HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → Benzyloxycarbonyl-asparagine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | HCID 86746225 | HCID 86746225 | — |
| Reactant | HCID 86746226 | HCID 86746226 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Product | Benzyloxycarbonyl-asparagine | HCID 75314 | — |
Reaction Steps
In a manner analogous to that described in Example 33, from 0.225 g of dicyclohexylcarbodiimide, 0.135 g of hydroxybenzotriazole, 0.115 g of N-ethylmorpholine, 0.38 g of N2 -[3(S)-amino-2(R)-hydroxy-4-Phenylbutyl]-N1 -benzyl-L-prolinamide and0.266 g of N-(benzyloxycarbonyl)-L-asparagine there was obtained 0.056 g ofN1 -benzyl-N2 -[3(S)-[[N-(benzyloxycarbonyl)-L-asparaginyl] amino]-2(R)-hydroxy-4-phenylbutyl]-L-prolinamide as a white solid: MS: m/e616 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05446161 |
| Source dataset | uspto-grants-1995_08 |
| ORD ID | ord-0e94583ccba6413f886672ad442f7d8a |
| Source note | uspto-grants-1995_08 |