HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Perindopril
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | (2S,3aS,7aS)-1-[(2S)-2-[[(1S)-1-(Ethoxycarbonyl)butyl]amino]-1-oxopropyl]octahydro-1H-indole-2-carboxylic Acid Benzyl Ester | HCID 71751530 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | Perindopril | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07456296B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-d43390b073ae43a1b585a6872cc18615 |
| Source note | uspto-grants-2008_11 |