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

Authors

  • Vatsala Soni Department of Chemistry, Banasthali University, Banasthali, 304022, Rajasthan, India.
  • Meenakshi Sharma Department of Chemistry, Banasthali University, Banasthali, 304022, Rajasthan, India.
  • Vaishali Soni SKRAU, Bikaner, Raj, 334001, India.
  • Shiv Lal Soni PGIMER, Chandigarh, 160012, India.

DOI:

https://doi.org/10.9734/bpi/cacs/v1/2264F

Keywords:

Benzothiazole, carbazole, azacarbazole, pfitzinger reaction, beckmann rearrangement

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.

Published

2021-06-14

How to Cite

Vatsala Soni, Meenakshi Sharma, Vaishali Soni, & Shiv Lal Soni. (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