Resumo
A series of novel disulfonamide derivatives were synthesized and characterized by FT-IR, 1H NMR and MS techniques. In order to prepare new disulfonamides, at first we synthesized new diamines containing a pyridine ring. Then, they have been reacted with sulfonyl chlorides to give corresponding disulfonamides.Referências
(a) C. T. Supuran, A. Casini and A. Scozzafava, Med. Res. Rev., 5 (2003) 535.
(b) A. Scozzafava, T. Owa, A. Mastrolorenzo and C. T. Supuran, Curr. Med. Chem., 10 (2003) 925.
A. Kleemann, J. Engel, B. Kutscher, D. Reichert, Eds; Pharmaceutical Substances, Syntheses, Patents, Applications, (Thieme, Stuttgart, 1999).
(a) W. R. Roush, S. L. Gwaltney, J. Cheng, K. A. Scheidt, J. H. McKerrow, E. Hansell, J. Am. Chem. Soc., 120 (1998) 10994.
(b) W. R. Roush, J.Cheng, B. Knapp- Reed, A. Alvarez-Hernandez, J. H. McKerrow, E. Hansell, J. C. Engel, Bioorg. Med. Chem. Lett., 11 (2001) 2759.
R. Pandya, T. Murashima, L. Tedeschi, A. G. M. Barrett, J. Org. Chem., 68 (2003) 8274.
N. Özbek, H. Katırcıoğlu, N. Karacan, T. Baykal, Bioorg. Med. Chem., 15 (2007) 5105.
J. F. O’Connel, H. Rapoport, J. Org. Chem., 57 (1992) 4775.
C. Hansch, P. G. Sammes, J. B. Taylor, Comprehensive Medicinal Chemistry, (Pergamon Press, Oxford, 1990) Vol. 2, Chapter 7.1.
L. De Luca, G. Giacomelli, J. Org. Chem., 73 (2008) 3967.
S. Caddick, J. D. Wilden, H. D. Bush, S. N. Wadman, D. N. Judd, Org. Lett., 4 (2002) 2549.
A. R. Katritzky, V. Rodriguez-Garcia, S. K. Nair, J. Org. Chem., 69 (2004) 1849.
S. W. Wright, K. N. Hallstrom, J. Org. Chem., 71 (2006) 1080.
S. Caddick, J. D. Wilden, D. B. Judd, J. Am. Chem. Soc., 126 (2004) 1024.
A. Shaabani, E. Soleimani, A. H. Rezayan, Tetrahedron Lett., 48 (2007) 2185.
F. Kröhnke, W. Zecher, Angew. Chem., Int. Ed., 1 (1962) 626.
F. Kröhnke, Synthesis, (1976) 1.
(a) K. T. Potts, M. J. Cipullo, P. Ralli, G. Theodoridis, J. Am. Chem. Soc., 103 (1981) 3584.
(b) K. T. Potts, M. J. Cipullo, P. Ralli, G. Theodoridis, J. Am. Chem. Soc. 103 (1981) 3585.
T. Kobayashi, H. Kakiuchi, H. Kato, Bull. Chem. Soc. Jpn., 64 (1991) 392.
F. Palacios, A. M. O. de Retana, J. Oyarzabal, Tetrahedron Lett., 37 (1996) 4577.
G. W. V. Cave, C. L. Raston, Chem. Commun., (2000) 2199.
S. Tu, T. Li, F. Shi, F. Fang, S. Zhu, X. Wei, Z. Zong, Chem. Lett., 34 (2005) 732.
B. Tamami, H. Yeganeh, Polymer, 42 (2001) 415.

Este trabalho está licenciado sob uma licença Creative Commons Attribution 4.0 International License.
Copyright (c) 2018 Eclética Química



