SYNTHESIS OF BENZ-SUBSTITUTED 2-METHYL-3-ALKYL-4-MERCAPTOQUINOLINES

Authors

  • A. A. Avetisyan Chair of Organic Chemistry, YSU, Armenia
  • I. L. Aleksanyan Chair of Organic Chemistry, YSU, Armenia
  • V. H. Durgaryan Chair of Organic Chemistry, YSU, Armenia

DOI:

https://doi.org/10.46991/PYSUB.2008.42.2.089

Keywords:

thiuronium salts, 2-methyl-3-alkyl-4-chloroquinolines, alkaline hydrolysis, 2-methyl-3-alkyl-4-mercaptoquinoline

Abstract

Synthesis of benz-substituted 2-methyl-3-alkyl-4-quinolines thiuronium salts was accomplished by the interaction of 2-methyl-3-alkyl-4-chloroquinolines with thiocarbamide. The alkaline hydrolysis of these compounds results to corresponding 2-methyl-3-alkyl-4-mercaptoquinoline.

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Published

2023-09-22

Issue

Vol. 42 No. 2 (216) (2008)

Section

Chemistry

License

Copyright (c) 2023 Proceedings of the YSU

Creative Commons License

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

How to Cite

“SYNTHESIS OF BENZ-SUBSTITUTED 2-METHYL-3-ALKYL-4-MERCAPTOQUINOLINES”. 2023. Proceedings of the YSU B: Chemical and Biological Sciences 42 (2 (216): 89-93. https://doi.org/10.46991/PYSUB.2008.42.2.089.

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