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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588306Generated: October 27, 2026

(R)-5-biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylenepentanoic acid → (2R,4S)-2-methyl-4-((2-methylpropan-2-yl)oxycarbonylamino)-5-(4-phenylphenyl)pentanoic acid

https://huagongshe.com/reaction/588306

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-5-biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylenepentanoic acidHCID 46193439—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventIsopropyl AcetateHCID 7915—
Product(2R,4S)-2-methyl-4-((2-methylpropan-2-yl)oxycarbonylamino)-5-(4-phenylphenyl)pentanoic acidHCID 46193546—

Reaction Steps

20 mg (R)-5-Biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylenepentanoic acid (2-a, R1=Boc, R2=H, R3=CO2H) is added to isopropyl acetate (400 μl). 10% Platinum on carbon (2 mg) is then added. Hydrogen gas at ambient pressure is applied to the mixture. The mixture is stirred at ambient temperature and pressure overnight. The mixture is then filtered over Celite and washed with isopropyl acetate (2×0.5 ml). The mixture is then concentrated in vacuo to give (2R,4S)-5-biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylpentanoic acid (1-a, R1=Boc, R2=H, R3=CO2H) and (2S,4S)-5-biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylpentanoic acid (1-b, R1=Boc, R2=H, R3=CO2H). Spectroscopic data as in Example 40, Method 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227934B2
Source datasetuspto-grants-2016_01
ORD IDord-9a43ec66fea143ba8914fbf7921f5fd5
Source noteuspto-grants-2016_01