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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 770Generated: October 23, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-benzyloxycarbonyl-beta-benzyl-L-aspartyl-D-isoleucine (S)-alpha-ethylbenzylamideHCID 53679369—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Productalpha-L-aspartyl-D-isoleucine (S)-alpha-ethylbenzylamideHCID 5426267272.3%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05723165
Source datasetuspto-grants-1998_03
ORD IDord-b4a1a9f06c874053b3ad0f85aaa15884
Source noteuspto-grants-1998_03