Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10595044 | Bioorganic & Medicinal Chemistry Letters | 2010 | 4 Pages |
Abstract
Two new heterocycles, pyrimido[4,5-c]carbazole and pyrimido[5,4-b]indole, were prepared in three steps from 3-aminocarbazole and 3-aminoindole, respectively. The key Friedel-Crafts intramolecular cyclization was realized under microwave irradiation using montmorillonite K-10 clay as a catalyst. The pyrimido[4,5-c]carbazole derivative shows significant micromolar IC50 against cancer cell lines. Unlike similar carbazole and indolocarbazole compounds, the molecule does not interfere with topoisomerase activity.
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Authors
Julien Debray, Walid Zeghida, Brigitte Baldeyrou, Christine Mahieu, Amélie Lansiaux, Martine Demeunynck,