Metal-Free Coupling of Azoles with 2- and 3-Haloindoles Providing Access to Novel 2- or 3-(Azol-1-yl)indole Derivatives

Thermal or microwave-mediated heating of 2- or 3-haloindoles with azoles (pK a < 8) provides a straightforward, metal-free, and environmentally friendly access to novel 2-(azol-1-yl)indoles. Furthermore, previously unknown 2,3-bis(azolyl-1-yl)indoles can be prepared from 2,3-dihaloindoles by sequ...

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Veröffentlicht in:Organic letters 2010-05, Vol.12 (10), p.2334-2337
Hauptverfasser: Poirier, Martin, Goudreau, Sébastien, Poulin, Jason, Savoie, Jolaine, Beaulieu, Pierre L
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Sprache:eng
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Zusammenfassung:Thermal or microwave-mediated heating of 2- or 3-haloindoles with azoles (pK a < 8) provides a straightforward, metal-free, and environmentally friendly access to novel 2-(azol-1-yl)indoles. Furthermore, previously unknown 2,3-bis(azolyl-1-yl)indoles can be prepared from 2,3-dihaloindoles by sequential reaction with two distinct azoles. This operationally simple acid-catalyzed process delivers novel indole derivatives in fair to excellent yields and expands the chemical diversity of substitutions that can be introduced on this medicinally important scaffold.
ISSN:1523-7060
1523-7052
DOI:10.1021/ol100685p