RECYCLIZATION OF 2-IMINO-2H-1-BENZOPYRANS UNDER THE ACTION OF NUCLEOPHILIC REAGENTS. 5. INTERACTION OF 2-IMINOCOUMARIN-3-CARBOXAMIDE WITH ANTHRANILIC ACID AND ITS DERIVATIVES

Authors

  • С. Н. Коваленко Ukrainian Pharmaceutical Academy
  • И. Е. Былов Ukrainian Pharmaceutical Academy
  • Я. В. Белоконь Ukrainian Pharmaceutical Academy
  • В. П. Черных Ukrainian Pharmaceutical Academy

DOI:

https://doi.org/10.1007/309

Keywords:

anthranilic acid, 4(3H)-benzoxazinones, 2H-1-benzopyrans, 2-iminocoumarins, 4(3H)-quinazolinones, recyclization

Abstract

N-Substituted 2-iminocoumarins are formed on reacting 2-iminocoumarin-3-carboxamide with anthranilic acid, methyl anthranilate, anthranilamide, and anthranilonotrile. Depending on the reaction conditions these recyclize into the corresponding 3-substituted coumarins or are hydrolyzed to coumarin-3-carboxamide. An alternative synthesis of some of the compounds has been effected.

Authors: S. N. Kovalenko, I. E. Bylov, Ya. V. Belokon', and V. P. Chernykh.

English Translation in Chemistry of Heterocyclic Compounds, 2000, 36 (9), pp 1026-1031

http://link.springer.com/article/10.1023/A%3A1002773613250

Published

2013-02-13

Issue

Section

Original Papers