Synthesis of some new anils: part 1. Reaction of 2-hydroxy-benzaldehyde and 2-hydroxynaphthaldehyde with 2-aminopyridene and 2-aminopyrazine |
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| Authors: | Asiri Abdullah M Badahdah Khadija O |
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| Affiliation: | Chemistry Department, Faculty of Science, King Abdul Aziz University, Jeddah 21413, P. O. Box 80203, Saudi Arabia. aasiri2@kaau.edu.sa |
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| Abstract: | New Schiff bases derived from 2-aminopyridene and 2-aminopyrazine have been synthesized. The UV-Visible spectra of the compounds have been investigated in acetonitrile and toluene. The compounds were in tautomeric equilibrium (enol-imine O- H...N, keto-amine O...H-N forms) in polar and nonpolar solvents. For some derivatives the keto-amine form was observed in both toluene and acetonitrile. 1H-NMR and IR results showed that all Schiff bases studied favor the enol-imine form over the keto form in a weakly polar solvent such as deuterochloroform. |
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