HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86753716, compound → HCID 86753715, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86753716 | HCID 86753716 | — |
| Catalyst | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86753715 | HCID 86753715 | 88.8% |
Reaction Steps
0.05 g (0.04 mmol) of (Z)-N2-[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]-N1-[1(S)-(dimethoxymethyl)-3-pentenyl]-L-leucinamide was dissolved in 4 ml of a 1:1 solution of dichloromethane and trifluoroacetic acid containing 3 drops of water. The resulting solution was stirred for 1 hour at room temperature. After removal of the solvent by evaporation the crude product was triturated in diethyl ether to give 0.03 g of (Z)-2(S)-[[N-[N-[N-[N-[N-(3-carboxypropionyl)-L-α-aspartyl]-L-α-glutamyl]-2-methyl-L-phenylalanyl]-3-methyl-L-valyl]-L-leucyl]amino]-4-hexenal as a white solid, MS: m/e 845.7 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06187905B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-f7be088b01b843bda69f8c77018a4343 |
| Source note | uspto-grants-2001_02 |