TRANSFORMATIONS OF BENZ-SUBSTITUTED 2-METHYL-4-CHLOROQUINOLINES IN THE PRESENCE OF AMINO ACIDS

Authors

  • I.L. Aleksanyan Chair of Organic Chemistry, YSU, Armenia
  • L.P. Hambardzumyan Chair of Organic Chemistry, YSU, Armenia

DOI:

https://doi.org/10.46991/PYSUB.2012.46.1.003

Keywords:

2-methyl-4-chloroquinoline, aromatic amines, aniline, p-toluidine

Abstract

Benz-substituted 2-methyl-4-chloroquinolines in DMF and in the presence of aminoacetic or 3-aminopropionic acids form the mixture of substituted 4-N,N-dimethylamino and 4-hydroxy-2-methylquinolines. It is established, that the last compounds are not formed while using aromatic amines and amino acids, particularly aniline, p-toluidine, antranilic and aminobenzoic acids.

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Published

2012-03-01

Issue

Vol. 46 No. 1 (227) (2012)

Section

Chemistry

License

Copyright (c) 2012 Proceedings of the YSU

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

How to Cite

“TRANSFORMATIONS OF BENZ-SUBSTITUTED 2-METHYL-4-CHLOROQUINOLINES IN THE PRESENCE OF AMINO ACIDS”. 2012. Proceedings of the YSU B: Chemical and Biological Sciences 46 (1 (227): 3-7. https://doi.org/10.46991/PYSUB.2012.46.1.003.