Aims:
This article describes the controlled synthesis and characterization of azo oxazolone as multifunctional
group in which contain Carbonyl, imine and carbon double bond carbon bond, and their ring opening to azo-benzamide derivative in fast reaction( 5<min>90%).
Objective:
UV, IR, proton-NMR, C13-NMR, Elemental analysis and MS spectrometry all synthesized compounds were
tested for antibacterial and antioxidant activity.
Materials and Methods:
Azo benzamide derivatives were prepared by ring opening of azo oxazolone.
Results and Discussion: Chemically structures of synthesized compounds were characterized upon UV, IR, proton-NMR,
C13-NMR, Elemental analysis and MS spectrometry.
Conclusion:
The oxazolone and benzamide compounds (5a, 5c, 5f, 5h, 5j) screened by diffusion method, the results of tested ciprofloxacin as standard. according to the results the tested compound exhibits more resist to the Escherichia coli than
the Staphylococcus aureus . The highest activity of all compound at 800 µg against both types of bacteria, compound (5c
and 5j) have higher activity (inhibition zone 32mm) than the ciprofloxacin (inhibition zone 28mm) against Escherichia coli.
But compound (5j) in all concentration was in active against Staphylococcus aureus. Compound (5a, 5c, 5f and 5h) have
high activity against E.coli. compound (5c) have low activity in all different concentration.
Others:
Also the product compound tested for its anti-oxidant activity by both DPPH and FRAP method. The result showed
that the some compound have moderate anti-oxidant activity in comparison with ascorbic acid as control typically the compounds bearing OCH3and OCH2CH3 group.