Synthesis 2007(21): 3319-3322  
DOI: 10.1055/s-2007-990821
PAPER
© Georg Thieme Verlag Stuttgart · New York

An Improved Synthesis of Methyl 1,3-Dihydro-2H-pyrrolo[3,4-b]quinoline-2-carboxylate

Rufine Akue-Gedua, Philippe Gautret*a, Jean-Pierre Lelieurb, Benoît Rigo*a
a Groupe de Recherche sur l’Inhibition de la Prolifération Cellulaire, EA 2692, Ecole des Hautes Etudes d’Ingénieur, 13 rue de Toul, 59046 Lille, France
Fax: +33(3)28384804; e-Mail: philippe.gautret@hei.fr; e-Mail: rigo@hei.fr ;
b Laboratoire de Spectrochimie Infrarouge et Raman, CNRS UMR 8516, Ecole des Hautes Etudes d’Ingénieur, 13 rue de Toul, 59046 Lille, France
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Publikationsverlauf

Received 6 July 2007
Publikationsdatum:
10. Oktober 2007 (online)

Abstract

Optimization of an old route leads very easily, in four steps, to methyl 1,3-dihydro-2H-pyrrolo[3,4-b]quinoline-2-carboxylate in 45% yield from commercial starting materials. This procedure can be compared to recently described methods whose yields were only 23-28% and required five to seven steps from advanced intermediates and chromatographic purifications. Moreover, using this method, the title compound can now be obtained in large quantities.

10

The same reaction performed with metallic sodium is less effective.11

22

More than 50 g of compound 1b has been easily synthesized using this method.