HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyloxycarbonyl-prolyl-histidyl-leucine, tert-Butyl Ester → HCID 178445971, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyloxycarbonyl-prolyl-histidyl-leucine, tert-Butyl Ester | HCID 178445970 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178445971 | HCID 178445971 | 116.4% |
Reaction Steps
A mixture of the protected tripeptide of formula III, Z-Pro-His-Leu-OBut (5.9 g, 10.6 mmol, described in Example 2), and 5% palladium on carbon (600 mg) in glacial acetic acid is subjected to hydrogenation. The mixture is filtered and the filtrate evaporated under reduced pressure to give 5.2 g of H-Pro-His-Leu-OBut in the form of its acetate salt. This product is suspended in toluene and the toluene then is removed by distillation so the excess acetic acid is removed azeotropically.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04216209 |
| Source dataset | uspto-grants-1980_08 |
| ORD ID | ord-982213a31ea14dedb9d257f46a607fca |
| Source note | uspto-grants-1980_08 |