Synthesis of new disulfonamides from different substituted diamino pyridines

Main Article Content

Hossein Behmadi
Seyed Mahdi Saadati
Mina Roshani
Mousa Ghaemy

Abstract

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.

Metrics

Metrics Loading ...

Article Details

How to Cite
Behmadi, H., Saadati, S. M., Roshani, M., & Ghaemy, M. (2009). Synthesis of new disulfonamides from different substituted diamino pyridines. Eclética Química, 34(3), 27–31. https://doi.org/10.26850/1678-4618eqj.v34.3.2009.p27-31
Section
Original articles

References

(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.