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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588329Generated: October 30, 2026

Ethanol → Sacubitril N-Boc Ester

https://huagongshe.com/reaction/588329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant(R)-5-Biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylenepentanoic acid ethyl esterHCID 66958146—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTriethylamineHCID 8471—
ProductSacubitril N-Boc EsterHCID 58160380—

Reaction Steps

500 mg (R)-5-Biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylenepentanoic acid ethyl ester (2-a, R1=Boc, R2=H, R3=CO2Et) is added to ethanol (5 ml) at ambient temperature. Triethylamine (170 μl) is then added to the mixture. 50 mg Palladium on carbon (10%, 50% water-wet, Degussa E101 NE/W) is then added. Hydrogen gas at ambient pressure is applied to the mixture. The mixture is then stirred overnight at ambient temperature and pressure. The mixture is then filtered and concentrated under reduced pressure to afford 2R,4S)-5-Biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylpentanoic acid ethyl ester (1-a, R1=Boc, R2=H, R3=CO2Et) and (2S,4S)-5-biphenyl-4-yl-4-tert-butoxycarbonylamino-2-methylpentanoic acid ethyl ester (1-b, R1=Boc, R2=H, R3=CO2Et). Spectroscopic data as in Example 63. Ratio of diastereomers 70:30 (1-a, R1=Boc, R2=H, R3=CO2Et: 1-b, R1=Boc, R2=H, R3=CO2Et) as determined by hplc (hplc method as in Example 65)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227934B2
Source datasetuspto-grants-2016_01
ORD IDord-6c8dd0e898c84edd828db2527911bd3b
Source noteuspto-grants-2016_01