Solid-phase bromination and Suzuki coupling of 2-carboxyindoles.

Comb Chem High Throughput Screen

Division of Pharmaceutical Chemistry, Department of Pharmacy, University of Helsinki, P. O. Box 56, FIN-00014 Helsinki, Finland.

Published: September 2001

As part of an ongoing lead discovery project we have developed a convenient method for the modification and substitution of indole moieties at the 3-position. Selective bromination of three different 2-carboxyindoles was followed by Suzuki cross-coupling with aryl and heteroaryl boronic acids on a Merrifield resin solid-phase. After column chromatography, yields of the 3- substituted indoles ranged from 42-98%.

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http://dx.doi.org/10.2174/1386207013330887DOI Listing

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