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SYNTHESIS OF BROMINATED QUINOLINES

Yıl 2015, Cilt: 33 Sayı: 1, 8 - 15, 01.03.2015

Öz

In this study, bromination reactions of 1,2,3,4-tetrahydroquinoline by molecular bromine and aromatization reactions of brominated tetrahydroquinolines were reinvestigated. Optimal reaction conditions were established for 6-Bromo-1,2,3,4-tetrahydroquinoline (6-BrTHQ ) and 6,8-dibromo-1,2,3,4-tetrahydroquinoline (6,8-diBrTHQ). Improved yields and more shortened reaction times were described for the conversion of 6-BrTHQ and 6,8-diBrTHQ into 6-bromoquinoline and 6,8-dibromoquinoline.

Kaynakça

  • [1] Kirsch, R., Kleim, J. P., Ries, G., Rosenstock, B., Roesner, M., Winkler, I. DE Patent 19,613,591, (1997).
  • [2] Srivastava, S. K., Chauhan, P. M. S., Bhaduri, A. P., Fatima, N., Chatterjee, R. J. Med. Chem., 43, 2275, (2000).
  • [3] Desai, P. K., Desai, P., Machhi, D., Desai, C. M., Patel, D. Indian J. Chem. Sect. B, 35(B), 871, (1996).
  • [4] Muscia, G. C., Bollini, M., Carnevale, J. P., Bruno, A. M., Asis, S. E. Tetrahedron Lett., 47, 8811, (2006).
  • [5] Agarwal, A. K., Jenekhe, S. A. Macromolecules, 24, 6806 (1991).
  • [6] Zhang, X., Shetty, A. S., Jenekhe, S. A. Macromolecules, 32, 7422 (1999).
  • [7] Zhang, N., Wu, B.,Powell, D., Wissner, A., Floyd, M.B., Kovacs, E.D., Toral-Barza, L., Kohler, C. Bioorg. Med. Chem. Lett., 10, 2825-2828, (2000).
  • [8] Jenekhe, S. A., Lu, L., Alam, M. M. Macromolecules, 34, 7315. (2001).
  • [9] Solomon, V. R., Lee, H. Eur. J. Pharmacol., 625, 220, (2009).
  • [10] Boschelli, D.H., Wang, D.Y., Ye, F., Wu, B., Zhang, N., Dutia, M., Powell D. W., Wissner, A., Arndt, K., Weber, J.M., Boschelli, J. Med. Chem., 44, 822-833, (2001).
  • [11] Company of a Chemistry Partner of Drug Discovery “BioBloks inc.”, 2002, San Diego, CA, USA. http://www.bioblocks.com/quinolines.html, [Erişim tarihi; 26 Şubat 2014].
  • [12] Şahin, A., Çakmak, O., Demirtaş, İ., Ökten, S., Tutar, A., Tetrahedron, 64 (43), 10068-10074 (2008).
  • [13] Ökten, S, Çakmak O, Erenler R, Tekin Ş, Yüce Ö., Turk. J. Chem. 37, 896-908 (2013).
Yıl 2015, Cilt: 33 Sayı: 1, 8 - 15, 01.03.2015

Öz

Kaynakça

  • [1] Kirsch, R., Kleim, J. P., Ries, G., Rosenstock, B., Roesner, M., Winkler, I. DE Patent 19,613,591, (1997).
  • [2] Srivastava, S. K., Chauhan, P. M. S., Bhaduri, A. P., Fatima, N., Chatterjee, R. J. Med. Chem., 43, 2275, (2000).
  • [3] Desai, P. K., Desai, P., Machhi, D., Desai, C. M., Patel, D. Indian J. Chem. Sect. B, 35(B), 871, (1996).
  • [4] Muscia, G. C., Bollini, M., Carnevale, J. P., Bruno, A. M., Asis, S. E. Tetrahedron Lett., 47, 8811, (2006).
  • [5] Agarwal, A. K., Jenekhe, S. A. Macromolecules, 24, 6806 (1991).
  • [6] Zhang, X., Shetty, A. S., Jenekhe, S. A. Macromolecules, 32, 7422 (1999).
  • [7] Zhang, N., Wu, B.,Powell, D., Wissner, A., Floyd, M.B., Kovacs, E.D., Toral-Barza, L., Kohler, C. Bioorg. Med. Chem. Lett., 10, 2825-2828, (2000).
  • [8] Jenekhe, S. A., Lu, L., Alam, M. M. Macromolecules, 34, 7315. (2001).
  • [9] Solomon, V. R., Lee, H. Eur. J. Pharmacol., 625, 220, (2009).
  • [10] Boschelli, D.H., Wang, D.Y., Ye, F., Wu, B., Zhang, N., Dutia, M., Powell D. W., Wissner, A., Arndt, K., Weber, J.M., Boschelli, J. Med. Chem., 44, 822-833, (2001).
  • [11] Company of a Chemistry Partner of Drug Discovery “BioBloks inc.”, 2002, San Diego, CA, USA. http://www.bioblocks.com/quinolines.html, [Erişim tarihi; 26 Şubat 2014].
  • [12] Şahin, A., Çakmak, O., Demirtaş, İ., Ökten, S., Tutar, A., Tetrahedron, 64 (43), 10068-10074 (2008).
  • [13] Ökten, S, Çakmak O, Erenler R, Tekin Ş, Yüce Ö., Turk. J. Chem. 37, 896-908 (2013).
Toplam 13 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Bölüm Research Articles
Yazarlar

Salih Ökten Bu kişi benim

Dilek Eyigün Bu kişi benim

Osman Çakmak Bu kişi benim

Yayımlanma Tarihi 1 Mart 2015
Gönderilme Tarihi 19 Temmuz 2014
Yayımlandığı Sayı Yıl 2015 Cilt: 33 Sayı: 1

Kaynak Göster

Vancouver Ökten S, Eyigün D, Çakmak O. SYNTHESIS OF BROMINATED QUINOLINES. SIGMA. 2015;33(1):8-15.

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