Functionally substituted benzo[<i>c</i>]pyrilium salts. Reactions of 4-carbethoxybenzo[<i>c</i>]pyrilium salts with benzylamine

Authors

  • С. Л. Богза L. M. Litvinenko Institute of Physical Organic and Coal Chemistry, National Academy of Sciences of Ukraine, 340114 Donetsk
  • Ю. А. Николюкин L. M. Litvinenko Institute of Physical Organic and Coal Chemistry, National Academy of Sciences of Ukraine, 340114 Donetsk
  • М. Ю. Зубрицкий L. M. Litvinenko Institute of Physical Organic and Coal Chemistry, National Academy of Sciences of Ukraine, 340114 Donetsk
  • В. И. Дуленко L. M. Litvinenko Institute of Physical Organic and Coal Chemistry, National Academy of Sciences of Ukraine, 340114 Donetsk

Abstract

It was shown that benzo[c]pyrilium salts containing an acceptor group at position 4 react with benzylamine to form intermediate N-benzylisoquinolinium salts which then undergo conversion to 2-benzyl-6-benzylaminoisoquinolinium cations and napthylamines.

How to Cite
Bogza, S. L.; Nikolyukin, Yu. A.; Zubritskii, M. Yu.; Dulenko, V. I. Chem. Heterocycl. Compd. 1995, 31, 372. [Khim. Geterotsikl. Soedin. 1995, 317.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01373541

Downloads

Published

1995-03-25

Issue

No. 3 (1995)

Section

Original Papers