Abstract
A novel, efficient and concise synthesis of chirally pure quinapril hydrochloride is described. The key step is the formation of α-amino amide backbone in one step using Ugi three component reaction. This method allows short access to α-amino amide chain which is a part of many drugs used for treatment of high blood pressure. A large molecular library can be synthesized by changing the components in Ugi reaction.
| Original language | English |
|---|---|
| Pages (from-to) | 48-55 |
| Number of pages | 8 |
| Journal | Synthetic Communications |
| Volume | 50 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 02-01-2020 |
All Science Journal Classification (ASJC) codes
- Organic Chemistry
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