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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383974Generated: October 25, 2026

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/383974

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl (2S)-2-[[(1R)-1-(1-benzofuran-5-yl)-2-oxo-2-(2-phenylmethoxyanilino)ethyl]amino]-4-methylpentanoateHCID 45076860—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Productmethyl N-{(1R)-1-(benzofuran-5-yl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinateHCID 4507685982%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367673B2
Source datasetuspto-grants-2013_02
ORD IDord-bcc91117c1894da0b57c05bce45e4543
Source noteuspto-grants-2013_02