Synthesis and Spectroscopic Study of Some New 1,2,4-Triazino[5,6-b]indole Derivatives

Authors

  • Abdulkarim H. Al-Syari Chemistry Department, Faculty of Science, Sana`'a University, Sana'a, Yemen
  • Saieba S. Hassan Chemistry Department, Faculty of Science, Sana'a University, Sana'a, Yemen
  • Zeina Al-dulaimy Chemistry Department, Faculty of Science, Sana'a University, Sana'a, Yemen

DOI:

https://doi.org/10.59167/tujnas.v2i2.1274

Keywords:

Isatin, 5-bromo isatin, synthesis, derivatives & characterization

Abstract

The Scheme of this work included the synthesis and characterization of new two series of 1,2,4-triazino[5,6-b] indole and 8-bromo-1,2,4-triazino[5,6-b] indole derivatives according to the starting material used. Both, derivatives of 3-thione-1,2,4-triazino[5,6-b] indole and 8-bromo-3-thione-1,2,4-triazino[5,6-b] indole (3a & 3b) were prepared by using Isatin and 5-bromo isatin as a starting material, the new schiff`s bases (5a & 5b) were synthesized by the reaction of hydrazino indole derivatives (4a & 4b) with aromatic aldehydes. Tetracyclic derivatives (7a & 7b) were prepared by the reaction of hydrazino derivatives (4a & 4b) with carbon disulfide in the presence of pyridine. Also 3-(N-phenyl thiocarbamoyl hydrazino)-1,2,4-triazino-[5,6-b] indole, and 8-bromo-3-(N phenyl thiocarbamoyl hydrazino)-1,2,4-triazino-[5,6-b] indole (6a & 6b) were prepared by the reaction of the compound (4a & 4b) with phenyl thio isocyanate in the presence of DMF. Finally, new Mannich bases (9a & 9b) were prepared by the reaction of the new acetylenic indole derivatives (8a & 8b) with paraformaldehyde and secondary amine in the presence of coprous chloride as catalyst. These compounds were identified by their melting points and spectral data (IR & UV), and elemental analysis (C,H,N) and thin layer chromatography (TLC) were used.

Published

27-01-2023

How to Cite

Al-Syari, A. H., Hassan , S. S., & Al-dulaimy, Z. (2023). Synthesis and Spectroscopic Study of Some New 1,2,4-Triazino[5,6-b]indole Derivatives. Thamar University Journal of Natural & Applied Sciences, 2(1), 57–68. https://doi.org/10.59167/tujnas.v2i2.1274

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