HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22942128, compound → HCID 86753708, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 22942128 | HCID 22942128 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Piperidine | HCID 8082 | — |
| Product | HCID 86753708 | HCID 86753708 | — |
Reaction Steps
A solution of 10.088 g (9.4 mmol) of N-[N-[N-[N-[N-[(9-fluorenyl)methoxycarbonyl] O-tert-butyl-L-α-aspartyl]-O-tert-butyl-L-α-glutamyl]-2-methyl-L-phenylalanyl]-3-methyl-L-valyl]-L-leucine benzyl ester in 30 ml of piperidine and 120 ml of dichloromethane was stirred for 30 minutes at room temperature. The solvent was removed by evaporation and the residue was chromatographed on silica gel using firstly 20% ethyl acetate in hexane and then 10% methanol in dichloromethane for the elution. Evaporation gave N-[N-[N-[N-[O-tert-butyl-L-α-aspartyl]-O-tert-butyl-L-α-glutamyl-2-methyl-L-phenylalanyl]-3-methyl-L-valyl-L-leucine benzyl ester in the form of an oil which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05866684 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-2fbc72ecd0f74ca5b9e12b3a92152827 |
| Source note | uspto-grants-1999_02 |