Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477455Generated: November 2, 2026

Ethanol → Sacubitril Impurity 3

https://huagongshe.com/reaction/1477455

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantHCID 58160391HCID 58160391—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventTriethylamineHCID 8471—
ProductSacubitril Impurity 3HCID 59318451—
Product2-Pyrrolidinone, 5-([1,1'-biphenyl]-4-ylMethyl)-3-Methyl-, (3R,5S)-HCID 66739158—

Reaction Steps

4 mg (3R/S,5S)-5-Biphenyl-4-ylmethyl-3-iodomethyl-pyrrolidin-2-one (12-a, R1=H, R5=I) is added to ethanol (1 ml) at ambient temperature. Triethylamine (5 μl) is then added to the mixture. 0.4 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 (3R,5S)-5-biphenyl-4-ylmethyl-3-methylpyrrolidin-2-one (3-a, R1=H) and (3S,5S)-5-biphenyl-4-ylmethyl-3-methylpyrrolidin-2-one (3-b, R1=H. Ratio of diastereomers 22:88 (3-a, R1=H to 3-b, R1=H) as determined by nmr. Spectroscopic data for 3-a (R1=H) as for Example 6 in WO/2008/083967. Spectroscopic data for 3-b (R1=H) as for Example 47 in WO/2008/083967.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403766B2
Source datasetuspto-grants-2016_08
ORD IDord-bef14dd85220406a8902ace87224fd43
Source noteuspto-grants-2016_08