Abstract
A simple and practical synthetic approach for tasigna was described here in six steps with high yield (40β). All of the intermediates and final target compound were isolated cleanly in high yield without a need for chromatographic purification. Significantly, the facile synthetic route proposed in this work has the characteristics of mild synthetic conditions, inexpensive reagents, high yield and simple operation.
| Original language | English |
|---|---|
| Pages (from-to) | 985-989 |
| Number of pages | 5 |
| Journal | Medicinal Chemistry |
| Volume | 8 |
| Issue number | 5 |
| DOIs | |
| State | Published - Sep 2012 |
Keywords
- Bcr-Abl kinase inhibitor
- Condensation
- Cu-catalyzed N-arylation
- Facile synthesis
- Tasigna
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