Conversions of polyfunctional 3-amino-1(2H)iso quinolines

Autor: Volovenko, Yu. M., Volovnenko, T. A., Babichev, F. S., Shevchenko, T.
Zdroj: Chemistry of Heterocyclic Compounds; April 1994, Vol. 30 Issue: 4 p453-457, 5p
Abstrakt: The acylation of 3-amino-4-cyano-1(2H)isoquinolines with benzoyl chloride leading to the formation of 1,3 oxazino[4,5-clisoquinoline-6-ones has been studied. Previously undescribed 1-aminopyrimido[4,5-cJisoquinolirt 6-ones have been obtained by the reaction of the appopriate 3-amino-](2H)isoginolones with formamide. Nucleophilic replacement has been carried out with 3-amino-1-chloroisoquinoline by the action of sodium hydroxide, primary alcohols, hydrazine hydrate, and various amines. 1,2,4-Triazino[2,3-b]isoginolone has been synthesized by condensing 2,3-diamino-1 (2H)isoquinolone with mesoxalic acid ethyl ester.
Databáze: Supplemental Index