Issue 27, 2014

Facile synthesis of 2-amino-3-bromoquinolines by palladium-catalyzed isocyanide insertion and cyclization of gem-dibromovinylanilines

Abstract

A novel and efficient synthesis of 2-amino-3-bromoquinolines through palladium-catalyzed isocyanide insertion followed by intramolecular cyclization of gem-dibromovinylanilines was developed. The reactions were carried out in 1,4-dioxane at 100 °C for 2–3 h and the corresponding products were obtained in good isolated yields.

Graphical abstract: Facile synthesis of 2-amino-3-bromoquinolines by palladium-catalyzed isocyanide insertion and cyclization of gem-dibromovinylanilines

Supplementary files

Article information

Article type
Communication
Submitted
28 Jan 2014
Accepted
05 Mar 2014
First published
07 Mar 2014

RSC Adv., 2014,4, 13850-13853

Author version available

Facile synthesis of 2-amino-3-bromoquinolines by palladium-catalyzed isocyanide insertion and cyclization of gem-dibromovinylanilines

B. Jiang, L. Hu and W. Gui, RSC Adv., 2014, 4, 13850 DOI: 10.1039/C4RA00821A

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