Synthesis 1992; 1992(10): 969-972
DOI: 10.1055/s-1992-26281
paper
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Oxokohlenstoffe und verwandte Verbindungen;18. Mitteilung1. Umsetzung von Perchlorcyclobutenon mit Pyridinen: Synthese von 4H-4-Chinolizinonen im Eintopfverfahren

Arthur H. Schmidt* , Mario Dümmler
  • *Abteilung für Organische Chemie und Biochemie, Fachhochschule Fresenius, Kapellenstraße 11-15, D-6200 Wiesbaden, Germany
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
17. September 2002 (online)

Oxocarbons and Related Compounds; Part 18.1 The Reaction of Perchlorocyclobutenone with Pyridines: A Novel Synthesis of 4H-4-Quinolizinones Heating of tetrachlorocyclobutenone (5) with the pyridines 6a-i followed by treatment with water affords 1,3-dichloro-2-hydroxy-4H-4-quinolizinones 7a, b, g-h and 1,3-dichloro-2-hydroxy-4-oxo-4H-quinolizinecarboxylates 7c-f. The reaction pathway has been secured by trapping 1,2,3-trichloro-8-(1,1-dimethylethyl)-4H-4-quinolizinone (11b) and by its successive conversion to 7b on heating with water.