Abstract
Synthesis of new polycyclic thieno[2,3-b]pyridine derivatives from ethyl 3-amino-5-(2-furyl)-7,7-dimethyl-7,8-dihydro-5H-pyrano[4,3-b]thieno[3,2-e]pyridine-2-carboxylate is described.
References
Yu. A. Kvashnin, E. V. Verbitskiy, G. L. Rusinov, V. N. Charushin, Russ. Chem. Bull., 2022, 71, 1242; DOI: https://doi.org/10.1007/s11172-022-3540-0.
A. E. Fedorov, L. A. Rodinovskaya, A. M. Shestopalov, A. S. Sigeev, Russ. Chem. Bull, 2021, 70, 394; DOI: https://doi.org/10.1007/s11172-021-3099-1.
E. G. Paronikyan, Sh. Sh. Dashyan, A. S. Harutyunyan, S. S. Mamyan, E. S. Safaryan, Russ. Chem. Bull., 2022, 71, 1019; DOI: https://doi.org/10.1007/s11172-022-3503-5.
A. V. Komkov, S. V. Baranin, A. S. Dmitrenok, I. V. Zavarzin, Russ. Chem. Bull., 2022, 71, 1720; DOI: https://doi.org/10.1007/s11172-022-3582-3.
R. L. Nakamura, M. A. Burlingame, S. Yang, D. C. Crosby, D. J. Talbot, K. Chui, A. D. Frankel, A. R. Renslo, Antimicrob. Agents Chemother., 2017, 61, e02366–16; DOI: https://doi.org/10.1128/AAC.02366-16.
A. K. Mugengana, N. A. Vita, A. B. Gandt, K. Moran, G. Agyapong, L. K. Sharma, E. C. Griffith, J. Liu, L. Yang, E. Gavrish, K. E. Hevener, M. D. LaFleur, R. E. Lee, ACS Infect. Dis., 2021, 7, 1044; DOI: https://doi.org/10.1021/acsinfecdis.0c00300.
P. Lagardère, C. Fersing, N. Masurier, V. Lisowski, Pharmaceuticals, 2021, 15, 35; DOI: https://doi.org/10.3390/ph15010035.
M. D. Mashkovsky, Lekarstvenny esredstva [Medicines], Novaya Volna, Moscow, 2021, p. 1216 (in Russian).
S. Ayvaz, M. Çankaya, A. Atasever, A. Altuntas, J. Enzyme Inhib. Med. Chem., 2013, 28, 305; DOI: https://doi.org/10.3109/14756366.2011.639016.
S. T. Nquyan, S. M. Kwasny, X. Ding, S. C. Cardinale, C. T. Mccarthy, H. S. Kim, H. Nikaido, N. P. Peet, J. D. Williams, T. L. Bowlen, T. L. Opperman, Bioorg. Med. Chem., 2015, 23, 2024; DOI: https://doi.org/10.1016/j.bmc.2015.03.016.
Z. Aron, T. J. Opperman, Curr. Opin. Microbiol., 2016, 33, 1; DOI: https://doi.org/10.1016/j.mib.2016.05.007.
T. J. Opperman, S. M. Kwasny, H.-S. Kim, S. T. Nguyen, Ch. Houseweart, S. D’Souza, G. C. Walker, N. P. Peet, H. Nikaido, T. L. Bowlina, Antimicrob. Agents Chemother., 2014, 58, 722; DOI: https://doi.org/10.1128/aac.01866-13.
E. V. Babaev, Ya. I. Koval, V. B. Rybakov, E. G. Paronikyan, G. M. Stepanyan, R. G. Paronikyan, Sh. Sh. Dashyan, S. A. Rzhevsky, N. A. Shadrin, Russ. Chem. Bull., 2018, 67, 313; DOI: https://doi.org/10.1007/s11172-018-2076-9.
A. Wójcicka, Curr. Org. Chem., 2021, 25, 2740; DOI: https://doi.org/10.2174/1385272825666210812102815.
N. Kandepedu, D. G. Cabrera, S. Eudubilli, D. Taylor, Ch. Brunchwig, L. Gibhard, M. Njoroge, N. Lawrence, T. Paquet, Ch. J. Eyermann, T. Spangenberg, G. S. Basarab, L. J. Street, K. Chibale, J. Med. Chem., 2018, 61, 5692; DOI: https://doi.org/10.1021/acs.jmedchem.8b00648.
N. A. Haverkate, E. Leung, L. I. Pilkington, D. Barker, Pharmaceutics, 2021, 13, 2020; DOI: https://doi.org/10.3390/pharmaceutics13122020.
H. J. Arabshahi, M. van Rensburg, L. I. Pilkington, Ch. Y. Jeon, M. Song, L.-M. Gridel, E. Leung, D. Barker, M. V. Ross, K. P. Volcho, A. L. Zakharenko, O. I. Lavrik, J. Reynisson, Med. Chem. Comm., 2015, 6, 1987; DOI: https://doi.org/10.1039/C5MD00245A.
M. A. Elsherif, J. Appl. Pharm. Sci., 2021, 11, 118; DOI: https://doi.org/10.7324/JAPS.2021.110614.
R. M. Zaki, A. M. K. El-Dean, Sh. M. Radwan, A. S. Sayed, ACS Omega, 2020, 5, 252; DOI: https://doi.org/10.1021/acs.omega9b02604.
N. Bhardwaj, A. Pathania, P. Kumar, Curr. Tradit. Med., 2021, 7, 5; DOI: https://doi.org/10.2174/2215083805666190613125700.
V. V. Dabaeva, M. R. Bagdasaryan, A. S. Noravyan, Zh. V. Kazaryan, I. A. Dzhagatspanyan, I. M. Nazaryan, A. G. Akopyan, Pharm. Chem. J., 2016, 49, 830; DOI: https://doi.org/10.1007/s11094-016-1381-6.
V. V. Dabaeva, M. R. Bagdasaryan, A. S. Noravyan, I. A. Dzhagatspanyan, I. N. Nazaryan, A. G. Akopyan, Pharm. Chem. J., 2012, 46, 271; DOI: https://doi.org/10.1007/s11094-012-0778-0.
V. V. Dabaeva, M. R. Bagdasaryan, A. S. Noravyan, I. M. Nazaryan, A. G. Akopyan, A. A. Tadevosyan, Pharm. Chem. J., 2013, 47, 135; DOI: https://doi.org/10.1007/s11094-013-0911-8.
V. V. Dabaeva, M. R. Baghdasaryan, R. G. Paronikyan, I. M. Nazaryan, H. G. Hakobyan, L. S. Hunanyan, E. G. Paronikyan, Sh. Sh. Dashyan, Russ. J. Bioorg. Chem., 2022, 48, 125; DOI: https://doi.org/10.1134/S1068162022010034.
V. V. Dabaeva, M. R. Baghdasaryan, E. G. Paronikyan, R. A. Tamazyan, A. G. Ayvazyan, Sh. Sh. Dashyan, Russ. J. Gen. Chem., 2019, 89, 2364; DOI: https://doi.org/10.1134/S1070363219120065.
V. V. Dabaeva, M. R. Baghdasaryan, E. G. Paronikyan, Sh. Sh. Dashyan, Russ. J. Gen. Chem., 2019, 89, 847; DOI: https://doi.org/10.1134/S1070363219040340.
V. V. Dabaeva, M. R. Bagdasaryan, Sh. Sh. Dashyan, I. M. Nazaryan, A. G. Akopyan, R. G. Paronikyan, Pharm. Chem. J., 2018, 52, 844; DOI: https://doi.org/10.1007/s11094-019-1912-z.
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
The authors declare no competing interests.
Additional information
No human or animal subjects were used in this research.
Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, Vol. 72, No. 8, pp. 1802–1808, August, 2023.
Rights and permissions
About this article
Cite this article
Dabaeva, V.V., Bagdasaryan, M.R., Barkhudaryants, I.M. et al. New polyheterocycles derived from pyrano[4,3-b]thieno[3,2-e]pyridine. Russ Chem Bull 72, 1802–1808 (2023). https://doi.org/10.1007/s11172-023-3962-3
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11172-023-3962-3