HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Methylmorpholine → Acetylalanylalanylleucyl-2-azaalanyl-DL-lactic acid ethyl ester
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Methylmorpholine | HCID 7972 | — |
| Edukt | Isobutyl chloroformate | HCID 62365 | — |
| Edukt | Acetylalanylalanylleucine | HCID 54064604 | — |
| Edukt | 2-Azaalanyl-dl-lactic acid ethyl ester | HCID 131710980 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Acetylalanylalanylleucyl-2-azaalanyl-DL-lactic acid ethyl ester | HCID 131710982 | — |
Reaktionsschritte
Acetylalanylalanylleucine (1.5 mmole) and N-methylmorpholine (3 mmole) are dissolved in methylene chloride (10 ml) and diluted with dry tetrahydrofuran (250 ml) and cooled to -20° to -25°. Isobutyl chloroformate (1.5 mmole) is added with stirring and the mixture is stirred for 10 minutes. A solution of 2-azaalanyl-dl-lactic acid ethyl ester (1.5 mmole, Example 5, Step A) in tetrahydrofuran (3 ml) is added and the mixture is allowed to warm to room temperature over a period of 2 hours and stirred overnight. The precipitate is filtered off and the filtrate is evaporated to dryness. Chromatography on silica gel (25 gm) and elution with 12% methanol in chloroform gives acetylalanylalanylleucyl-2-azaalanyl-dl-lactic acid ethyl ester.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04064236 |
| Quelldatensatz | uspto-grants-1977_12 |
| ORD ID | ord-7ce4ed708b4e47e69982573dd8c2ccc5 |
| Quellennotiz | uspto-grants-1977_12 |