SYNTHESIS OF NEW 4(3H)-QUINAZOLINONE DERIVATIVES OF POTENTIAL ANTIMICROBIAL ACTIVITY | ||
| Bulletin of Pharmaceutical Sciences Assiut University | ||
| Article 7, Volume 30, Issue 2, December 2007, Pages 181-192 PDF (255.48 K) | ||
| Document Type: Original Article | ||
| DOI: 10.21608/bfsa.2007.64183 | ||
| Authors | ||
| Awwad A. Radwan* 1; Salah G. Ali2 | ||
| 1Department of Pharmaceutical Organic Chemistry, Faculty of Pharmacy, Assiut University, Assiut-71527, Egypt | ||
| 2Department of Botany and Microbiology, Faculty of Science, Al-Azhar University, 71524 Assiut, Egypt | ||
| Abstract | ||
| A new series of quinazoline-4(3H)-one derivatives containing hydrazone, thiosemicarbazide, pyrazole moiety and 1,2,4triazolo[4,3-a]quinazolin-5-(4H)-one derivatives, were prepared in order to study the effect of such combinations on the expected antimicrobial activity. Synthesis of target compounds (3-8) has been achieved through an interaction of the starting 2a or 2b with different alkyl or aryl isothiocyanate. Condensation of 2a or 2b with various aromatic aldehydes or ketones afforded the corresponding hydrazones 9-12. 1-(4-Pyridinyl)-1,2-dihydro-4phenyl(allyl)-1,2,4-triazolo[4,3-a]quinazolin-5-(4H)-one deriva tives 13, 14 have been synthesized through reflux of compound 9 or 10 in glacial acetic acid. On the other hand, 1-(3-substituted-3,4dihydro-4-quinazolinon-2-yl)-3-(4-chlorophenyl) pyrazole-4-carbaldehyde 15 or 16 has also been synthesized through interaction of compounds 11 or 12 with Vilsmeier-Haack reagent1. The structures of the new compounds were assigned by spectral and elemental methods of analyses. The synthesized compounds were tested for their in vitro antibacterial and antifungal activities. The tested compounds showed moderate antibacterial activity and weak or no antifungal activity. | ||
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