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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 774Erstellt: 23. Oktober 2026

N-benzyloxycarbonyl-beta-benzyl-L-aspartyl-D-valine (R)-alpha-methoxymethylbenzylamide → alpha-L-aspartyl-D-valine (R)-alpha-methoxymethylbenzylamide

https://huagongshe.com/de/reaction/774

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-benzyloxycarbonyl-beta-benzyl-L-aspartyl-D-valine (R)-alpha-methoxymethylbenzylamideHCID 53886295—
KatalysatorHCID 178418390HCID 178418390—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produktalpha-L-aspartyl-D-valine (R)-alpha-methoxymethylbenzylamideHCID 1179321770,1%

Reaktionsbedingungen

Temperatur40 °C

Reaktionsschritte

To a suspension of 6.20 g (10.5 mmols) of N-benzyloxycarbonyl-β-benzyl-L-aspartyl-D-valine (R)-α-methoxymethylbenzylamide in 200 ml of methanol and 50 ml of water was added 1.50 g of 10% Pd-carbon (water content 50%). The mixture was reduced under hydrogen under heat at 40° C. The catalyst was removed by filtration, and the resulting filtrate was concentrated under reduced pressure to 15 ml. The crystal thus precipitated was removed by filtration and dried to obtain 2.69 g (7.36 mmols, 70.0% ) of α-L-aspartyl-D-valine (R)-α-methoxymethylbenzylamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723165
Quelldatensatzuspto-grants-1998_03
ORD IDord-1b033c485fa54b2cb55a6e97a581a99c
Quellennotizuspto-grants-1998_03