Challenges and Advances in Chemical Science Vol. 1

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Exploration of Newer Possibilities to the Synthesis of Diazepine and Quinoline Carboxylic Acid Substituted Analogues of Benzothiazolo Condensed Oxocarbazoles and Oxoazacarbazoles of Medicinal Interest

  • Vatsala Soni
  • Meenakshi Sharma
  • Vaishali Soni
  • Shiv Lal Soni

Challenges and Advances in Chemical Science Vol. 1, 14 June 2021 , Page 43-53
https://doi.org/10.9734/bpi/cacs/v1/2264F Published: 2021-06-14

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Abstract

Heterocyclic systems containing benzothiazoles, carbazole (and azacarbazole) moieties have attracted the attention of chemists owing to these nuclei having been identified in the literature as most promising pharmacophores in drug design and synthesis. Based on these observations, it could be anticipated that incorporation of the bioactive azepine moiety and quinoline moiety into the molecular framework of benzothiazoles fused to carbazole (and azacarbazoles) could produce interesting series of compounds 9-12 with enhanced biological activities, whose structure was unequivocally established from its micro analyses and spectral data.

Keywords:
  • Benzothiazole
  • carbazole
  • azacarbazole
  • pfitzinger reaction
  • beckmann rearrangement

How to Cite

Soni, V. ., Sharma, M. ., Soni, V. ., & Soni, S. L. . (2021). Exploration of Newer Possibilities to the Synthesis of Diazepine and Quinoline Carboxylic Acid Substituted Analogues of Benzothiazolo Condensed Oxocarbazoles and Oxoazacarbazoles of Medicinal Interest . Challenges and Advances in Chemical Science Vol. 1, 43–53. https://doi.org/10.9734/bpi/cacs/v1/2264F
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