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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 770생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물N-benzyloxycarbonyl-beta-benzyl-L-aspartyl-D-isoleucine (S)-alpha-ethylbenzylamideHCID 53679369—
촉매HCID 178418390HCID 178418390—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물alpha-L-aspartyl-D-isoleucine (S)-alpha-ethylbenzylamideHCID 5426267272.3%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723165
출처 데이터셋uspto-grants-1998_03
ORD IDord-b4a1a9f06c874053b3ad0f85aaa15884
출처 메모uspto-grants-1998_03