HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Perindopril Benzyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | ethyl (2S)-2-aminopentanoate | HCID 10080526 | — |
| Reactant | benzyl (2S,3aS,7aS)-1-[(2R)-2-bromopropionyl]octahydro-1H-indole-2-carboxylate | HCID 11315392 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Perindopril Benzyl Ester | HCID 11396975 | — |
Reaction Steps
Introduce 123 g of ethyl (2S)-2-aminopentanoate, 160 ml of triethylamine and 160 ml of acetonitrile into a reactor, and then bring the mixture to 60° C., slowly add the solution obtained in Step A and reflux for 4 hours. After returning to ambient temperature, wash the mixture with water and with a dilute acetic acid solution, and then evaporate off the solvents to yield benzyl (2S,3aS,7aS)-1-{(2S)-2-[(1S)-1-(ethoxycarbonyl)butylamino]-propionyl}octahydro-1H-indole-2-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07358372B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-16be0b7180d344538a908adc42d47ff8 |
| Source note | uspto-grants-2008_04 |