| Acceptance rate | 46% |
|---|---|
| Time to first decision | 6 months* |
| Time to decision with review | 50 days* |
*Approximate number of days
**The days mentioned above are averages and do not indicate exact durations. The process may vary for each article.
ACTA Pharmaceutica Sciencia
2020 , Vol 58 , Num 1
Synthesis and Investigations of Antimicrobial, Antioxidant Activities of Novel Di-[2-(3-alkyl/ aryl-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl)- azomethinephenyl] Isophtalates and Mannich Base Derivatives
1 Kafkas University, Department of Chemistry, Chemistry, Kars, Turkey2 Kafkas University, Kars Vocational School, Chemistry, Kars, Turkey
3 Kafkas University, Faculty of Education, Mathematics and Science Education, Kars, Turkey
DOI : 10.23893/1307-2080.APS.05804 Viewed : 15692 - Downloaded : 4827 In this study, the synthesis of di-[2-(3-alkyl/aryl-4,5-dihydro-1H-1,2,4-triazol- 5-one-4-yl)-azomethinephenyl] isophtalates (2a-g) from the reactions of 3-alkyl/ aryl-4-amino-4,5-dihydro-1H-1,2,4-triazol-5-ones (1a-g) with di-(2-formylphenyl) isophtalate is described. Then, the compounds 2 were treated with morpholine in the presence of formaldehyde to synthesize di-{2-[1-(morpholine-4-yl-methyl)-3- alkyl(aryl)-4,5-dihydro-1H-1,2,4-triazol-5-one-4-yl]-azomethinephenyl} isophtalates (3a-g). The newly synthesized compounds were characterized using IR, 1HNMR and 13C-NMR spectral data. In addition, the compounds synthesized were screened for their antimicrobial activities. Furthermore, the antioxidant properties of the newly synthesized compounds were analysed for their in-vitro potential antioxidant activities in three different methods (reducing power, free radical scavenging and metal chelating activity). These antioxidant activities were compared to those from standard antioxidants, such as BHA, BHT, EDTA and ?-tocopherol. Keywords : Schiff base, Mannich base, Antimicrobial activity, Antioxidant activity