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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2108697생성일: 2026년 10월 23일

methyl N-[(1R)-2-{[2-(benzyloxy)phenyl]amino}-1-(2,4-difluorophenyl)-2-oxoethyl]-L-leucinate → methyl N-{(1R)-1-(2,4-difluorophenyl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinate

https://huagongshe.com/ko/reaction/2108697

반응식

참여 물질

역할이름HCID투입량
반응물methyl N-[(1R)-2-{[2-(benzyloxy)phenyl]amino}-1-(2,4-difluorophenyl)-2-oxoethyl]-L-leucinateHCID 45076862—
촉매PalladiumHCID 23938—
용매Ethyl AcetateHCID 8857—
생성물methyl N-{(1R)-1-(2,4-difluorophenyl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinateHCID 4507686192.4%

반응 단계

A mixture of palladium on carbon (10%, 300 mg), methyl N-[(1R)-2-{[2-(benzyloxy)phenyl]amino}-1-(2,4-difluorophenyl)-2-oxoethyl]-L-leucinate (2.88 g) and ethyl acetate (30 ml) was stirred under a hydrogen atmosphere for 3 hours. The reaction was then filtered through Celite and the filter pad was washed with further portions of ethyl acetate. The combined organic fractions were evaporated to give methyl N-{(1R)-1-(2,4-difluorophenyl)-2-[(2-hydroxyphenyl)amino] -2-oxoethyl}-L-leucinate (2.179 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07514437B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-5a8d2e628cf64376b8a98d17383cf164
출처 메모uspto-grants-2009_04