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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 770Erstellt: 23. Oktober 2026

N-benzyloxycarbonyl-beta-benzyl-L-aspartyl-D-isoleucine (S)-alpha-ethylbenzylamide → alpha-L-aspartyl-D-isoleucine (S)-alpha-ethylbenzylamide

https://huagongshe.com/de/reaction/770

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-benzyloxycarbonyl-beta-benzyl-L-aspartyl-D-isoleucine (S)-alpha-ethylbenzylamideHCID 53679369—
KatalysatorHCID 178418390HCID 178418390—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
Produktalpha-L-aspartyl-D-isoleucine (S)-alpha-ethylbenzylamideHCID 5426267272,3%

Reaktionsschritte

To a suspension of 2.81 g (4.7 mmols) of N-benzyloxycarbonyl-β-benzyl-L-aspartyl-D-isoleucine (S)-α-ethylbenzylamide in 150 ml of methanol and 50 ml of water was added 2.0 g of 10% Pd-carbon (water content 50%). The mixture was reduced under hydrogen at room temperature for 5 hours. The catalyst was removed by filtration, and the resulting filtrate was concentrated under reduced pressure to be 20 ml. The crystals thus precipitated were taken out by filtration and dried to obtain 1.22 g (3.4 mmols) of α-L-aspartyl-D-isoleucine (S)-α-ethylbenzylamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05723165
Quelldatensatzuspto-grants-1998_03
ORD IDord-b4a1a9f06c874053b3ad0f85aaa15884
Quellennotizuspto-grants-1998_03