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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45622생성일: 2026년 10월 23일

methyl (2S)-2-[[(1R)-1-(1-benzofuran-5-yl)-2-oxo-2-(2-phenylmethoxyanilino)ethyl]amino]-4-methylpentanoate → methyl N-{(1R)-1-(benzofuran-5-yl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinate

https://huagongshe.com/ko/reaction/45622

반응식

참여 물질

역할이름HCID투입량
반응물methyl (2S)-2-[[(1R)-1-(1-benzofuran-5-yl)-2-oxo-2-(2-phenylmethoxyanilino)ethyl]amino]-4-methylpentanoateHCID 45076860—
촉매PalladiumHCID 23938—
용매Ethyl AcetateHCID 8857—
생성물methyl N-{(1R)-1-(benzofuran-5-yl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinateHCID 4507685982%

반응 단계

A mixture of palladium on carbon (10%, 500 mg), methyl N-[(1R)-2-{[2-(benzyloxy)phenyl]amino}-1-(benzofuran-5-yl)-2-oxoethyl]-L-leucinate (5.1 g) and ethyl acetate (60 ml) was stirred under a hydrogen atmosphere for 5 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-(benzofuran-5-yl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinate (3.429 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541579B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-c5c4efe93d3946e0893ac25a23b38fcc
출처 메모uspto-grants-2013_09