돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 778생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/778

반응식

참여 물질

역할이름HCID투입량
반응물N-benzyloxycarbonyl-beta-benzyl-L-aspartyl-D-alanineHCID 53966575—
반응물(R)-2-Methoxy-1-phenylethanamine hydrochlorideHCID 66589172—
생성물alpha-L-aspartyl-D-alanine-(R)-alpha-methoxymethylbenzylamideHCID 2288290657.3%

반응 단계

The same process as in Example 15 was repeated, except that N-benzyloxycarbonyl-β-benzyl-L-aspartyl-D-alanine was used in place of N-benzyloxycarbonyl-β-benzyl-L-aspartyl-D-valine and that (R)-α-methoxymethylbenzylamine hydrochloride was used in place of (R)-α-ethoxymethyl benzylamine hydrochloride, and α-L-aspartyl-D-alanine-(R)-α-methoxymethylbenzylamide was obtained as a solid product. The total yield was 57.3%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723165
출처 데이터셋uspto-grants-1998_03
ORD IDord-12a035e31d384b0d952ee7e106393c5e
출처 메모uspto-grants-1998_03