Transition Metal‐Free Regioselective Remote C−H Bond 2,2,2‐Trifluoroethoxylation of 8‐Aminoquinoline Derivatives at the C5 Position
Résumé
The regioselective 2,2,2-trifluoroethoxylation at the C5 position of amides derived from the 8-aminoquinoline has been developed. In the presence of PIDA, an unprecedented and undirected transition metal-free transformation was achieved using the readily available and appealing 2,2,2-trifluoroethanol as the fluorinated source. The selective distal 2,2,2-trifluoroethoxylation of an array of amides was achieved in moderate to good yields (12 examples, up to 61 % yield). This approach provided efficient access to high-value added fluorinated quinoline derivatives, key building blocks for bulk and fine chemical industry.
Domaines
Chimie organiqueOrigine | Fichiers produits par l'(les) auteur(s) |
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