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Synthesis and Evaluation of the Anxiolytic Activity of Some Phthalimide Derivatives in Mice Model of Anxiety



Hassanzadeh F1, 3 ; Rabbani M2, 3 ; Khodarahmi GA1, 3 ; Moosavi M1
Authors
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Authors Affiliations
  1. 1. Department of Medicinal Chemistry, Isfahan University of Medical Sciences, Isfahan, Iran
  2. 2. Department of Pharmacology, Isfahan Pharmaceutical Sciences Research Center, Iran
  3. 3. Isfahan Pharmaceutical Sciences Research Center, Faculty of Pharmacy, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Iranian Journal of Pharmaceutical Research Published:2012

Abstract

The aim of the present study was to synthesis a series of phthalimides based on our previous works and examine their anxiolytic properties. Using a three steps process, phthalimides were prepared from the corresponding di-methyl phthalate derivatives. Phthalic anhydride was nitrated to produce 3-nitrophthalic acid. Ring closer of either 3-nitrophthalic acid or di-methyl phthalate with urea were carried out in reflux condition. Final compounds were prepared by base catalyzed condensation of 4-methylbenzoyl chloride, benzoyl chloride and benzyl chloride with the resulting imides. From the tested compounds, only N-benzoyl 3-nitro-phthalimide was shown to produce anxiolytic activity by increasing the number of entries and time spent in open arms at 10 mg/kg. © 2012 by School of Pharmacy.