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HRID 45622作成日:2026年10月25日

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/reaction/45622

反応式

関与物質

役割名称HCID仕込み量
反応物methyl (2S)-2-[[(1R)-1-(1-benzofuran-5-yl)-2-oxo-2-(2-phenylmethoxyanilino)ethyl]amino]-4-methylpentanoateHCID 45076860—
触媒PalladiumHCID 23938—
溶媒Ethyl AcetateHCID 8857—
生成物methyl N-{(1R)-1-(benzofuran-5-yl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinateHCID 4507685982%

反応手順

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).

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-c5c4efe93d3946e0893ac25a23b38fcc
出典メモuspto-grants-2013_09