Abstract
Reaction of the moiety 3-nitro phthalic anhydride with p- Phenylene diamine in (40 ml) acetic acid to give compound (p-amino phenyl)-3-nitro phthalimide (A1).Which that react with different aromatic aldehyde in ethanol absolute to give compounds hydrazone (A2-A5), then react this compounds (A2-A5) with chloro acetyl chloride in presence of TEA by using DMF as solvent to obtain 2-azetidinones (A6-A9).The compounds of all the newly synthesized structures were confirmed by and ,IR, 1H NMR as well as melting point. Some of these new structures showed antimicrobial activity (A7-A8) and anti-bacterial activity (A7-A8).Antibacterial activity of some prepared compounds against two types of bacteria: Staphylococcus aureus (Gram positive) and E.coli (Gram negative). Some the compounds showed high inhibition activity against bacteria and two fungi (Candida albicans) and (Candida tropicalis.).
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