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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1733664Erstellt: 26. Oktober 2026

4-Methylmorpholine → Ethyl N-(1-((benzyloxy)carbonyl)-L-prolyl)-L-leucinate

https://huagongshe.com/reaction/1733664

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktBenzyloxycarbonyl-L-prolineHCID 101987—
EduktL-Leucine, ethyl ester, hydrochloride (1:1)HCID 11658447—
Edukt4-Oxo-3,4-dihydro-3-methanesulfonyloxy-1,2,3-benzotriazineHCID 21896281—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
LösungsmittelEthyl AcetateHCID 8857—
ProduktEthyl N-(1-((benzyloxy)carbonyl)-L-prolyl)-L-leucinateHCID 645307566,4%

Reaktionsschritte

N-Benzyloxycarbonyl-L-proline (1.25 g), L-leucine ethyl ester hydrochloride (1.00 g) and N-methylmorpholine (1.10 ml) are dissolved in chloroform (10 ml) and thereto is added 4-oxo-3,4-dihydro-3-methanesulfonyloxy-1,2,3-benzotriazine (1.20 g). After allowing to stand overnight, to the mixture are added water and ethyl acetate. The ethyl acetate layer is washed and dried, and then the solvent is distilled off to give N-(N-benzyloxycarbonyl-L-prolyl)-L-leucine ethyl ester (1.3 g), melting point: 65°-67° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04242507
Quelldatensatzuspto-grants-1980_12
ORD IDord-89cf0924f3e74005978288a0de1fd424
Quellennotizuspto-grants-1980_12