HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-t-butyloxycarbonyl-L-alanyl-L-prolyl-L-proline benzylester → N-t-butyloxycarbonyl-L-alanyl-L-prolyl-L-proline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-t-butyloxycarbonyl-L-alanyl-L-prolyl-L-proline benzylester | HCID 13389836 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-t-butyloxycarbonyl-L-alanyl-L-prolyl-L-proline | HCID 22827655 | 99.8% |
Reaction Steps
N-t-butyloxycarbonyl-L-alanyl-L-prolyl-L-proline benzylester (5.0 g, 10.6 m mole) was dissolved in methanol (100 ml) and hydrogen gas was passed through the solution in the presence of the palladium carbon as a catalyst for 3 hours. The catalyst was removed by filtration and the solvent was distilled off under reduced pressure. Thus obtained residue was dissolved in water and the solution was freeze-dried to give N-t-butyloxycarbonyl-L-alanyl-L-prolyl-L-proline (4.04 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04719200 |
| Source dataset | uspto-grants-1988_01 |
| ORD ID | ord-5f834158ad0144d7b17427348fa3791d |
| Source note | uspto-grants-1988_01 |