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HRID 45612作成日:2026年10月26日

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/reaction/45612

反応式

関与物質

役割名称HCID仕込み量
反応物methyl N-[(1R)-2-{[2-(benzyloxy)phenyl]amino}-1-(2,4-difluorophenyl)-2-oxoethyl]-L-leucinateHCID 45076862—
触媒PalladiumHCID 23938—
溶媒Ethyl AcetateHCID 8857—
生成物methyl N-{(1R)-1-(2,4-difluorophenyl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinateHCID 4507686192.4%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541579B2
出典データセットuspto-grants-2013_09
ORD IDord-a3e3e7397f4846cea037d095faf831f0
出典メモuspto-grants-2013_09