Bulletin of the Korean Chemical Society

  • 제32권7호
  • /
  • Pages.2183-2186
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  • 2011
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  • 0253-2964(pISSN)
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  • 1229-5949(eISSN)
대한화학회 (Korean Chemical Society)
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Synthesis of Some Pyrimido[4,5-b]quinoline Derivatives

  • Marjani, Ahmad Poursattar (Department of Chemistry, Faculty of Science, Urmia University) ;
  • Khalafy, Jabbar (Department of Chemistry, Faculty of Science, Urmia University) ;
  • Ebrahimlo, Ali Reza Molla (Department of Chemistry, Islamic Azad University) ;
  • Prager, Rolf.H. (School of Chemical and Physical Sciences, Flinders University)
  • 투고 : 2011.04.16
  • 심사 : 2011.05.09
  • 발행 : 2011.07.20
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초록

A series of pyrimidoquinoline derivatives was synthesized in good yield and short reaction times by reaction of 3-arylaminoisoxazol-5(2H)-ones with derivatives of 2-chloro-3-formylquinoline in toluene under reflux conditions.

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참고문헌

  1. El-Sabbagh, H. I.; Abadi, A. H.; Al-Khawad, I. E.; Al-Rashood, K. A. Arch. Pharm. Pharm. Med. Chem. 1990, 333, 19.
  2. Bol, S. A.; Horibeck, J.; Markovic, J.; de Boer, J. G.; Turesky, R. J.; Constable, A. Carcinogenesis 2000, 21, 1. https://doi.org/10.1093/carcin/21.1.1
  3. El-Sayed, O. A.; El-Semary, M.; Khalid, M. A. Alex. J. Pharm. Sci. 1996, 10, 43.
  4. Althuis, T. H.; Moore, P. F.; Hess, H. J. J. Med. Chem. 1979, 22, 44. https://doi.org/10.1021/jm00187a011
  5. Nargund, L. V. G.; Badiger, V. V.; Yarnal, S. M. J. Pharm. Sci. 1992, 81, 365. https://doi.org/10.1002/jps.2600810416
  6. El-Sayed, O. A.; El-Baih, F. M. E.; El-Aqeel, Sh. I.; Al Bassam, B. A.; Hussein, M. E. Boll. Chem. Farmac. 2002, 141, 461.
  7. Petal, N. C.; Mehta, A. G. Asian J. Chem. 2001, 13, 1385.
  8. Taylos, E. C.; Kalenda, N. J. Org. Chem. 1956, 78, 5108.
  9. Poursattar Marjani, A.; Khalafy, J.; Molla Ebrahimlo, A. R. Synth. Commun. 2011, 41. 2475. https://doi.org/10.1080/00397911.2010.505701
  10. Khalafy, J.; Poursattar Marjani, A.; Molla Ebrahimlo, A. R. J. Braz. Chem. Soc. 2006, 17, 570. https://doi.org/10.1590/S0103-50532006000300021
  11. Khalafy, J.; Molla Ebrahimlo, A. R.; Eisavi, R.; Akbari Dilmaghani, K. ARKIVOC. 2005, xiv, 59.
  12. Meth-Cohn, O.; Narine, B.; Tarnowski, B. J. Chem. Soc. Perkin Trans. 1 1981, 1520.

피인용 문헌

  1. CuO Nanoparticles as an Efficient and Reusable Catalyst for the One-pot Friedlander Quinoline Synthesis vol.32, pp.11, 2011, https://doi.org/10.5012/bkcs.2011.32.11.3853
  2. ChemInform Abstract: Synthesis of Some Pyrimido[4,5-b]quinoline Derivatives. vol.42, pp.51, 2011, https://doi.org/10.1002/chin.201151157
  3. A novel synthesis of imidazo[1,2-a]quinoxalines vol.48, pp.6, 2012, https://doi.org/10.1007/s10593-012-1079-y
  4. ]quinoline-9-yl(aryl)methanone Derivatives vol.54, pp.1, 2017, https://doi.org/10.1002/jhet.2637
  5. ]pyridine-10,12-diones pp.0022152X, 2017, https://doi.org/10.1002/jhet.2949
  6. Recent Advances on Diversity Oriented Heterocycle Synthesis of Fused Quinolines and Its Biological Evaluation vol.41, pp.10, 2011, https://doi.org/10.1080/10406638.2019.1710856