HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → HCID 53789352, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | HCID 54166524 | HCID 54166524 | — |
| Reactant | HCID 54434155 | HCID 54434155 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 53789352 | HCID 53789352 | — |
Reaction Steps
A solution of t-butoxycarbonyl-glycyl-asparaginyl-phenylalanyl-phenylalanine methyl ester (0.525 g, 0.879 mmole, described in Example 4) in trifluoroacetic acid (10 ml) is stirred at 0° C. for 90 minutes and evaporated. The residue is dissolved in methanol (1 ml) and diethyl ether (100 ml) is added. The precipitate is collected and dried. A solution of the precipitate, N-ethylmorpholine (0.11 ml, 0.85 mmole) and 3-tritylthiopropionic acid pentachlorophenyl ester (0.556 g, 0.935 mmole) in dimethylformamide (25 ml) is stirred at 0° C. for 1 hour and at 25° C. for 20 hours and evaporated. The residue is triturated with methanol and the precipitate is dried to give the title compound as a powder, mp 234°-236.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04118380 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-8e0830ca757b4c4383eacd2652fa07ac |
| Source note | uspto-grants-1978_10 |