Log in

First Bis-Organosilicon Derivatives of Aminothiazoles

  • Published:
Russian Journal of General Chemistry Aims and scope Submit manuscript

Abstract

New organosilicon 2-aminothiazolium polyiodides were first synthesized by the reaction of 2-aminothiazole or 2-aminobenzothiazole with bis(iodomethyl) derivatives of silanes or siloxanes. Structure of the obtained compounds was proved by 1Н, 13С, 29Si NMR and UV spectroscopy methods.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Subscribe and save

Springer+ Basic
EUR 32.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or Ebook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Price includes VAT (Germany)

Instant access to the full article PDF.

Scheme
Scheme
Scheme

Similar content being viewed by others

REFERENCES

  1. Alizadeh, S.R. and Hashemi, S.M., Med. Chem. Res., 2021, vol. 30, p. 771. https://doi.org/10.1007/s00044-020-02686-2

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Shareef, M.A., Devi, G.P., Routhu, S.R., Kumar, C.G., Kamal, A., and Babu, B.N., RSC Med. Chem., 2020, vol. 11, p. 1178. https://doi.org/10.1039/D0MD00188K

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Zhilitskaya, L.V., Shainyan, B.A., and Yarosh, N.O., Molecules, 2021, vol. 26, p. 2190. https://doi.org/10.3390/molecules26082190

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Galochkina, A.V., Bollikanda, R.K., Zarubaev, V.V., Tentler, D.G., Lavrenteva, I.N., Slita, A.V., Chirra, N., and Kantevari, S., Arch. Pharm. Chem. Life Sci., 2019, vol. 352, p. e1800225. https://doi.org/10.1002/ardp.201800225

  5. Sultanova, R.M., Lobov, A.N., Shumadalova, A.V., Meshcheryakova, S.A., Zileeva, Z.R., Khusnutdinova, N.S., Vakhitov, V.A., and Vakhitova, Y.V., Nat. Prod. Res., 2021, vol. 35, p. 1340. https://doi.org/10.1080/14786419.2019.1648459

    Article  CAS  PubMed  Google Scholar 

  6. Bala, R., Kumari, P., Sood, S., Kumar, V., Singh, N., and Singh, K., J. Heterocycl. Chem., 2018, vol. 55, p. 2507. https://doi.org/10.1002/jhet.3282

    Article  CAS  Google Scholar 

  7. Maghraby, M.T.-E., Abou-Ghadir, O.M.F., AbdelMoty, S.G., Ali, A.Y., and Salem, O.I.A., Bioorg. Med. Chem., 2020, vol. 28, p. 7115403. https://doi.org/10.1016/j.bmc.2020.115403

    Article  CAS  Google Scholar 

  8. Sever, B., Altıntop, M.D., Özdemir, A., Tabanca, N., Estep, A.S., Becnel, J.J., and Bloomquist, J.R., Open Chem., 2019, vol. 17, p. 288. https://doi.org/10.1515/chem-2019-0027

    Article  CAS  Google Scholar 

  9. Che, J.-Y., Meng, X.-S., Xu, X.-Y., Jiang, S., Gu, Y.-C., and Shi, D.-Q., J. Heterocycl. Chem., 2016, vol. 53, p. 1494. https://doi.org/10.1002/jhet.2453

    Article  CAS  Google Scholar 

  10. Elshaarawy, R.F.M., Mustafa, F.H.A., Sofy, A.R., Hmed, A.A., and Janiak, C., J. Environ. Chem. Eng., 2019, vol. 7, p. 102800. https://doi.org/10.1016/j.jece.2018.11.044

    Article  CAS  Google Scholar 

  11. Wang, X., Lv, P., Zou, H., Li, Y., Li, X., and Liao, Y., Ind. Eng. Chem. Res., 2016, vol. 55, p. 4911. https://doi.org/10.1021/acs.iecr.5b04630

    Article  CAS  Google Scholar 

  12. Xu, Y., Yang, L., Wang, H., Zhang, Y., Yang, X., Pei, M., and Zhang, G., J. Photochem. Photobiol. (A), 2020, vol. 391, p. 112372. https://doi.org/10.1016/j.jphotochem.2020.112372

    Article  CAS  Google Scholar 

  13. Dorofeev, I.А., Zhilitskaya, L.V., and Yarosh, N.О., Russ. J. Gen. Chem., 2021, vol. 91, p. 2447. https://doi.org/10.1134/S1070363221120136

    Article  CAS  Google Scholar 

  14. Zablotskaya, A., Segal, I., Germane, S., Shestakova, I., Domracheva, I., Nesterova, A., Geronikaki, A., and Lukevics, E., Chem. Heterocycl. Compd., 2002, vol. 38, no. 7, p. 859. https://doi.org/10.1023/A:1020698107686

    Article  CAS  Google Scholar 

  15. Shinnosuke, H., Gen, U., Hidekazu, W., Kosuke, S., Jun, S., Emi, Y., Kyohei, H., and Kenichiro, T., Patent WO Japan 2017099237 A1 20170615, 2017.

  16. Reddel, J.C., Senecal, T.D., Bailey, B.C., Camelio, A.M., Mukhopadhyay, S., and Etienne, J.B., Patent US WO 2020263790 A1 20201230, 2020.

  17. Reiller, P., Mercier-Bion, F., Gimenez, N., Barre, N., and Miserque, F., Radiochim. Acta, 2006, vol. 94, nos. 9–11, p. 739. https://doi.org/10.1524/ract.2006.94.9.739

    Article  CAS  Google Scholar 

  18. PASS Online. http://www.pharmaexpert.ru/PASSOnline/

  19. Yarosh, N.O., Zhilitskaya, L.V., Shagun, L.G., Dorofeev, I.A., Larina, L.I., and Klyba, L.V., Russ. J. Org. Chem., 2016, vol. 52, p. 1223. https://doi.org/10.1134/S1070428016080261

    Article  CAS  Google Scholar 

  20. Yarosh, N.O., Zhilitskaya, L.V., Shagun, L.G., Larina, L.I., and Dorofeev, I.А., Russ. J. Gen. Chem., 2015, vol. 85, p. 2304. https://doi.org/10.1134/S1070363215100151

    Article  CAS  Google Scholar 

Download references

ACKNOWLEDGMENTS

The studies were carried out using the equipment of the Baikal Analytical Center for Collective Use of the Siberian Branch of the Russian Academy of Sciences.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to L. V. Zhilitskaya.

Ethics declarations

No conflict of interest was declared by the authors.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Dorofeev, I.А., Zhilitskaya, L.V. & Yarosh, N.О. First Bis-Organosilicon Derivatives of Aminothiazoles. Russ J Gen Chem 92, 806–810 (2022). https://doi.org/10.1134/S1070363222050097

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S1070363222050097

Keywords:

Navigation