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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 461788Erstellt: 25. Oktober 2026

4-Methylmorpholine → Acetylalanylalanylleucyl-2-azaalanyl-DL-lactic acid ethyl ester

https://huagongshe.com/reaction/461788

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktIsobutyl chloroformateHCID 62365—
EduktAcetylalanylalanylleucineHCID 54064604—
Edukt2-Azaalanyl-dl-lactic acid ethyl esterHCID 131710980—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktAcetylalanylalanylleucyl-2-azaalanyl-DL-lactic acid ethyl esterHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04064236
Quelldatensatzuspto-grants-1977_12
ORD IDord-7ce4ed708b4e47e69982573dd8c2ccc5
Quellennotizuspto-grants-1977_12