- 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
- 26
References
- 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. Pfeiffer W.-D., Junghans D., Saghyan A.S., Langer P. J. Heterocycl. Chem. 2014, 51, 1063. https://doi.org/10.1002/jhet.2007
- 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. 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. 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. Abdel-Aziem A.J. Heterocycl. Chem. 2015, 52, 251. https://doi.org/10.1002/jhet.2390
- 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. 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. 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. Radini I.A.M. Molecules. 2018, 23, 2092. https://doi.org/10.3390/molecules23092092
- 11. Sibley G.E.M., Malström L.J., Larsson J.M. WO Patent 2017009651.
- 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. 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. Čačić M., Pavić V., Molnar M., Šarkanj B., Has-Schön E. Molecules. 2014, 19, 1163–1177. https://doi.org/10.3390/molecules19011163
- 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. 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. Патент РФ, RU 2 822 231 С1, Бюлл. изобрет., 2024, 20.
- 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. 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
