Synthesis of New Condensed Derivatives of Thieno[3,2-d]-pyrimidines Based on 7,7-Dimethyl-2-mercapto-4-(2-furyl)-3-cyano-7,8-dihydro-5H-pyrano[4,3-b]pyridine
- Авторлар: Dabaeva V.V.1, Barkhudaryants I.M.1, Paronikyan E.G.1, Dashyan S.S.1, Baghdasaryan M.R.1
-
Мекемелер:
- Scientific and Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia
- Шығарылым: Том 61, № 1 (2025)
- Беттер: 102-108
- Бөлім: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://journal-vniispk.ru/0514-7492/article/view/291951
- DOI: https://doi.org/10.31857/S0514749225010086
- EDN: https://elibrary.ru/AFKMTG
- ID: 291951
Дәйексөз келтіру
Аннотация
Methods for the synthesis of new condensed thieno[3,2-e]pyridines and thieno[3,2-d]pyrimidines have been developed. The reaction of 7,7-dimethyl-2-mercapto-4-(2-furyl)-3-cyano-7,8-dihydro-5H-pyrano[4,3-b]pyridine with chloroacetic acid amides has been established depending on temperature. It has been shown that at high temperatures alkylation and intramolecular cyclization (one pot reaction) occur with the formation of pyrano[4,3-b]thieno[3,2-e]pyridines. New derivatives of condensed tetracyclic thieno[3,2-d]pyrimidines were synthesized by condensation of pyrano[4,3-b]thieno[3,2-e]pyridine carboxamides with orthoformic acid triethyl ester.
Негізгі сөздер
Толық мәтін

Авторлар туралы
V. Dabaeva
Scientific and Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia
Хат алмасуға жауапты Автор.
Email: valya.dabayeva@mail.ru
ORCID iD: 0000-0003-2980-2552
Армения, 26, Azatutyan Ave., Yerevan, 0014
I. Barkhudaryants
Scientific and Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia
Email: valya.dabayeva@mail.ru
ORCID iD: 0000-0002-4620-6034
Армения, 26, Azatutyan Ave., Yerevan, 0014
E. Paronikyan
Scientific and Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia
Email: valya.dabayeva@mail.ru
ORCID iD: 0000-0002-6048-3599
Армения, 26, Azatutyan Ave., Yerevan, 0014
Sh. Dashyan
Scientific and Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia
Email: valya.dabayeva@mail.ru
ORCID iD: 0000-0002-6365-3725
Армения, 26, Azatutyan Ave., Yerevan, 0014
M. Baghdasaryan
Scientific and Technological Center of Organic and Pharmaceutical Chemistry of the National Academy of Sciences of the Republic of Armenia
Email: valya.dabayeva@mail.ru
ORCID iD: 0000-0001-7092-0556
Армения, 26, Azatutyan Ave., Yerevan, 0014
Әдебиет тізімі
- Chiacchio M. A., Iannazzo D., Romeo R., Giofrè S. V., Legnani, L. Curr. Med. Chem., 2019, 26 (40), 7166–7195. doi: 10.2174/0929867325666180904125400
- El‐Mekabaty A., Fouda A.E.A.S., Shaaban I.E. J. Heterocycl. Chem., 2020, 57 (7), 2928–2935. doi: 10.1002/jhet.4002
- Zaki R.M., Kamal El-Dean A.M., Radwan S.M., Ammar M.A. Russ. J. Bioorg. Chem., 2022, 48 (Suppl 1), S121–S135. doi: 10.1134/S1068162023010314
- Alenazi N.A., Alharbi H., Qarah A.F., Alsoliemy A., Abualnaja M.M., Karkashan A., Abbas B., El-Metwaly N.M. Arab. J. Chem., 2023, 16 (11), 105226. doi: 10.1016/j.arabjc.2023.105226
- Mohi El-Deen E.M., El-Gwaad A., Amina A., Anwar M.M. Egypt. J. Chem., 2023, 66 (2), 231–242. doi: 10.21608/EJCHEM.2022.136967.6042
- Saber A.F., Kamal El‐Dean A.M., Redwan S.M., Zaki R.M. J. Chinese Chem. Soc., 2020, 67 (7), 1239–1246. doi: 10.1002/jccs.201900374
- Binsaleh N.K., Wigley C.A., Whitehead K.A., van Rensburg M., Reynisson J., Pilkington L.I., Barker D., Jones S., Dempsey-Hibbert N.C. Eur. J. Med. Chem., 2018, 143, 1997–2004. doi: 10.1016/j.ejmech.2017.11.014
- Liu Y.F., Fu S.Q., Yan Y.C., Gong B.B., Xie W.J., Yang X.R., Sun T., Ma M. Drug Des. Devel. Ther. 2021, 15, 639–649. doi: 10.2147/DDDT.S291369
- Sarker D., Ang J.E., Baird R., Kristeleit R., Shah K., Moreno V., Clarke P.A., Raynaud F.I., Levy G., Ware J.A., Mazina K., Lin R., Wu J., Fredrickson J., Spoerke J.M., Lackner M.R., Yan Y., Friedman L.S., Kaye S.B., Derynck M.K., Workman P., de Bonoet J.S. Clin. Cancer Res. 2015, 21, 77–86. doi: 10.1158/1078-0432.CCR-14-0947
- Kim D.W., Lee D.H., Han J.Y., Lee J., Cho B.C., Kang J.H., Lee K. H., Cho E. K., Kim J.-S., Min Y. J., Cho J.Y., An H.J., Kim H.-G., Lee K.H., Kim B.-S., Jang I.-J., Yoon S., Han O.P., Noh Y.S., Hong K.Y., Park K. Lung Cancer. 2019, 135, 66–72. doi: 10.1016/j.lungcan.2019.07.007
- Дабаева В.В., Багдасарян М.Р., Бархударянц И.М., Пароникян Е.Г., Паносян Г.А., Дашян Ш.Ш. ЖОХ, 2022, 92 (9), 1442–1448. [Dabaeva V.V., Bagdasaryan M.R., Barkhudaryants I.M., Paronikyan E.G., Panosyan G.A., Dashyan Sh.Sh. Russ. J. Gen. Chem., 2022, 92, 1686–1691. doi: 10.1134/S1070363222090109]
