HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → Acetylprolylalanylprolyl-2-azaalanyl-l-lactic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | Acetylprolylalanylproline | HCID 14503264 | — |
| Reactant | 2-Azaalanyl-l-lactic acid ethyl ester | HCID 131710977 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Acetylprolylalanylprolyl-2-azaalanyl-l-lactic acid ethyl ester | HCID 131710976 | — |
Reaction Steps
Acetylprolylalanylproline (2 mmole) is dissolved in methylene chloride (5 ml) containing N-methylmorpholine (2 mmole) and diluted with dry tetrahydrofuran (400 ml). To this stirred solution at -20° to -25° is added isobutyl chloroformate (2 mmole) and the mixture is stirred for 15 minutes. A solution of 2-azaalanyl-l-lactic acid ethyl ester (2 mmole) in tetrahydrofuran (2 ml) is then added. The mixture is allowed to warm to room temperature over a period of 1 hour and stirred for a further 3 hours. The mixture is filtered, and the filtrate is evaporated to dryness. Chromatography on silica gel (38 gm) and elution with 5% methanol in chloroform gives acetylprolylalanylprolyl-2-azaalanyl-l-lactic acid ethyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04064236 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-fc573c933d654758865ed101236f25ba |
| Source note | uspto-grants-1977_12 |