I.V. Galkinaa*, G.L. Takhautdinovaa, Kh.R. Khayarova, L.M. Yusupovab,
O.I Gnezdilova, A.V. Ilyasovc, V.I. Galkina
aKazan Federal University, Kazan, 420008 Russia
bKazan National Research Technological University, Kazan, 420015 Russia
cTatarstan Academy of Sciences, Kazan, 420111 Russia
E-mail: *vig54@mail.ru
Received July 19, 2017
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Abstract
A simple and efficient procedure for synthesis of nucleophilc aromatic substitution products in benzofurazan cycle on the basis of reactions of substituted anilines with 5-chloro-6-nitrobenzofurazan has been elaborated. The obtained products have a broad spectrum of antibacterial and antimycotic activity. The structure of compounds has been confirmed by IR-, NMR-spectroscopy and also by single-crystal X-ray analysis. Thermal stability of the products has been studied by the combined method of thermogravimetry and differential scanning calorimetry (TG-DSC).
Keywords: substituted anilines, 5-chloro-6-nitrobenzofurazan, nucleophilc aromatic substitution, synthesis, structure, heterocyclic compounds
Acknowledgments. This study was funded by the subsidy allocated to Kazan Federal University as part of the state program for increasing its competitiveness among the world's leading centers of science and education (project no. 4.5888.2017/8.9).
Figure Captions
Fig. 1. The molecular structure of product 3 in crystal.
Fig. 2. The packing of compound 3 molecules in crystal.
Fig. 3. The curve of the combined TG-DSC analysis of product 7.
Fig. 4. The NMR-spectrum of 1Н (CDCl3, 400 MHz).
Fig. 5. The molecular structure of product 7 in crystal.
Fig. 6. The packing of compound 7 molecules in crystal.
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For citation: Galkina I.V., Takhautdinova G.L., Khayarov Kh.R., Yusupova L.M., Gnezdilov O.I., Ilyasov A.V., Galkin V.I. Synthesis, structure, and antimicrobial activity of aminated 5-chloro-6-nitrobenzofurazan with substituted anilines. Uchenye Zapiski Kazanskogo Universiteta. Seriya Estestvennye Nauki, 2017, vol. 159, no. 4, pp. 564–574. (In Russian)
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