Synthesis of 2-alkyl-1,2,4-triazolo[3,4-a]isoquinolin-2-ium bromides and hexafluorophosphates
- Autores: Ermakova L.S.1, Leont’ev N.O.2, Denisov M.S.1, Borisova I.А.2, Dmitriev М.V.2, Glushkov V.A.1,2
-
Afiliações:
- Institute of Technical Chemistry, Perm Federal Research Center, Ural Branch of the Russian Academy of Sciences
- Perm State National Research University
- Edição: Volume 94, Nº 10 (2024)
- Páginas: 1021-1031
- Seção: Articles
- URL: https://journals.rcsi.science/0044-460X/article/view/281023
- DOI: https://doi.org/10.31857/S0044460X24100023
- EDN: https://elibrary.ru/RFQPWH
- ID: 281023
Citar
Resumo
Alkylation of 1,2,4-triazolo[3,4-a]isoquinolines with 1-bromoalkanes was carried out under microwave synthesis conditions; the resulting 2-alkyl-1,2,4-triazolo[3,4-a]isoquinolin-2-ium bromides were converted into hexafluorophosphates and characterized by high-resolution mass spectrometry, 1H, 13C NMR spectroscopy and X-ray diffraction analysis.
Palavras-chave
Texto integral

Sobre autores
L. Ermakova
Institute of Technical Chemistry, Perm Federal Research Center, Ural Branch of the Russian Academy of Sciences
Email: glusha55@gmail.com
ORCID ID: 0009-0008-1397-6631
Rússia, 614068, Perm
N. Leont’ev
Perm State National Research University
Email: glusha55@gmail.com
ORCID ID: 0009-0000-9777-0658
Rússia, 614099, Perm
M. Denisov
Institute of Technical Chemistry, Perm Federal Research Center, Ural Branch of the Russian Academy of Sciences
Email: glusha55@gmail.com
ORCID ID: 0000-0002-8817-0543
Rússia, 614068, Perm
I. Borisova
Perm State National Research University
Email: glusha55@gmail.com
ORCID ID: 0000-0002-2261-8122
Rússia, 614099, Perm
М. Dmitriev
Perm State National Research University
Email: glusha55@gmail.com
ORCID ID: 0000-0002-0731-3400
Rússia, 614099, Perm
V. Glushkov
Institute of Technical Chemistry, Perm Federal Research Center, Ural Branch of the Russian Academy of Sciences; Perm State National Research University
Autor responsável pela correspondência
Email: glusha55@gmail.com
ORCID ID: 0000-0001-6493-7351
Rússia, 614068, Perm; 614099, Perm
Bibliografia
- Pan Y., Tian R., Chen Y., Wang L., Qin H., Wang J. // Tetrahedron. 2023. Vol. 148. P. 133688. doi 10.1016/ j.tet.2023.133688
- Zhang W., Jiang R., Mu Y., Hong Y., Man Y., Yang Z., Tang D. // Tetrahedron Lett. 2023. Vol. 114. P. 154256. doi: 10.1016/j.tetlet.2022.154256
- Глушков В.А., Шкляев Ю.В., Майорова О.А., Постаногова Г.А., Фешина Е.В. // ХГС. 2000. Т. 36. С. 380; Glushkov V.A., Shklyaev Yu.V., Maiorova O.A., Postanogova G.A., Feshina E.V. // Chem. Heterocycl. Compd. 2000. Vol. 36. P. 319. doi: 10.1007/BF02256870
- Deady L.W., Devine S.M. // J. Heterocycl. Chem. 2004. Vol. 41. P. 549. doi: 10.1002/jhet.5570410411
- Chen Z., Chen S., Qui Z., Lin B., Yao Y., Weng Z. // J. Org. Chem. 2024. Vol. 89. P. 7163. doi 10/1021/acs.joc.4c00557
- Yount J., Morris M., Henson N., Zeller M., Byrd E.F.C., Piercey D.G. // Chem. Eur. J. 2024. Vol. 30. P. e202400661. doi: 10.1002/chem.202400661
- Badr S.M.I., Barwa R.M. // Bioorg. Med. Chem. 2011. Vol. 19. P. 4506. doi: 10.1016/j.bmc.2011.06.024
- Zhao P.-L., Duan A.-N., Zou M., Yang H.-K., You W.-W., Wu S.-G. // Bioorg. Med. Chem. Lett. 2012. Vol. 22. P. 4471. doi: 10.1016/j.bmcl.2012.03.023
- Yan X., Zhang C., Gao L.-X., Liu M.-M., Yang Y.-T., Yu L.-J., Zhou Y.-B., Milaneh S., Zhu Y.-L., Li J., Wang W.-L. // Eur. J. Med. Chem. 2024. Vol. 265. P. 116027. doi: 10.1016/j.ejmech.2023.116027
- Feitosa L.M., Franca R.R.F., Ferreira M. de L.G., Aguiar A.C.C., de Souza G.E., Maluf S.E.C., de Souza J.O., Zapata L., Duarte D., Morais I., Nogueira F., Nonato M.C., Pinheiro L.C.S., Guido R.V.C., Boechat N. // Eur. J. Med. Chem. 2024. Vol. 267. P. 116163. doi 10.1016/ j.ejmech.2024.116163; Ali I., Cha H.J., Lim B., Chae C.H., Youm J., Park W.J., Lee S.H., Kim J.H., Jeong D., Lim J.K., Hwang Y.-H., Roe J.-S., Woo J.-S., Lee K., Choi G. // Eur. J. Med. Chem. 2024. Vol. 265. 116052. doi 10.1016/ j.ejmech.2023.116052
- Ali I., Cha H.J., Lim B., Chae C.H., Youm J., Park W.J., Lee S.H., Kim J.H., Jeong D., Lim J.K., Hwang Y.-H., Roe J.-S., Woo J.-S., Lee K., Choi G. // Eur. J. Med. Chem. 2024. Vol. 265. 116052. doi 10.1016/ j.ejmech.2023.116052
- Носова Э.В., Копотилова А.Е., Иванькина М.А., Мошкина Т.Н., Копчук Д.С. // Изв. АН. Сер. хим. 2022. Т. 71. № 7. С. 1483; Nosova E.V., Kopotilova A.E., Ivan’kina M.A., Moshkina T.N., Kopchuk D.S. // Russ. Chem. Bull. 2022. Vol. 71. N 7. P. 1483. doi: 10.1007/s11172-022-3554-7
- Shtaitz Ya.K., Ladin E.D., Kopchuk D.S., Khalymbadzha I.A., Gaviko V.S., Zyryanov G.V., Antonenko D.V., Ostrovskii V.A., Rusinov V.L. // Russ. J. Gen. Chem. 2024. Vol. 94. P. 749. doi: 10.1134/S1070363224040029
- Русинов В.Л., Чарушин В.Н., Чупахин О.Н. // Изв. АН. Сер. хим. 2018. № 4. С. 573; Rusinov V.L., Charushin V.N., Chupakhin O.N. // Russ. Chem. Bull. 2018. Vol. 67. N 4. P. 573. doi: 10.1007/s11172-018-2113-8
- Машковский М.Д. Лекарственные средства. М.: Новая волна, 2019. С. 30, 83, 84.
- Ермакова Л.С., Грачева В.С., Майорова О.А., Дмитриев М.В., Белоглазова Ю.А., Глушков В.А. // Изв. АН. Сер. хим. 2024. Т. 73. С. 1072; Ermakova L.S., Gracheva V.S., Maiorova O.A., Dmitriev M.V., Beloglazova Yu.A., Glushkov V.A. // Russ. Chem. Bull. 2024. Vol. 73. P. 1072. doi: 10.1007/s11172-024-4222-x
- CrysAlisPro, Rigaku Oxford Diffraction, 2022. Version 1.171.42.74a.
- Sheldrick G.M. // Acta Crystallogr. (A). 2015. Vol. 71. P. 3. doi: 10.1107/S2053273314026370
- Sheldrick G.M. // Acta Crystallogr. (C). 2015. Vol 71. P. 3. doi: 10.1107/S2053229614024218
- Dolomanov O.V., Bourhis L.J., Gildea R.J., Howard J.A.K., Puschmann H.J. // Appl. Cryst. 2009. Vol 42. P. 339. doi: 10.1107/S0021889808042726
Arquivos suplementares
