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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1447804Erstellt: 25. Oktober 2026

4-Methylmorpholine → BOC-MePhe-NHCH2CH2CH2NMe2

https://huagongshe.com/reaction/1447804

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktN,N-Dimethyl-1,3-propanediamineHCID 7993—
EduktBoc-N-Me-Phe-OHHCID 7010602—
LösungsmittelDichloromethaneHCID 6344—
ProduktBOC-MePhe-NHCH2CH2CH2NMe2HCID 131711662—

Reaktionsschritte

N-t-Butyloxycarbonyl-N-methylphenylalanine (2.79 g) and NMM (1.01 g) were dissolved in dichloromethane (20 ml) and the stirred solution cooled to -20° IBCF (1.37 g) was then added and the mixture stirred for 5 minutes before the addition of NH2CH2CH2CH2NMe2 (1.02 g). The solution was stirred for 1 hour at -20° and then at room temperature for 12 hours. The mixture was evaporated, and the residue dissolved in ethyl acetate (50 ml) and an aqueous solution of sodium bicarbonate (saturated, 50 ml). The ethyl acetate layer was washed with aqueous sodium bicarbonate (saturated, 50 ml), water (2×50 ml) and 10% aqueous citric acid (2×50 ml). The citric acid extracts were combined, made basic with saturated sodium bicarbonate solution, and extracted with ethyl acetate (3×50 ml). The ethyl acetate extracts were combined, dried (Na2SO4) and evaporated to yield the title compound as an oil Rf1E 0.24, Rf3A 0.37.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04178371
Quelldatensatzuspto-grants-1979_12
ORD IDord-f00e84a52ab6457ab47b7b92b699c88c
Quellennotizuspto-grants-1979_12