HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22942118, compound → HCID 22942119, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 22942118 | HCID 22942118 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | HCID 22942119 | HCID 22942119 | 97.8% |
Reaction Steps
A solution of 230 mg (0.223 mmol) of N-[N-[N-[N-[N-[3-(tert-butoxycarbonyl)propionyl]-O-tert-butyl-L-α-aspartyl]-O-tert-butyl-L-α-glutamyl]-2-methyl-L-phenylalanyl]-3-methyl-L-valyl]-3-cyclopentyl-L-alanine benzyl ester in 10 ml of dimethylformamidewas hydrogenated over 25 mg of 10% palladium/carbon for 3 hours. The catalyst was removed by filtration, the filtrate was evaporated and the residue was triturated with diethyl ether to give 206 mg of N-[N-[N-[N-[N-[3-(tert-butoxycarbonyl)propionyl]-O-tert-butyl-L-α-aspartyl]-O-tert-butyl-L-α-glutamyl]-2-methyl-L-phenylalanyl]-3-methyl-L-valyl]-3-cyclopentyl-L-alanine as a white solid; MS: m/e 944 [M+H].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05866684 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-2caf32eaad694a7aae59ccb1e4120172 |
| Source note | uspto-grants-1999_02 |