RAS Chemistry & Material ScienceЖурнал органической химии Russian Journal of Organic Chemistry

  • ISSN (Print) 0514-7492
  • ISSN (Online) 3034-6304

Method of Synthesis of Quinoline Derivatives Based on Ethyl-3-(4-Methyl-2-Oxo-1,2-Dihydroquinoline-3-yl)Propanoates

PII
S3034630425120134-1
DOI
10.7868/S3034630425120134
Publication type
Article
Status
Published
Authors
Volume/ Edition
Volume 61 / Issue number 12
Pages
1769-1774
Abstract
A convenient and accessible method was used to synthesize novel heterocyclic hybrid systems: 3-(2-(1H-benzo[d]imidazol-2-yl)ethyl)-4-methylquinolin-2(1H)-ones, 3-(2-(benzo[d]oxazol-2-yl)ethyl)-4-methylquinolin-2(1H)-ones, and 3-(2-(benzo[d]thiazol-2-yl)ethyl)-4-methylquinolin-2(1H)-ones. The synthesis was carried out by reacting ethyl 3-(4-methyl-2-oxo-1,2-dihydroquinolin-3-yl)propanoates, substituted in the benzene ring, with α-phenylenediamine, α-aminophenol, and α-aminobenzenedithiol.
Keywords
хинолин о-фенилендиамин о-аминофенол о-аминобензотиол бензимидазол бензоксазол бензоксазинон полифосфорная кислота (ПФК) гетероциклический фрагмент гетероциклические гибриды
Date of publication
01.12.2025
Year of publication
2025
Number of purchasers
0
Views
26

References

  1. 1. Khan S.J. Arch. Chem. Res. 2022, 6, 23. Available in: https://www.primescholars.com/archives-in-chemical-research.html
  2. 2. Woods E. Am. J. Physiol., Biochem. Pharmacol. 2023, 13, 1. Available in: https://www.ajpbp.com/ajpbp-articles/organic-chemistry-the-basis-for-understanding-biological-substances.pdf
  3. 3. Amin A., Qadir T., Sharma P.K., Jeelani I., Abe H. Open J. Med. Chem. 2022, 16, e187410452209010(1–27). https://doi.org/10.2174/18741045-v16-e2209010
  4. 4. Asran M., El-Helw E.A.E, Azab M.E., Ramadan S.K., Helal M.H. J. Iran. Chem. Soc. 2023, 20, 3023–3032. https://doi.org/10.1007/s13738-023-02894-8
  5. 5. Versha R., Singh L., Rana R., Bendi A. ChemistrySelect. 2022, 7, 46, e202203648. https://doi.org/10.1002/slct.202203648
  6. 6. Li M., Chen X., Deng Y., Lu J. RSC Advances. 2021, 11, 38060–38078. https://doi.org/10.1039/D1RA06155K
  7. 7. Matada В.S., Pattanashettar R., Yernale N.G. Bioorg. Med. Chem. 2021, 32, 115973–116098. https://doi.org/10.1016/j.bmc.2021.116098
  8. 8. Ajani O.O., Iyaye S.T., Ademosun O.T. (Review Article) RSC Advances. 2022, 12, 18594–18614. https://doi.org/10.1039/D2RA02896D
  9. 9. Panchal N.B., Vaghela V.M. Oriental J. Chem. 2023, 39 (3), 546–567. https://doi.org/10.13005/ojc/390303
  10. 10. Ferreira L.M., García-García P., García P.A., Castro M.A. Eur. J. Pharm. Sci. 2025, 209, 107097. https://doi.org/10.1016/j.ejps.2025.107097
  11. 11. Behera S., Mohanty P., Behura R., Nath B., Barick A.K., Jali B.R., Biointerface Res. Appl.Chem. 2022, 12 (5), 6078–6092. https://doi.org/10.33263/BRIAC125.60786092
  12. 12. Mishra P., Kumar A., Sharma U.C., Saxena A., Prabahar A.E., Gupta S., Verma A.K. Int. J. Health Sci, 2022, 6 (S3), 2016–2040. https://doi.org/10.53730/ijhs.v6nS3.5918
  13. 13. Hernández-Ayala L.F., Guzmán-López E.G., Galano A. Antioxidants. 2023, 12 (10), 1853 (1–17). https://doi.org/10.3390/antiox12101853
  14. 14. Asran M., El-Helw E.A.E., Azab M.E., Ramadan S.K., Helal M.H. J. Iran. Chem. Soc. 2023, 20, 3023–3032. https://doi.org/10.1007/s13738-023-02894-8
  15. 15. Abdanne W., Mulugeta E. RSC Advances. 2020, 10 (35), 20784–20793. https://doi.org/10.1039/D0RA03763J
  16. 16. Ravindar L., Hasbullah S.A., Rakesh K.P., Raheem S., Agustar H.K., Ismail N., Ling L.Y., Hassan N.I. Eur. J. Med. Chem. 2024, 264, 116043. https://doi.org/10.1016/j.ejmech.2023.116043
  17. 17. Saxena A., Majee S., Ray D., Saha B. Bioorg. Med. Chem. 2024, 103, 117681. https://doi.org/10.1016/j.bmc.2024.117681
  18. 18. Lilienkamp A., Mato J., Wan B., Wang Y., Franzblau S.G., Kozikowski A.P. J. Med. Chem. 2009, 52 (7), 2109–2118. https://doi.org/10.1021/jm900003c
  19. 19. Diaconu D., Antoci V., Mangalagiu V., Amariucai-Mantu D., Mangalagiu I.I. Sci. Reports. 2022, 12, 16988 (1–17). https://doi.org/10.1038/s41598-022-21435-6
  20. 20. Khalifa Z., Upadhyay R., Kumari P., Patel B.A. Intech. Open. 2023, Available in: http://dx.doi.org/10.5772/intechopen.108949
  21. 21. Khan Y., Iqbal S., Shah M., Maalik A., Hussain R., Khan S., Khan I., Pashameah R.A., Alzahrani E., Farouk A.E., Alahmdi M.I., Abd-Rabboh H.S.M. Front. Chem. 2022, 10, 995820 (1–11). https://doi.org/10.3389/fchem.2022.995820
  22. 22. Santali E.Y. Egypt. J. Chem. 2023, 66 (7), 527–551. https://doi.org/0.21608/EJCHEM.2022.167867.7074
  23. 23. Srinivasa S.B., Poojary B., Kalal B.S., Brahmavara U., Vaishali D., Das A.J., Kalenga T.M., Paidikondala M., Shankar M.K. Results in Chem. 2024, 9, 101631 (1–10). https://doi.org/10.1016/j.rechem.2024.101631
  24. 24. Insuasty D., Vidal O., Bernal A., Marquez E., Guzman J., Insuasty B., Quiroga J., Svetaz L., Zacchino S., Puerto G., Abonia R. Antibiotics. 2019, 8 (4), 239 (1–11). https://doi.org/10.3390/antibiotics8040239
  25. 25. Chau N.B., Vu T.K., Lett. Drug Des. Discov. 2024, 21 (18), e15701808353391, 4148–4160. https://doi.org/10.2174/0115701808353391241106042408
  26. 26. Rodríguez P.N., Ghashghaei O., Bagán A., Escolano C. R. Biomedicines. 2022, 10 (7), 1488 (1–18), https://doi.org/10.3390/biomedicines10071488
  27. 27. Patel D.B., Rajani P.D., Rajani S.D, Patel H.D. J. Heterocycl. Chem. 2020, 57, 1524–1544, https://doi.org/10.1002/jhet.3848
  28. 28. Patel A., Patel S., Mehta M., Patel Y., Patel R., Shah D., Patel D., Shah U., Patel M., Patel S., Solanki N., Bambharoliya T., Patel S., Nagani A., Patel H., Vaghasiya J., Shah H., Prajapati B., Rathod M., Bhimani B., Patel R., Bhavsar V., Rakholiya B., Patel M., Patel P. Green Chem. Lett. Rev. 2022, 15 (2), 337–372. https://doi.org/10.1080/17518253.2022.2064194
  29. 29. T. Grover, Singh T., Vaja N., Maulikkumar, Curr. Org. Chem. 2023, 27, 1381–1392. https://doi.org/10.2174/0113852728268691231009063856
  30. 30. Aлексанян И.Л., Пивазян А.А., Aмбарцумян Л.П. Ученые записки Eреванского гос. университета хим. и биол. 2011, 1, 61–64. Доступен по http://www.old.ysu.am/files/NEW%20DERIVATIVES%20OF%20QUINOLINES%20ON%20THE%20BASE%20OF.pdf
  31. 31. Aleksanyan I.L., Hambardzumyan L.P. Russ. J. Org. Chem. 2024, 60 (6), 1022–1027. https://doi.org/10.1134/S107042802406006X
QR
Translate

Indexing

Scopus

Scopus

Scopus

Crossref

Scopus

Higher Attestation Commission

At the Ministry of Education and Science of the Russian Federation

Scopus

Scientific Electronic Library