Synthesis of some new mono, bis-indolo[1, 2-c]quinazolines: evaluation of their antimicrobial studies

Journal of the Brazilian Chemical Society

Hu, Anren¹  Kakatiya University, Warangal, India¹  Ravinder, Vadde¹  National Dong Hwa University, Hualien, Taiwan¹  Tzu Chi University, Hualien, Taiwan¹  Reddy, P. Muralidhar¹  Rohini, Rondla¹  Shanker, Kanne¹ 

关键词: indolo[1;    2-c]quinazolines;    synthesis;    antibacterial activity;    antifungal activity;   

DOI  :  10.1590/S0103-50532010000500018

学科分类：化学（综合）

来源: SciELO

【 摘 要 】

A convenient three-step strategy is proposed for the synthesis of mono and bis-indolo[1,2-c] quinazolines from 2-(2-aminophenyl)indole and various aryl aldehydes. The newly synthesized compounds were characterized by elemental analysis, IR, 1H NMR, 13C NMR, and mass spectroscopic investigation. All the derivatives were screened for antibacterial (S. aureus, B. subtilis, S. pyogenes, S. typhimurium, E. coli, K. pneumonia) and antifungal (A. niger, C. albicans, T. viridae) activities by cup plate method. Among the compounds tested, mono- indolo[1,2-c] quinazolines (15-18) exhibited good antibacterial activities while 15 and 18 also showed notable antifungal activity. Especially, 19 and 20 exhibited stronger antibacterial as well as antifungal activity against all tested strains.

【 授权许可】

Unknown