Abstract
The mixed azines 3a-h and 4 were obtained by treating 3-hydrazonoindolin-2-one (2) with the appropriate aldehyde or dialdehyde. Treatment of 3b or 3c with formaldehyde or glutaric dialdehyde and the appropriate amine afforded the azine Mannich bases 5-7. The condensation of isatin or its N-Mannich base 8 with 1-aminopiperidine, 4-aminomorpholine and 1,4-diaminopiperazine gave 10a- d, 12 and 13. The Mannich bases 14 and 15 were obtained from 10a and 10b. Treatment of 2 with succinic, phthalic and quinolinic anhydride and pyromellitic dianhydride afforded compounds 16, 17a, 17b and 18, respectively. The synthesis of isatin Schiff bases incorporating a benzoylpiperidine, benzoylmorpholine and 1,4-dibezoylpiperazine moiety and their N-Mannich bases was investigated.
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Afsah, E. M., Elmorsy, S. S., Abdelmageed, S. M., & Zaki, Z. E. (2015). Synthesis of some new mixed azines, Schiff and Mannich bases of pharmaceutical interest related to isatin. Zeitschrift Fur Naturforschung - Section B Journal of Chemical Sciences, 70(6), 393–402. https://doi.org/10.1515/znb-2014-0262
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