RAS Chemistry & Material ScienceЖурнал органической химии Russian Journal of Organic Chemistry

  • ISSN (Print) 0514-7492
  • ISSN (Online) 3034-6304

Synthesis of New 2-Carboxamide-Substituted 5-Oxo-5,6-dihydro-4-1,3,4-thiadiazines

PII
S3034630425070024-1
DOI
10.7868/S3034630425070024
Publication type
Article
Status
Published
Authors
Volume/ Edition
Volume 61 / Issue number 7
Pages
816-820
Abstract
Based on the reaction of benzylmaleimide and -substituted 2-hydroxy-2-thioxoacetamide, a series of new 2-carboxamide-substituted 5-oxo-5,6-dihydro-4-1,3,4-thiadiazines, compounds with potential biological activity, were synthesized and characterized.
Keywords
5-оксо-5,6-дигидро-4-1,3,4-тиадиазин 2-гидразинил-2-тиоксоацетамид бензилмалеимид внутримолекулярная циклизация
Date of publication
01.07.2025
Year of publication
2025
Number of purchasers
0
Views
22

References

  1. 1. Ananikov V.P., Khokhlova E.A., Egorov M.P., Sakharov A.M., Zlotin S.G., Kucherov A.V., Kustov L.M., Gening M.L., Nifantiev N.E. Mendeleev Commun. 2015, 25, 75–82. https://doi.org/10.1016/j.mencom.2015.03.001
  2. 2. Pfeiffer W.-D., Junghans D., Saghyan A.S., Langer P. J. Heterocycl. Chem. 2014, 51, 1063. https://doi.org/10.1002/jhet.2007
  3. 3. Емельянов В.В., Иванов А.В., Саватеева Е.А., Сидорова Л.П., Цейтлер Т.А., Гетте И.Ф., Булавинцева Т.С., Данилова И.Г., Максимова Н.Е., Мочульская Н.Н., Чупахин О.Н., Черешнев В.А. Изв. АН. Сер. Хим. 2017, 66, 1873. @@Emelianov V.V., Ivanov A.V., Savateeva E.A., Sidorova L.P., Tseitler T.A., Gette I.F., Bulavintseva T.S., Danilova I.G., Maksimova N.E., Mochul'skaya N.N., Chupakhin O. N., Chereshnev V.A. Russ. Chem. Bull., Int. Ed. 2017, 66, 1873. https://doi.org/10.1007/s11172-017-1960-z
  4. 4. Сидорова Л.П., Цейтлер Т.А., Перова Н.М., Емельянов В.В., Саватеева Е.А., Максимова Н.Е., Мочульская Н.Н., Черешнев В.А., Чупахин О.Н. Хим.-фармац. ж. 2015, 49, 8–12. @@Sidorova L.P., Tseitler T.A., Perova N.M., Emel'yanov V.V., Savateeva E.A., Maksimova N.E., Mochul'skaya N.N., Chereshnev V.A., Chupakhin O.N. Pharm. Chem. J. 2015, 49, 501–505. https://doi.org/10.1007/s11094-015-1314-9
  5. 5. Shevelev O.B., Illarionova N.B., Petrovski D.V., Sarapultsev A.P., Chupakhin O.N., Moshkin M.P. PLoS One. 2017, 12, e0180739. https://doi.org/10.1371/journal.pone.0180739
  6. 6. Abdel-Aziem A.J. Heterocycl. Chem. 2015, 52, 251. https://doi.org/10.1002/jhet.2390
  7. 7. Prakash O., Aneja D.K., Hussain K., Lohan P., Ranjan P., Arora S., Sharma C., Aneja K.R. Eur. J. Med. Chem. 2011, 46, 5065–5073. https://doi.org/10.1016/j.ejmech.2011.08.019
  8. 8. Hussein M.A., Shaker R.M., Ameen M.A., Mohammed M.F. Arch. Pharm. Res. 2011, 34, 1239–1250. https://doi.org/10.1007/s12272-011-0802-z
  9. 9. Sarıgüney A.B., Kocabaş E., Erci F., Torlak E., Coşkun, A.J. Heterocycl. Chem. 2018, 55, 2107. https://doi.org/10.1002/jhet.3254
  10. 10. Radini I.A.M. Molecules. 2018, 23, 2092. https://doi.org/10.3390/molecules23092092
  11. 11. Sibley G.E.M., Malström L.J., Larsson J.M. WO Patent 2017009651.
  12. 12. Sagar S.R., Singh D.P., Panchal N.B., Das R.D., Pandya D.H., Sudarsanam V., Nivsarkar M., Vasu K.K. ACS Chem. Neurosci. 2018, 9, 1663–1679. https://doi.org/10.1021/acschemneuro.8b00063
  13. 13. Fahmy A.F.M., Rizk S.A., Hemdan M.M., El-Sayed A.A., Hassaballah A.I. J. Heterocycl. Chem. 2018, 55, 2545. https://doi.org/10.1002/jhet.3308
  14. 14. Čačić M., Pavić V., Molnar M., Šarkanj B., Has-Schön E. Molecules. 2014, 19, 1163–1177. https://doi.org/10.3390/molecules19011163
  15. 15. Yang Y., Feng Z., Jiang J., Yang Y., Pan X., Zhang P. Chem. Pharm. Bull. 2011, 59, 1016–1019. https://doi.org/10.1248/cpb.59.1016
  16. 16. Ørstavik Ø., Ata S., Riise J., Dahl C., Andersen G. Ø., Levy F., Skomedal T., Osnes J. B., Qvigstad E. Br. J. Pharmacol. 2014, 171, 5169–5181. https://doi.org/10.1111/bph.12647
  17. 17. Патент РФ, RU 2 822 231 С1, Бюлл. изобрет., 2024, 20.
  18. 18. Komendantova A.S., Ivanova K.A., Lyssenko K.V., Volkova Yu.A., Zavarzin I.V., Chem. Heterocycl. Compds. 2019, 55, 665. https://doi.org/10.1007/s10593-019-02514-5
  19. 19. Яровенко В.Н., Широков А.В., Крупинова О.Н., Заварзин И.В., Краюшкин М.М. ЖОрХ. 2003, 39, 1204. @@Yarovenko V.N., Shirokov A.V., Krupinova O.N., Zavarzin I.V., Krayushkin M.M. Russ. J. Org. Chem. 2003, 39, 1133. https://doi.org/10.1023/B:RUJO.0000010181.01921.77
QR
Translate

Indexing

Scopus

Scopus

Scopus

Crossref

Scopus

Higher Attestation Commission

At the Ministry of Education and Science of the Russian Federation

Scopus

Scientific Electronic Library