl]carbamate | HCID 89225963 | — |
Reaction Steps
38 mg (0.12 mmol) of the compound from Example 98A are dissolved in 10 ml of methanol, and 10 mg of palladium on activated carbon (10%) are added. The mixture is hydrogenated under atmospheric pressure for 2 h and filtered through kieselguhr, and the mother liquor is concentrated in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07446102B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-2ca48361dea845028d87750143e1add3 |
| Source note | uspto-grants-2008_11 |