STUDY OF LACTAMS. VI. SYNTHESIS OF 6-SUBSTITUTED PURINO[8,9-1<sup>1</sup>,2<sup>2</sup>]ISOINDOLINES

Authors

  • P. Г. Глушков Ordzhonikidze All-Union Chemical-Pharmaceutical Scientific Research Institute, Moscow
  • O. Ю. Магидсон Ordzhonikidze All-Union Chemical-Pharmaceutical Scientific Research Institute, Moscow

DOI:

https://doi.org/10.1007/145

Abstract

It is shown with 1-ethoxyisoindolenine that the reaction of lactim ethers with α-amino-α-cyanoacetamide also extends to partly aromatized lactim ethers, although these react much less readily. Condensation of 1-ethoxyisoindolenine with α-amino-cyanoacetamide gives 4-carbamido-5-aminoimidazo[1, 2-1′, 2′]isoindoline, from which a new series of purinoisoindioline derivatives is synthesized.

Authors: R. G. Glushkov, O. Yu. Magidson.

English Translation in Chemistry of Heterocyclic Compounds, 1965, 1 (1), pp 57-59

http://link.springer.com/article/10.1007/BF01168921

Published

2013-01-09

Issue

Section

Original Papers