Substituted Ureas and Their Analogues Containing Framework Fragments. II. 1,1'-(4-(Adamantan-1-yl)-1,2-phenylene)bis(3-(R-phenylureas)) and Thioureas

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Abstract

The article presents a method for obtaining adamantlyl-containing 1,3-disubstituted diureas and dithioureas containing a 4-(adamantan-1-yl)-1,2-phenylene fragment. The target compounds were synthesized by the reaction of 4-(adamantan-1-yl)benzene-1,2-diamine with aromatic isocyanates and isothiocyanates with yields of 66–93%. It was found that, for the reaction to proceed to high conversion degrees in 12 h, no addition of a base (Et3N) to the reaction mass is required. The proposed approach allows simplifying the synthesis, isolation and purification of the reported compounds.

About the authors

D. M Zapravdina

Volgograd State Technical University (VSTU)

Volgograd, Russia

E. A Eshtukova-Scheglova

MIREA – Russian Technological University

Moscow, Russia

E. V Yakovleva

Volgograd State Technical University (VSTU)

Volgograd, Russia

I. E Nazarov

Volgograd State Technical University (VSTU)

Volgograd, Russia

E. S Ilyina

Volgograd State Technical University (VSTU)

Volgograd, Russia

E. N Savelyev

Volgograd State Technical University (VSTU)

Volgograd, Russia

V. V Burmistrov

Volgograd State Technical University (VSTU)

Email: vburmistrov@vstu.ru
Volgograd, Russia

References

  1. Danilov D.V., D’yachen-ko V.S., Zapravdina D.M., Ilyina E.S., Degtyarenko E.K., Burmistrov V.V. Russ. J. Org. Chem. 2024, 60, 2108–2116. doi: 10.1134/S1070428024110034
  2. Hwang S.H., Wagner K.M., Morisseau C., Liu J.Y., Dong H., Wecksler A.T., Hammock B.D., J. Med. Chem. 2011, 54, 3037–3050. doi: 10.1021/jm2001376
  3. Sun C.P., Zhang X.Y., Morisseau C., Hwang S.H., Zhang Z.J., Hammock B.D., Ma X.C., J. Med. Chem. 2020, 64, 184–215. doi: 10.1021/acs.jmedchem.0c01507
  4. Burmistrov V., Morisseau C., Babkov D.A., Golubeva T., Pitushkin D., Sokolova E.V., Vasipov V., Kuznetsov Ya., Bazhenov S.V., Novoyatlova U.S., Bondarev N.A., Manukhov I.V., Osipova V., Berberova N., Spasov A.A., Butov G.M., Hammock B.D. Int. J. Mol. Sci. 2022, 23, 10710. doi: 10.3390/ijms231810710
  5. Turnbull J., Chapman V. Curr. Opin. Pharm. 2024, 78, 102477. doi: 10.1016/j.coph.2024.102477
  6. Hammock B.D., McReynolds C.B., Wagner K., Buckpitt A., Cortes-Puch I., Croston G., Lee K.S.S., Yang J., Schmidt W.K., Hwang S.H. J. Med. Chem. 2021, 64, 1856–1872. doi: 10.1021/acs.jmedchem.0c01886
  7. Babkov D., Eliseeva N., Adzhienko K., Bagmetova V., Danilov D., McReynolds C.B., Morisseau C., Hammock B.D., Burmistrov V. Int. J. Mol. Sci. 2024, 25, 8841. doi: 10.3390/ijms25168841
  8. Burmistrov V.V., Morisseau C., Danilov D.V., Gladkikh B.P., D’yachenko V.S., Zefirov N.A., Zefirova O.N., Butov G.M., Hammock B.D. J. Enzyme Inhibit. Med. Chem. 2023, 38, 2274797. doi: 10.1080/14756366.2023.2274797
  9. Ding J., Zhu M.-Z., Liu S.-M., Liu R.-C., Xu S., Shehzadi K., Ma H.-L., Yu M.-J., Zhu X.-H., Liang J-H. J. Med. Chem. 2024, 67, 18412–18447. doi: 10.3390/ijms25010338
  10. Griñán-Ferré C., Jarné-Ferrer J., Bellver-Sanchís A., Codony S., Puigoriol-Illamola D., Sanfeliu C., Oh Y., Lee S., Vázquez S., Pallàs M. CNS Neurosci. Ther. 2024, 30, e14511. doi: 10.1111/cns.14511
  11. Codony S., Calvó-Tusell C., Valverde E., Osuna S., Morisseau C., Loza M.I., Brea J., Pérez C., Rodríguez-Franco M.I., Pizarro-Delgado J., Corpas R., Griñán-Ferré C., Pallàs M., Sanfeliu C., Vázquez-Carrera M., Hammock B.D., Feixas F., Vázquez S. J. Med. Chem. 2021, 64, 5429–5446. doi: 10.1021/acs.jmedchem.0c01601
  12. Stoikov I.I., Antipin I.S., Burilov V.A., Kurbangalieva A.R., Rostovskii N.V., Pankova A.S., Balova I.A., Remizov Yu.O., Pevzner L.M., Petrov M.L., Vasilyev A.V., Ave-rin A.D., Beletskaya I.P., Nenajdenko V.G., Beloglazkina E.K., Gromov S.P., Karlov S.S., Magdesieva T.V., Prishchenko A.A., Popkov S.V., Terent’ev A.O., Tsap-lin G.V., Kustova T.P., Kochetova L.B., Magdalinova N.A., Krasnokutskaya E.A., Nyuchev A.V., Kuznetsova Yu.L., Fedorov A.Yu., Egorova A.Yu., Grinevk V.S., Sorokin V.V., Ovchinnikov K.L., Kofanov E.R., Kolobov A.V., Rusinov V.L., Zyryanov G.V., Nosov E.V., Bakulev V.A., Belskaya N.P., Berezkina T.V., Obydennov D.L., Sosnovskikh V.Ya., Bakhtin S.G., Baranova O.V., Doroshkevich V.S., Raskildina G.Z., Sultanova R.M., Zlotskii S.S., Dyachenko V.D., Dyachenko I.V., Fisyuk A.S., Konshin V.V., Dotsenko V.V., Ivleva E.A., Reznikov A.N., Klimochkin Yu.N., Aksenov D.A., Aksenov N.A., Aksenov A.V., Burmistrov V.V., Butov G.M., Novakov I.A., Shikhaliev Kh.S., Stolpovskaya N.V., Medvedev S.M., Kandalintseva N.V., Prosenko O.I., Menshchikova E.B., Golovanov A.A., Khashirova S.Yu. Russ. J. Org. Chem. 2024, 60, 1361–1584. doi: 10.31857/S0514749224020058
  13. Kuznetsov Ya.P., Burmistrov V.V., Butov G.M. Russ. J. Org. Chem. 2022, 58, 1429–1433. doi: 10.1134/S1070428022100074
  14. Кузнецов Д.В., Бурмистров В.В., Бутов Г.М. Известия ВолгГТУ, 2018, 222, 7–13.
  15. Новаков И.А., Орлинсон Б.С., Савельев Е.Н., Потаенкова Е.А., Махаева Т.А. Пат. 2454401 (2012) РФ. Опубликовано: 27.06.2012, бюл. № 18.

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