Synthesis 2002(3): 0320-0322
DOI: 10.1055/s-2002-20043
SHORTPAPER
© Georg Thieme Verlag Stuttgart · New York

Synthesis of Methyl 5- and 6-Nitroindole-2-carboxylates by Nitration of Indoline-2-carboxylic Acid

Sergei N. Lavrenov, Sergei A. Lakatosh, Ludmila N. Lysenkova, Alexander M. Korolev, Maria N. Preobrazhenskaya*
G.F. Gause Institute of New Antibiotics, Russian Academy of Medical Sciences, B. Pirogovskaya 11, Moscow 119992, Russia
Fax: +7(095)2450295; e-Mail: lcta@space.ru;
Further Information

Publication History

Received 6 November 2001
Publication Date:
28 July 2004 (online)

Abstract

Indoline-2-carboxylic acid was transformed into 6-nitroindoline-2-carboxylic acid, the methyl ester of which was easily dehydrogenated by DDQ to methyl 6-nitroindole-2-carboxylate (total yield: 67%). Methyl 5-nitroindole-2-carboxylate was obtained by the nitration of methyl 1-acetylindoline-2-carboxylate acid followed by dehydrogenation with MnO2 in toluene in 40% total yield.