HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20522503, compound → L-Alanine, N-acetyl-L-phenylalanyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20522503 | HCID 20522503 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | L-Alanine, N-acetyl-L-phenylalanyl- | HCID 11196700 | 101.7% |
Reaction Steps
According to the same procedure as in Example 1, 1-(1-methoxycarbonylethyl)-3-acetylamino-4-phenylazetidin-2-one (400 mg.) was subjected to hydrogenolysis at 50° C. in ethanol (30 ml.) under a hydrogen pressure of one atmosphere in the presence of a 10% Pd-C (580 mg.). The reaction was completed in 7 hours. The same after-treatment as in Example 1 was followed to give methyl ester of N-acetylphenylalanylalanine (390 mg., yield: 96.8%) melting at 147.0°-155.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04352752 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-ce412dd891a94094b7d338bc4c9c0ca3 |
| Source note | uspto-grants-1982_10 |