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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2373071Erstellt: 24. Oktober 2026

4-Methylmorpholine → Z-Gly-Leu-PheCH2F

https://huagongshe.com/de/reaction/2373071

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktBenzyloxycarbonylglycineHCID 14349—
EduktSodium HydroxideHCID 14798—
EduktZ-Gly-Leu-OHHCID 96816—
EduktPheCH2F hydrochlorideHCID 131717227—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktZ-Gly-Leu-PheCH2FHCID 13171722954%

Reaktionsschritte

Z-Gly-LeuOH was made by mixed anhydride coupling of Z-GlyOH and LeuOBzl tosylate, followed by NaOH hydrolysis of the benzyl ester. To a solution of Z-Gly-LeuOH (0.223 g, 0.69 mmol) in THF (4 mL) at -20° C. was added NMM (76 uL, 0.69 mmol), followed by IBCF (90 uL, 0.69 mmol). After 10 minutes, a precooled solution of PheCH2F hydrochloride (0.15 g, 0.69 mmol) in DMF (1 mL) was added, followed by a second equivalent (76 uL, 0.69 mmol) of NMM. After 30 minutes of stirring, the mixture was quenched with 1M HCl (5 mL), extracted with ethyl acetate (20 mL), washed with saturated aqueous NaHCO3 (6 mL), brine (5 mL), dried over MgSO4, filtered, and evaporated to dryness. The residue was crystallized from ether/hexane to give 0.18 g (54%) of Z-Gly-Leu-PheCH2F.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05101068
Quelldatensatzuspto-grants-1992_03
ORD IDord-1a2cdad7a44c445db5cfed2e12ca1dee
Quellennotizuspto-grants-1992_03