4-HYDROXY-2-QUINOLONES. 202. SYNTHESIS, CHEMICAL AND BIOLOGICAL PROPERTIES OF 4-HYDROXY-6,7-DIMETHOXY-2-OXO-1,2-DIHYDROQUINOLINE-3-CARBOXYLIC ACID ALKYLAMIDES

Authors

  • И. В. Украинец National University of Pharmacy
  • О. В. Бевз National University of Pharmacy
  • Е. В. Моспанова Institute of Chemical Technology East Ukraine Volodymyr Dahl National University
  • Л. В. Савченкова Lugansk State Medicinal University
  • С. И. Янкович Lugansk State Medicinal University

DOI:

https://doi.org/10.1007/1258

Keywords:

4-hydroxy-2-oxo-1, 2-dihydroquinoline-3-carboxamides, amidation, analgesic activity, bromination

Abstract

In continuation of the search for potential analgesics amongst 4-hydroxyquinol-2-one derivatives we have proposed and carried out a preparative method of synthesis of 4-hydroxy-6,7-dimethoxy-2-oxo-1,2-dihydroquinoline-3-carboxylic acid alkylamides. It has been shown that bromination of 4-hydroxy-6,7-dimethoxy-2-oxo-1,2-dihydroquinoline-3-carboxylic acid allylamide using an equivalent of molecular bromine occurs with a conventional addition of the halogen to the allyl double bond and not with halocyclization. The results of the study of the analgesic properties of the compounds prepared are presented.

Authors: I. V. Ukrainets, O. V. Bevz, E. V. Mospanova, L. V. Savchenkova, and S. I. Yankovich.

English translation in Chemistry of Heterocyclic Compounds, 2012, 48 (2), pp 320-326

http://link.springer.com/article/10.1007/s10593-012-0992-4

Published

2013-11-29

Issue

Section

Original Papers