Synthesis and optical properties of 6-alkylamino-2-amino-4-(4-(dimethylamino)phenyl)-pyridine-3,5-dicarbonitriles

Мұқаба

Дәйексөз келтіру

Толық мәтін

Ашық рұқсат Ашық рұқсат
Рұқсат жабық Рұқсат берілді
Рұқсат жабық Рұқсат ақылы немесе тек жазылушылар үшін

Аннотация

6-Alkylamino-2-amino-4-(4-(dimethylamino)phenyl)pyridine-3,5-dicarbonitriles were obtained by the reaction of primary and secondary amines with 2-amino-6-chloro-4-(4-(dimethylamino)phenyl)pyridine-3,5-dicarbonitrile synthesized by three stages from dimethylaniline. The study of the spectral-luminescent properties showed the presence of fluorescence in solutions with a maximum in the region of 432–473 nm and a quantum yield of up to 29.5%, and in the solid state with a maximum in the region of 446–472 nm.

Авторлар туралы

E. Ramskaya

Ulyanov Chuvash State University

Moskovskii prosp., 15, Cheboksary, 428015 Russia

A. Alekseeva

Ulyanov Chuvash State University

Moskovskii prosp., 15, Cheboksary, 428015 Russia

S. Zhitar

Ulyanov Chuvash State University

Moskovskii prosp., 15, Cheboksary, 428015 Russia

N. Yaschenko

Ulyanov Chuvash State University

Moskovskii prosp., 15, Cheboksary, 428015 Russia

E. Zinovieva

Ulyanov Chuvash State University

Moskovskii prosp., 15, Cheboksary, 428015 Russia

I. Bardasov

Ulyanov Chuvash State University

Email: bardasov.chem@mail.ru
Moskovskii prosp., 15, Cheboksary, 428015 Russia

Әдебиет тізімі

  1. Alshammari O.A.O., Azzam E.M.S., Alhar M.S., Alanazi K.D., Aljuhani S.A.A., Elsofany W.I. Mol. 2024, 29 (5), 1139. doi: 10.3390/MOLECULES29051139
  2. Lavanya M., Asharani I.V., Thirumalai D. Chem. Biol. Drug Des. 2019, 93 (4), 464–472. doi: 10.1111/cbdd.13434
  3. Samadi A., Marco-Contelles J., Soriano E., Álvarez-Pérez M., Chioua M., Romero A., González-Lafuente L., Gandía L., Roda J.M., López M.G., Villar- roya M., García A.G., Ríos C.D.L. Bioorg. Med. Chem. 2010, 18 (16), 5861–5872. doi: 10.1016/J.BMC.2010.06.095
  4. Cocco M.T., Congiu C., Lilliu V., Onnis V. Bioorg. Med. Chem. 2007, 15 (4), 1859–1867. doi: 10.1016/J.BMC.2006.11.031
  5. Leitonas K., Vigante B., Volyniuk D., Bucinskas A., Dimitrijevs P., Lapcinska S., Arsenyan P., Grazulevi- cius J.V. Beilstein J. Org. Chem. 2023, 19 (1), 1867–1880. doi: 10.3762/BJOC.19.139
  6. Arsenyan P., Vigante B., Leitonas K., Volyniuk D., Andruleviciene V., Skhirtladze L., Belyakov S., Grazulevicius J.V. J. Mater. Chem. C 2021, 9 (11), 3928–3938. doi: 10.1039/D0TC05745B
  7. Vigante B., Leitonas K., Volyniuk D., Andruleviciene V., Simokaitiene J., Ivanova A., Bucinskas A., Grazulevi- cius J.V., Arsenyan P. Chem. – A Eur. J. 2019, 25 (13), 3325–3336. doi: 10.1002/chem.201805323
  8. Bardasov I.N., Alekseeva A.Yu. Russ. J. Org. Chem. 2023, 59 (9), 1502–1510. doi: 10.1134/S1070428023090075
  9. Ramskaya E.N., Kayukov Y.S., Kayukova O.V, Lyshchikov A.N., Alekseeva A.U., Bardasov I.N. Russ. J. Gen. Chem. 2024, 94 (7), 1666–1671. doi: 10.1134/S1070363224070089
  10. Alekseeva A.Yu., Kayukov Ya.S., Ramskaya E.N., Bardasov I.N. Russ. J. Gen. Chem. 2024, 94 (1), 73–80. doi: 10.1134/S1070363224010079
  11. Koner R.R., Sinha S., Kumar S., Nandi C.K., Ghosh S. Tetrahedron Lett. 2012, 53 (18), 2302–2307. doi: 10.1016/j.tetlet.2012.02.094
  12. Shylaja A., Roja S.S., Priya R.V., Kumar R.R. J. Org. Chem. 2018, 83 (22), 14084–14090. doi: 10.1021/acs.joc.8b01991
  13. Santharam Roja S., Shylaja A., Kumar R.R. ChemistrySelect 2020, 5 (7), 2279–2283. doi: 10.1002/slct.201904425
  14. Shylaja A., Rubina S.R., Roja S.S., Kumar R.R. Dye. Pigment. 2020, 174 (November 2019), 108062. doi: 10.1016/j.dyepig.2019.108062
  15. Sarkar S., Das D.K., Khan A.T. RSC Adv. 2014, 4 (96), 53752–53760. doi: 10.1039/C4RA08237K
  16. Raghukumar V., Thirumalai D., Ramakrishnan V.T., Karunakara V., Ramamurthy P. Tetrahedron 2003, 59 (21), 3761–3768. doi: 10.1016/S0040-4020(03)00507-6
  17. Boruah A., Deb M.L., Thakuria R., Baruah P.K. Org. Biomol. Chem. 2024, 22 (43), 8608–8616. doi: 10.1039/D4OB01343C
  18. Ryzhkova Y.E., Elinson M.N. Arkivoc 2022, 2022 (5), 126–134. doi: 10.24820/ARK.5550190.P011.703
  19. Samadi A., Chioua M., Bolea I., De Los Ríos C., Iriepa I., Moraleda I., Bastida A., Esteban G., Unzeta M., Gálvez E., Marco-Contelles J. Eur. J. Med. Chem. 2011, 46 (9), 4665–4668. doi: 10.1016/J.EJMECH.2011.05.048
  20. Leitonas K., Vigante B., Volyniuk D., Bucinskas A., Dimitrijevs P., Lapcinska S., Arsenyan P., Grazulevicius J. V. Beilstein J. Org. Chem. 19139 2023, 19 (1), 1867–1880. doi: 10.3762/BJOC.19.139
  21. Catarzi D., Varano F., Varani K., Vincenzi F., Pasquini S., Dal Ben D., Volpini R., Colotta V. Pharmaceuticals. 2019, 12 (4), 159. doi: 10.3390/PH12040159
  22. Shigemitsu Y., Wang B.C., Nishimura Y., Tominaga Y. Dye. Pigment. 2012, 92 (1), 580–587. doi: 10.1016/J.DYEPIG.2011.06.015
  23. Brouwer A.M. Pure Appl. Chem. 2011, 83 (12), 2213–2228. doi: 10.1351/PAC-REP-10-09-31

Қосымша файлдар

Қосымша файлдар
Әрекет
1. JATS XML

© Russian Academy of Sciences, 2025