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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383964Generated: October 25, 2026

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/383964

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl N-[(1R)-2-{[2-(benzyloxy)phenyl]amino}-1-(2,4-difluorophenyl)-2-oxoethyl]-L-leucinateHCID 45076862—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Productmethyl N-{(1R)-1-(2,4-difluorophenyl)-2-[(2-hydroxyphenyl)amino]-2-oxoethyl}-L-leucinateHCID 4507686192.4%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367673B2
Source datasetuspto-grants-2013_02
ORD IDord-a07cc40113874b4e88eafedefca654ea
Source noteuspto-grants-2013_02