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
DOI:
https://doi.org/10.1007/309Keywords:
anthranilic acid, 4(3H)-benzoxazinones, 2H-1-benzopyrans, 2-iminocoumarins, 4(3H)-quinazolinones, recyclizationAbstract
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