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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273477Generated: October 25, 2026

Water → Perindopril

https://huagongshe.com/reaction/273477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant(2S,3aS,7aS)-1-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)butyl]amino]-1-oxopropyl]octahydro-1H-indole-2-carboxylic Acid Benzyl EsterHCID 71751530—
CatalystPalladiumHCID 23938—
SolventCyclohexaneHCID 8078—
ProductPerindoprilHCID 107807—

Reaction Steps

The Perindopril benzyl ester (20 g, 0.0436 moles) was dissolved in cyclohexane (80 ml) in a round bottom flask and the resulting solution was transferred into a hydrogenation bottle. To this was added 10% Palladium on carbon (10% loading), followed by water (70 ml). The reaction mixture was hydrogenated at 27° C. for 3 hrs, under 60 psi pressure when the reaction was complete. The reaction mixture was filtered off and the residue was washed with cyclohexane (20 ml). The filtrate was allowed to settle for 15 min. The aqueous phase was separated. It was washed with cyclohexane (20 ml, twice). Perindopril was isolated in an amount of 11.5 g (71.5%) from the aqueous layer by freeze drying.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456296B2
Source datasetuspto-grants-2008_11
ORD IDord-d43390b073ae43a1b585a6872cc18615
Source noteuspto-grants-2008_11