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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 774생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물N-benzyloxycarbonyl-beta-benzyl-L-aspartyl-D-valine (R)-alpha-methoxymethylbenzylamideHCID 53886295—
촉매HCID 178418390HCID 178418390—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물alpha-L-aspartyl-D-valine (R)-alpha-methoxymethylbenzylamideHCID 1179321770.1%

반응 조건

온도40 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723165
출처 데이터셋uspto-grants-1998_03
ORD IDord-1b033c485fa54b2cb55a6e97a581a99c
출처 메모uspto-grants-1998_03