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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 776생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/776

반응식

참여 물질

역할이름HCID투입량
반응물N-benzyloxycarbonyl-beta-benzyl-L-aspartyl-D-valine (R)-alpha-ethoxymethylbenzylamideHCID 54314208—
촉매HCID 178418390HCID 178418390—
용매MethanolHCID 887—
용매WaterHCID 962—
생성물alpha-L-aspartyl-D-valine (R)-alpha-ethoxymethylbenzylamideHCID 5421338550.3%

반응 조건

온도40 °C

반응 단계

To a suspension of 1.20 g (1.99 mmols) of N-benzyloxycarbonyl-β-benzyl-L-aspartyl-D-valine (R)-α-ethoxymethylbenzylamide in 50 ml of methanol and 10 ml of water was added 0.30 g of 10% Pd-carbon (water content 50%). The mixture was reduced under hydrogen under heat at 40°C., 40 ml of water was added thereto, the catalyst was removed by filtration, and the resulting filtrate was concentrated under reduced pressure to 5 ml. The crystal thus precipitated was removed by filtration and dried to obtain 0.38 g (1.00 mmol, 50.3%) of α-L-aspartyl-D-valine (R)-α-ethoxymethylbenzylamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723165
출처 데이터셋uspto-grants-1998_03
ORD IDord-29bd294101a04d54b49813c6be393808
출처 메모uspto-grants-1998_03