TRANSFORMATIONS OF BENZ-SUBSTITUTED 2-METHYL-4-CHLOROQUINOLINES IN THE PRESENCE OF AMINO ACIDS
DOI:
https://doi.org/10.46991/PYSU:B/2012.46.1.003Keywords:
2-methyl-4-chloroquinoline, aromatic amines, aniline, p-toluidineAbstract
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
How to Cite
Aleksanyan, I.L., and L.P. Hambardzumyan. 2012. “TRANSFORMATIONS OF BENZ-SUBSTITUTED 2-METHYL-4-CHLOROQUINOLINES IN THE PRESENCE OF AMINO ACIDS”. Proceedings of the YSU B: Chemical and Biological Sciences 46 (1 (227):3-7. https://doi.org/10.46991/PYSU:B/2012.46.1.003.
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Chemistry
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