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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 47046Erstellt: 25. Oktober 2026

Ethylmorpholine → N-ethoxycarbonyl-L-alanyl-L-proline ethylamide

https://huagongshe.com/reaction/47046

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylmorpholineHCID 7525—
EduktEthyl chloroformateHCID 10928—
EduktL-alanyl-L-proline ethylamide hydrobromideHCID 70602162—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-ethoxycarbonyl-L-alanyl-L-proline ethylamideHCID 5440244647%

Reaktionsschritte

2 g (0.0066 mol) of L-alanyl-L-proline ethylamide hydrobromide were suspended in 20 ml of dry tetrahydrofuran, 1.84 ml (0.0145 mol) of N-ethylmorpholine and 0.76 ml (0.0079 mol) of ethyl chloroformate were added and the mixture was stirred at room temperature for 2 hours. The solvent was evaporated off and the residue dissolved in 100 ml of chloroform and washed successively with 2-N hydrochloric acid in brine, brine, saturated sodium bicarbonate solution and brine, dried over magnesium sulphate and evaporated to an oil which soon crystallised. Recrystallisation from chloroform/petrol yielded 0.88 g (47%) of N-ethoxycarbonyl-L-alanyl-L-proline ethylamide of melting point 126°-128° C.; [α]D20 =-117.6° (c=1.02% in methanol).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04176116
Quelldatensatzuspto-grants-1979_11
ORD IDord-3b7eb8016c7d444da66bd7e1e242c8e2
Quellennotizuspto-grants-1979_11