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Synthesis of Substituted Bis-Semicarbazides by Reaction of Hexamethylene Diisocyanate with Hydrazine Derivatives

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Abstract

New bis-semicarbazides were obtained by the reaction of hexamethylene diisocyanate with aliphatic and aromatic acids hydrazides, as well as semicarbazide, thiosemicarbazide, and 4-substituted thiosemicarbazides.

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REFERENCES

  1. Ghorbel, I., Afli, A., Abid, S., Tessier, M., El Gharbi, R., and Fradet, A., J. Macromol. Sci. (A), 2011, vol. 48, no. 6, p. 433. https://doi.org/10.1080/10601325.2011.573317

    Article  CAS  Google Scholar 

  2. Zhang, L., Zhang, C., Zhang, W., Zhang, H., and Hou, Z., J. Biomat. Sci. Polymer Ed., 2019, vol. 30, no. 13, p. 1212. https://doi.org/10.1080/09205063.2019.1625525

    Article  CAS  Google Scholar 

  3. Savelyev, Y., Gonchar, A., Movchan, B., Gornostay, A., Vozianov, S., Rudenko, A., Rozhnova, R., and Travinskaya, T., Mater. Today Proc., 2017, vol. 4, no. 1, p. 87. https://doi.org/10.1016/j.matpr.2017.01.196

    Article  Google Scholar 

  4. Gorbunova, M.A., Shukhardin, D.M., Lesnichaya, V.A., Badamshina, E.R., and Anokhin, D.V., Key Eng. Mater., 2019, vol. 816, p. 187. https://doi.org/10.4028/www.scientific.net/KEM.816.187

    Article  Google Scholar 

  5. Xu, Y. and Xie, D., J. Composite Mater., 2018, vol. 52, no. 12, p. 1579. https://doi.org/10.1177/0021998317729004

    Article  CAS  Google Scholar 

  6. Joseph, J., Patel, R.M., Wenham, A., and Smith, J.R., Int. J. Surface Eng. Coat., 2018, vol. 96, no. 3, p. 121. https://doi.org/10.1080/00202967.2018.1450209

    Article  CAS  Google Scholar 

  7. Kumar, S., Deepak, V., Kumari, M., and Dutta, P.K., Int. J. Biol. Macromol., 2016, vol. 84, p. 349. https://doi.org/10.1016/j.ijbiomac.2015.12.027

    Article  CAS  PubMed  Google Scholar 

  8. Marzec, M., Kucińska-Lipka, J., Kalaszczyńska, I., and Janik, H., Mat. Sci. Eng. (C), 2017, vol. 80, p. 736. https://doi.org/10.1016/j.msec.2017.07.047

    Article  CAS  Google Scholar 

  9. Kinoshita, T., Odavara, S., Fukumura, K., and Furukawa, S., J. Heterocycl. Chem., 1985, vol. 22, p. 1573. https://doi.org/10.1002/jhet.5570220621

    Article  CAS  Google Scholar 

  10. Yang, F., Jiao, Z., Huang, Z., Xie, J., and Gou, H., J. Incl. Phenom. Macrocycl. Chem., 2012, vol. 74, nos. 1–4, p. 257. https://doi.org/10.1007/s10847-012-0108-x

    Article  CAS  Google Scholar 

  11. Guizzardi, R., Vaghi, L., Marelli, M., Natalello, A., Andreosso, I., Papagni, A., and Cipolla, L., Molecules, 2019, vol. 24, no. 3, p. 589. https://doi.org/10.3390/molecules24030589

    Article  CAS  PubMed Central  Google Scholar 

  12. Read, G. and Richardson, R.R., J. Chem. Soc. Perkin Trans. 1, 1996, no. 2, p. 167. https://doi.org/10.1039/P19960000167

    Article  Google Scholar 

  13. Shevchenko, V.V., Klimenko, N.S. and Vasilevskaya, G.A., Zh. Org. Khim., 1982, vol. 18, no. 12, p. 2547.

    CAS  Google Scholar 

  14. Pitucha, M., Chodkowska, A., Maciejewski, M., Jagiello-Wójtowicz, E., and Pachuta-Stec, A., Monatsh. Chem., 2010, vol. 141, p. 199. https://doi.org/10.1007/s00706-009-0242-3

    Article  CAS  Google Scholar 

  15. Ceylan, Ş., Cebeci, Y.U., Demirbaş, N., Batur, Ö.Ö., and Özakpınar, Ö.B., Chem. Select., 2020, vol. 5, no. 36, p. 11340. https://doi.org/10.1002/slct.202002779

    Article  CAS  Google Scholar 

  16. Pitucha, M., Borowski, P., Karczmarzyk, Z., and Fruziński, A., J. Mol. Struct., 2009, vol. 919, nos. 1–3, p. 170. https://doi.org/10.1016/j.molstruc.2008.09.002

    Article  CAS  Google Scholar 

  17. Pitucha, M., Rzymowska, J., Olender, A., and Grzybowska-Szatkowska, L., J. Serb. Chem. Soc., 2012, vol. 77, no. 1, p. 1. https://doi.org/10.2298/JSC110212157P

    Article  CAS  Google Scholar 

  18. Javaid, M.A., Zia, K.M., Khera, R.A., Jabeen, S., Mumtaz, I., Younis, M.A., Shoaib, M., and Bhatti, I.A., Int. J. Biol. Macromol., 2019, vol. 129, p. 116. https://doi.org/10.1016/j.ijbiomac.2019.01.084

    Article  CAS  PubMed  Google Scholar 

  19. Wisnewski, A.V., Liu, J., and Nassar, A.F., Xenobiotica, 2016, vol. 46, no. 8, p. 726. https://doi.org/10.3109/00498254.2015.1118576

    Article  CAS  PubMed  Google Scholar 

  20. Zhang, J., Sun, X., Chen, Y., Mi, Y., Tan, W., Miao, Q., Li, Q., Dong, F., and Guo, Z., Carbohydrate Polym., 2020, vol. 234, p. 115903. https://doi.org/10.1016/j.carbpol.2020.115903

    Article  CAS  Google Scholar 

  21. Burmistrov, V.V., D’yachenko, V.S., Rasskazova, E.V., and Butov, G.M., Russ. J. Org. Chem., 2019, vol. 55, no. 8, p. 1166. https://doi.org/10.1134/S1070428019080165

    Article  CAS  Google Scholar 

  22. Butov, G.M., Burmistrov, V.V., Dalinger, I.L., Vatsadze, I.A., Shkineva, T.K., and Danilov, D.V., Chem. Heterocycl. Compd., 2015, vol. 50, no. 12. https://doi.org/10.1007/s10593-015-1643-3

  23. Haces, A., Breitman, T.R., and Driscoll, J.S., J. Med. Chem., 1987, vol. 30, no. 2, p. 405. https://doi.org/10.1021/jm00385a025

    Article  CAS  PubMed  Google Scholar 

  24. Pitucha, M. and Nowak, R., Lett. Drug Design Discov., 2011, vol. 8, no. 10, p. 1004. https://doi.org/10.2174/157018011797655188

    Article  CAS  Google Scholar 

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Funding

The work was carried out within the framework of the basic part of the governmental task of the Ministry of Science and Higher Education (no. 785.00.X6019) using the equipment of the Engineering Center of the St. Petersburg State Institute of Technology (Technical University).

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Authors and Affiliations

  1. St. Petersburg State Institute of Technology (Technical University), 190013, St. Petersburg, Russia

    A. S. Skrylkova & D. M. Egorov

  2. JSC GK “Khimik”, 190013, St. Petersburg, Russia

    R. V. Tarabanov

Authors
  1. A. S. Skrylkova
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  2. D. M. Egorov
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  3. R. V. Tarabanov
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Corresponding author

Correspondence to D. M. Egorov.

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No conflict of interest was declared by the authors.

Additional information

Translated from Zhurnal Obshchei Khimii, 2021, Vol. 91, No. 10, pp. 1627–1631 https://doi.org/10.31857/S0044460X21100206.

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Skrylkova, A.S., Egorov, D.M. & Tarabanov, R.V. Synthesis of Substituted Bis-Semicarbazides by Reaction of Hexamethylene Diisocyanate with Hydrazine Derivatives. Russ J Gen Chem 91, 2110–2113 (2021). https://doi.org/10.1134/S1070363221100200

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  • DOI: https://doi.org/10.1134/S1070363221100200

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