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Modification of phenothiazine and carbazole derivatives with trifluoromethyl-containing 1,3,5-oxadiazines and imidazolidinediones

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Abstract

Modification of phenothiazine and carbazole derivatives with trifluoromethyl-containing 1,3,5-oxadiazines and imidazolidinediones based on the copper(I)-catalyzed alkyne-azide 1,3-cycloaddition was carried out.

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References

  1. A. Gluszynska, Eur. J. Med. Chem., 2015, 94, 405; DOI: https://doi.org/10.1016/j.ejmech.2015.02.059.

    Article  CAS  Google Scholar 

  2. A. D. Mosnaim, V. V. Ranade, M. E. Wolf, J. Puente, M. A. Valenzuela, Am. J. Ther., 2006, 13, 261; DOI: https://doi.org/10.1097/01.mjt.0000212897.20458.63.

    Article  Google Scholar 

  3. K. Pluta, B. Morak-Młodawska, M. Jelen, Eur. J. Med. Chem., 2011, 46, 3179; DOI: https://doi.org/10.1016/j.ejmech.2011.05.013.

    Article  CAS  Google Scholar 

  4. R. G. Zenkov, L. V. Ektova, O. A. Vlasova, G. A. Belitskiy, M. G. Yakubovskaya, K. I. Kirsanov, Chem. Heterocycl. Compd. (Engl. Transl.), 2020, 56, 644; DOI: https://doi.org/10.1007/s10593-020-02714-4.

    Article  CAS  Google Scholar 

  5. W. Murray, D. C. Rees, Nat. Chem., 2009, 1, 187; DOI: https://doi.org/10.1038/nchem.217.

    Article  CAS  Google Scholar 

  6. M. G. Savelieff, G. Nam, J. Kang, H. J. Lee, M. Lee, M. H. Lim, Chem. Rev., 2019, 119, 1221; DOI: https://doi.org/10.1021/acs.chemrev.8b00138.

    Article  CAS  Google Scholar 

  7. S. O. Bachurin, E. F. Shevtsova, G. F. Makhaeva, V. V. Grigoriev, N. P. Boltneva, N. V. Kovaleva, S. V. Lushchekina, P. N. Shevtsov, M. E. Neganova, O. M. Redkozubova, E. V. Bovina, A. V. Gabrelyan, V. P. Fisenko, V. B. Sokolov, A. Yu. Aksinenko, V. Echeverria, G. E. Barreto, G. Aliev, Sci. Rep., 2017, 45627; DOI: https://doi.org/10.1038/srep45627.

  8. G. F. Makhaeva, S. V. Lushchekina, N. P. Boltneva, V. B. Sokolov, V. V. Grigoriev, O. G. Serebryakova, E. A. Vikhareva, A. Yu. Aksinenko, G. E. Barreto, G. Aliev, S. O. Bachurin, Sci. Rep., 2015, 13164; DOI: https://doi.org/10.1038/srep13164.

  9. V. B. Sokolov, G. F. Makhaeva, A. Yu. Aksinenko, V. V. Grigoriev, E. F. Shevtsova, S. O. Bachurin, Russ. Chem. Bull., 2017, 66, 1821; DOI: https://doi.org/10.1007/s11172-017-1953-y.

    Article  CAS  Google Scholar 

  10. S. O. Bachurin, E. P. Shevtsova, N. N. Lermontova, T. P. Serkova, R. R. Ramsay, Neurotoxicology, 1996, 17, 897.

    CAS  PubMed  Google Scholar 

  11. G. F. Makhaeva, E. F. Shevtsova, N. V. Kovaleva, E. V. Rudakova, M. E. Neganova, L. G. Dubova, P. N. Shevtsov, A. Yu. Aksinenko, V. B. Sokolov, S. O. Bachurin, Russ. Chem. Bull., 2018, 67, 2121; DOI: https://doi.org/10.1007/s11172-018-2338-6.

    Article  CAS  Google Scholar 

  12. V. B. Sokolov, A. Yu. Aksinenko, T. V. Goreva, T. A. Epishina, S. O. Bachurin, Russ. Chem. Bull., 2019, 68, 2241; DOI: https://doi.org/10.1007/s11172-019-2693-y.

    Article  CAS  Google Scholar 

  13. A. Yu. Aksinenko, T. V. Goreva, T. A. Epishina, Russ. Chem. Bull., 2021, 70, 487; DOI: https://doi.org/10.1007/s11172-021-3113-7.

    Article  CAS  Google Scholar 

  14. X. Cao, S. Ke, Rec. Adv. Med. Chem., 2015, 2, 107; DOI: https://doi.org/10.2174/97816810817171150201.

    Google Scholar 

  15. L. Konnert, F. Lamaty, J. Martinez, E. Colacino, Chem. Rev., 2017, 117, 13757; DOI: https://doi.org/10.1021/acs.chemrev.7b00067.

    Article  CAS  Google Scholar 

  16. V. B. Sokolov, A. Yu. Aksinenko, Russ. Chem. Bull., 2013, 61, 2124; DOI: https://doi.org/10.1007/s11172-012-0297-x.

    Article  Google Scholar 

  17. V. B. Sokolov, A. Yu. Aksinenko, A. V. Sokolov, A. V. Gabrelian, A. D. Efimova, V. V. Grigoriev, Russ. Chem. Bull., 2017, 66, 99; DOI: https://doi.org/10.1007/s11172-017-1706-y.

    Article  CAS  Google Scholar 

  18. S. Bachurin, S. Tkachenko, I. Baskin, N. Lermontova, T. Mukhina, L. Petrova, A. Ustinov, A. Proshin, V. Grigoriev, N. Lukoyanov, V. Palyulin, N. Zefirov, Ann. N.-Y. Acad. Sci., 2001, 939, 219; DOI: https://doi.org/10.1111/j.1749-6632.2001.tb03629.x.

    Article  CAS  Google Scholar 

  19. S. O. Bachurin, S. I. Gavrilova, A. Samsonova, G. E. Barreto, G. Aliev, Pharmacol. Res., 2018, 129, 216; DOI: https://doi.org/10.1016/j.phrs.2017.11.021.

    Article  CAS  Google Scholar 

  20. A. Yu. Aksinenko, T. V. Goreva, T. A. Epishina, A. N. Pushin, V. B. Sokolov, Russ. Chem. Bull., 2006, 55, 1052; DOI: https://doi.org/10.1007/s11172-006-0375-z.

    Article  CAS  Google Scholar 

  21. V. B. Sokolov, A. Yu. Aksinenko, T. A. Epishina, T. V. Goreva, I. V. Martynov, Russ. Chem. Bull., 2005, 54, 2851; DOI: https://doi.org/10.1007/s11172-006-0200-8.

    Article  CAS  Google Scholar 

  22. C. Sae-Lim, D. J. Sandman, B. M. Foxman, M. Sukwat-tanasinitt, J. Macromol. Sci. (A), 2006, 43, 1929; DOI: https://doi.org/10.1080/10601320600996114.

    Article  CAS  Google Scholar 

  23. K. Kolli, B. Prasad, P. V. Babu, M. A. Ashfaq, N. Z. Ehtesham, R. R. Raju, M. Pal, Org. Biomol. Chem., 2014, 12, 6080; DOI: https://doi.org/10.1039/c4ob00686k.

    Article  CAS  Google Scholar 

  24. V. B. Sokolov, A. Yu. Aksinenko, T. A. Epishina, T. V. Goreva, Russ. Chem. Bull., 2018, 67, 1679; DOI: https://doi.org/10.1007/s11172-018-2276-3.

    Article  CAS  Google Scholar 

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Funding

This work was financially supported by the Russian Science Foundation (Project No. 19-13-00378). The research was carried out using equipment of the Center for Collective use of the Institute of Physiologically Active Compounds of the Russian Academy of Sciences.

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Authors and Affiliations

  1. Institute of Physiologically Active Compounds, Russian Academy of Sciences, 1 Severnyi proezd, 142432, Chernogolovka, Moscow Region, Russian Federation

    A. Yu. Aksinenko, V. B. Sokolov, A. V. Gabrel’yan, V. V. Grigoriev & S. O. Bachurin

Authors
  1. A. Yu. Aksinenko
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  2. V. B. Sokolov
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  3. A. V. Gabrel’yan
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  4. V. V. Grigoriev
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  5. S. O. Bachurin
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Corresponding author

Correspondence to A. Yu. Aksinenko.

Additional information

Dedicated to Academician of the Russian Academy of Sciences O. M. Nefedov on the occasion of his 90th birthday.

Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2180–2184, November, 2021.

This paper does not contain descriptions of studies on animals or humans.

The authors declare no competing interests.

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Aksinenko, A.Y., Sokolov, V.B., Gabrel’yan, A.V. et al. Modification of phenothiazine and carbazole derivatives with trifluoromethyl-containing 1,3,5-oxadiazines and imidazolidinediones. Russ Chem Bull 70, 2180–2184 (2021). https://doi.org/10.1007/s11172-021-3329-6

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  • DOI: https://doi.org/10.1007/s11172-021-3329-6

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