Synthesis, structure and reactions of substituted 2-aminotetrahydrochynoline-3-carbonitriles
- Авторлар: Nikulin A.V.1, Vasilkova N.O.1, Krivenko A.P.1
-
Мекемелер:
- Saratov National Research State named after N.G. Chernyshevsky (SSU)
- Шығарылым: Том 60, № 6 (2024)
- Беттер: 69-77
- Бөлім: Articles
- URL: https://clinpractice.ru/0514-7492/article/view/676675
- DOI: https://doi.org/10.31857/S0514749224060064
- EDN: https://elibrary.ru/QZTAGE
- ID: 676675
Дәйексөз келтіру
Аннотация
A series of substituted 2-aminotetrahydroquinolinecarbonitriles was obtained by three-component condensation of diaryl(hetaryl)methylidenecyclohexanones, malononitrile and ammonium acetate. Factors influencing the selectivity of reactions and the route of product formation have been identified. The interaction of aminoquinoline carbonitriles with acetic anhydride under acid catalysis conditions led to the formation of substituted hexahydropyrimido[4,5-b]quinolinones. The structure of the compounds was established using IR, 1H, 13C NMR spectra and two-dimensional correlations HSQC spectroscopy.
Негізгі сөздер
Авторлар туралы
A. Nikulin
Saratov National Research State named after N.G. Chernyshevsky (SSU)
Email: vasilkovano@mail.ru
ORCID iD: 0000-0002-2123-4960
Institute of Chemistry
Ресей, ul. Astrakhanskaya, 83/1, Saratov, 410012N. Vasilkova
Saratov National Research State named after N.G. Chernyshevsky (SSU)
Хат алмасуға жауапты Автор.
Email: vasilkovano@mail.ru
ORCID iD: 0000-0001-9437-0704
Institute of Chemistry
Ресей, ul. Astrakhanskaya, 83/1, Saratov, 410012A. Krivenko
Saratov National Research State named after N.G. Chernyshevsky (SSU)
Email: vasilkovano@mail.ru
ORCID iD: 0000-0003-3277-4556
Institute of Chemistry
Ресей, ul. Astrakhanskaya, 83/1, Saratov, 410012Әдебиет тізімі
- Hawas U.W., Al-Omar M.A., Amr A.E.-G.E., Hammam A.E.-F.G. Am. J. Appl. Sci. 2011, 8, 945–952. doi: 10.3844/AJASSP.2011.945.952
- El-Gamal К.М., El-Morsy А.М., Saad А.М., Eissa I.H., Alswah M.J. Mol. Struct. 2018, 1166, 15-33. doi: 10.1016/j.molstruc.2018.04.010
- Perin N., Nhili R., Ester K., Laine W., Karminski-Zamola G., Kralj M., David-Cordonnier M.H., Hranjec M. J. Med. Chem. 2014, 80, 218-227. doi: 10.1016/j.ejmech.2014.04.049
- Bayomi S.M., El-Kasher H.A., El-Ashmawy M.B., Nasr M.N.A., El-Sherbeny M.A. Eur. J. Med. Chem. 2015, 101, 584-594. doi: 10.1016/j.ejmech.2015.07.014
- Karad S.C., Purohit V.B., Raval D.K., Kalaria P.N., Avalani J.R., Thakor P., Thakkar V.R. RSC Advances. 2012, 5, 1-12. doi: 10.1039/C5RA00388A
- Khan S.A., J. Fluoresc. 2017, 27, 929-937. doi: 10.1007/s10895-017-2028-z
- Takla F.N., Farahat A.A., El-Sayed M.A.-A. Intern. J. Org. Chem. 2017, 7, 369-388. doi: 10.4236/ijoc.2017.74030
- Rane B.S., Kazi M.A., Bagul S.M., Shelar D.P., Toche R.B., Jachak M.N. J. Fluoresc. 2010, 20, 415-420. doi: 10.1007/s10895-009-0557-9
- Mansour A.M., El-Taweel F.M.A., Abu El-Enein R.A.N., El-Menyawy E.M. J. Electron. Mater. 2017, 46, 6957-6964. doi: 10.1007/s11664-017-5739-7
- Al-Ahmary K.M., Mekheimer R.A., Alenezi M.S., Hamada N.M.M., Habeeb M.M. J. Mol. Liq. 2018, 249, 501-510. doi: 10.1016/j.molliq.2017.11.071
- Sheikhhosseini E., Farrokhi E., Bigdeli M.A. J. Saudi Chem. Soc. 2016, 20, S227-S230. doi: 10.1016/j.jscs.2012.09.018
- Nikulin A.V., Meshcheryakova A.A., Sklyar A.E., Vasilkova N.O., Sorokin V.V., Krivenko A.P. Rus. J. Org. Chem. 2021, 57, 1650-1655. doi: 10.1134/S1070428021100134
Қосымша файлдар
