Skip to main content
Log in

Synthesis and antimicrobial studies of new pyridine derivatives

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

2-(p-Acetylaminobenzenesulfonylamido)-substituted benzothiazoles were prepared from 2-amino-substituted benzothiazoles and p-acetamidobenzenesulfonyl chloride using a mixture of pyridine and Ac2O, which formed an electrophilic N-acetyl- pyridinium complex facilitating condensation to give the desired products by removal of HCl. 2-[4-(Substituted benzothiazol-2-yl)aminosulfonylanilino]pyridine-3-carboxylic acids (synthesized from 2-chloropyridine-3-carboxylic acid and the corresponding substituted 2-(p-aminobenzenesulfonylamido)benzothiazole in 2-ethoxyethanol using Cu-powder and K2CO3) were then converted to acid chlorides, which on further reaction with piperazine and 4-methoxyphenylpiperazine yielded the corresponding 2-[4-(substituted benzothiazol-2-yl)amino-sulfonyl]anilino-3-(piperazinocarbonyl) pyridine and 2-[4-(substituted benzothiazol-2-yl)amino-sulfonyl]anilino-3-[(4-methoxyphenyl)piperazin-1-yl-carbonyl]pyridine. The structures of the new compounds have been established on the basis of their elemental analyses as well as IR, 1H NMR, and mass-spectral data. All the compounds have been screened for antimicrobial activity and found to possess considerable antibacterial activity.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Similar content being viewed by others

References

  1. P. D. Bouzard, P. D. Cesare, C. Dussy, J. P. Jacquet, and A. Jaegly, J. Heterocycl. Chem., 29, 985 (1992).

    Article  Google Scholar 

  2. O. Tabarrini, G. Manfroni, A. Fravolini, V. Cecchetti, S. Stefano, E. D. Clereq, J. Rozenski, B. Canard, H. Dutarte, J. Paeshuyse, and J. Neyts, J. Med. Chem., 49, 2621 (2006).

    Article  CAS  Google Scholar 

  3. S. X. Cai, N. S. Jia, J. Herich, J. Guastella, S. Reddy, B. Tseng, J. Drewe, and S. Kasibhatla, J. Med. Chem., 46, 2474 (2003).

    Article  CAS  Google Scholar 

  4. J. A. Lowe, Austrian Pat. 388378; Chem. Abstr., 112, 21008 (1990).

    Google Scholar 

  5. B. M. Gurupadaiah, E. Jayachandran, B. ShivaKumar, A. N. Nagappa, and L. V. G. Nargund, Indian J. Heterocycl. Chem., 7, 213 (1998).

    CAS  Google Scholar 

  6. P. Gopkumar, B. Shivakumar, E. Jayachandran, A. N. Nagappa, L. V. G. Nargund, and B. M. Gurupadaiah, Indian J. Heterocycl. Chem., 11, 39 (2001).

    CAS  Google Scholar 

  7. B. G. Khadse and S. R. Sengupta, Indian J. Chem., 32B, 407 (1993).

    Google Scholar 

  8. S. I. Ratzne, D. Bazsing, I. Jakozi, L. G. Kovanyine, G. Blasko, G. Siming, I. Gacsalyi, and E. Schmidt, PCT Int. Appl. WO 97 44334 (1997); Chem. Abstr., 128, 34786 (1998).

    Google Scholar 

  9. R. C. Trpathi, P. R. Dua, R. C. Srimal, and A. K. Saxena, Indian J. Chem., 34B, 116 (1995).

    Google Scholar 

  10. K. Araki, T. Kuroda, S. Uemori, A. Morigucsi, Y. Ikeda, F. Hirayama, Y. Yokoyama, E. Iwao, and T. Yakushiji, J. Med. Chem., 36, 1356 (1993).

    Article  CAS  Google Scholar 

  11. S. Seshadri, N. M. Sanghavi, K. V. Naik, S. K. Tawate, M. N. Trivedi, and M. A. Fruitwala, Indian J. Chem., 32B, 688 (1993).

    CAS  Google Scholar 

  12. N. B. Patel and S. N. Agravat, Indian J. Heterocycl. Chem., 15, 395 (2006).

    CAS  Google Scholar 

  13. N. B. Patel and S. N. Agravat, Oriental J. Chem., 22, 333 (2006).

    CAS  Google Scholar 

  14. N. B. Patel and S. N. Agravat, J. Saudi Chem. Soc., 10, 373 (2006).

    CAS  Google Scholar 

  15. N. B. Patel and P. R. Bhagat, J. Indian Coun. Chem., 18, 56 (2001).

    CAS  Google Scholar 

  16. A. L. Barry, The Antimicrobial Susceptibility Test; Principles and Practices, Lea and Febiger, Philadelphia, Pa, USA, 1976.

    Google Scholar 

  17. S. R. Bhusare, R. P. Pawar, and Y. B. Vibhute, Indian J. Heterocycl. Chem., 11, 79 (2001).

    CAS  Google Scholar 

  18. A. I. Vogel, Small Scale Preparations, CBS Publ., Distributors, Delhi, 2nd ed., 1998, Pt I, p. 366.

    Google Scholar 

  19. J. A. Lowe III, R. L. Archer, D. S. Chapin, J. B. Cheng, D. Helweg, J. L. Johnson, B. K. Koe, L. A. Lebel, P. F. Moore, J. A. Nielsen, L. L. Russo, and J. T. Shirley, J. Med. Chem., 34, 624 (1991).

    Article  CAS  Google Scholar 

  20. A. I. Vogel, Small Scale Preparations, CBS Publ., Distributors, Delhi, 2nd ed., 1998, Pt II, p. 209.

    Google Scholar 

  21. M. Vlassa, J. Barbe, and P. Brounat, Indian J. Heterocycl. Chem., 7, 149 (1997).

    CAS  Google Scholar 

  22. A. I. Vogel, Small Scale Preparations, CBS Publ., Distributors, Delhi, 2nd ed., 1998, Pt I, p. 345.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to N. B. Patel.

Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1672–1683, November, 2009.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Patel, N.B., Agravat, S.N. Synthesis and antimicrobial studies of new pyridine derivatives. Chem Heterocycl Comp 45, 1343–1353 (2009). https://doi.org/10.1007/s10593-010-0432-2

Download citation

  • Received:

  • Revised:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10593-010-0432-2

Keywords

Navigation