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S. M.H. Al-Majidi & L. H.K Kaka Hama
College of Science, University of Baghdad
DOI: https://doi.org/10.17656/jzs.10360
Abstract:
A series of new 5-BromoIsatin linked to spiro thiazolidinone, Imidazolinone and azetidinone moieties were synthesized. Schiff bases 3-(substituted –imino)-1H-indole-2one(1-5),which were prepared by condensation 5-bromoisatin with different substituted aromatic amine in the presence of glacial acetic acid and Dimethyl- formamide (DMF) as a solvent. Three routs with different reagents were used for the cyclization of the Prepared Schiff bases,the reagents(2-mercaptoaceticacid,2-aminoaceticacid and monochloroacetylchloride) to form spiro-Thiazolidinone(6-10), spiro-imidazolinone (11-15) and spiro-azetidinone (16-20) derivatives respectively. The structures of the newly synthesized compounds were identified by spectral methods FTIR,1H-NMR. Furthermore the effects of the preparing compounds on some strains of bacteria and one yeast were studied.
Keywords:
5-Bromo isatin
Schiff base
Spiro- thiazoildinone
Spiro Imidazolinone Spiro-azetidinone antimicrobial activity.
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