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An Easy, Efficient and Improved Synthesis of Sertaconazole Nitrate

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Abstract

An easy, efficient and improved synthetic route has been developed for the synthesis of Sertaconazole (1-{2-[(7-chlorobenzo[b]thiophen-3-yl)methoxy]-2-(2,4-dichlorophenyl)ethyl}-1H-imidazole) employing multiple chemical transformation.

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References

  1. Carrillo-Munoz, A.J., Tur-Tur C., Giusiano G., Arias C.M., Eraso E., Jauregizar N., and Quindos, G., Expert Rev. Anti Infect. Ther., 2013, vol. 11, p. 347. doi https://doi.org/10.1586/eri.13.17

    Article  CAS  Google Scholar 

  2. Croxtall, J.D. and Plosker, G.L., Drugs, 2009, vol. 69, p. 339. doi https://doi.org/10.2165/00003495-200969030-00009

    Article  CAS  Google Scholar 

  3. Carrillo-Munoz, A.J., Tur-Tur, C., Cardenes, D.C., Estivill, D., and Giusiano, G., Antimicrob. Agents Chemother., 2011, vol. 55, p. 4420. doi https://doi.org/10.1128/AAC.00219-11

    Article  CAS  Google Scholar 

  4. Grossman, R. and Day, R., J. Am. Acad. Dermatol., 2005, vol. 52, p. 128. doi https://doi.org/10.1007/s00403-007-0744-y

    Google Scholar 

  5. Choudhary, S.V., Bisati, S., Singh, A.L., and Koley, S., Indian J. Dermatol., 2013, vol. 58, p. 457. doi https://doi.org/10.4103/0019-5154.119958

    Article  Google Scholar 

  6. Agut, J., Tarrida, N., Sacristan, A., and Ortiz, J.A., Meth. Find Exp. Clin. Pharmacol., 1996, vol. 18, p. 233.

    CAS  Google Scholar 

  7. Liebel, F., Lyte, P., Garay, M., Babad, J., and Southall, M.D., Arch. Dermatol. Res., 2006, vol. 298, p. 191. doi https://doi.org/10.1007/s00403-006-0679-8

    Article  CAS  Google Scholar 

  8. Sur, R., Babad, J.M., Garay, M., Liebel, F.T., and Southall, M.D., J. Invest. Dermatol., 2008, vol. 128, p. 336. doi https://doi.org/10.1038/sj.jid.5700972

    Article  CAS  Google Scholar 

  9. Jerajani, H.R., Janaki, C., Kumar, S., and Phiske, M., Indian J. Dermatol., 2013, vol. 58, p. 34. doi https://doi.org/10.4103/0019-5154.105284

    Article  Google Scholar 

  10. Chapman, N.B., Clarke, K., and Sawhney, S.N., J. Chem. Soc., 1968, p. 518. doi https://doi.org/10.1039/J39680000518

  11. Chapman, N.B., Clarke, K., and Iddon, B., J. Med. Chem., 1966, vol. 9, p. 819. doi https://doi.org/10.1021/jm00324a005

    Article  CAS  Google Scholar 

  12. Lawrence, P.A., and Marnett, J., J. Heterocycl. Chem., 1988, vol. 25, p. 1271. doi https://doi.org/10.1002/jhet.5570250445

    Article  Google Scholar 

  13. Raga, M., Palacin, C., Castello, J.M., Ortiz, A., Cuberes, M.R., and Moreno, M.M., Eur. J. Med. Chem., 1986, vol. 21, p. 329. doi https://doi.org/10.1021/jm00157a010

    CAS  Google Scholar 

  14. Raymundo, C.A., Teresa, H., Francisco, P., and Cristina, L., Org. Prep. Proc. Inter., 1992, vol. 24, p. 342. doi https://doi.org/10.1080/00304949209355898

    Article  Google Scholar 

  15. Peter, N., Gabor, P., and Anton, S., J. Med. Chem., 1991, vol. 34, p. 65. doi https://doi.org/10.1021/jm00105a008

    Article  Google Scholar 

  16. Dulcevscaia, G.M., Kravtsov, V.Ch., Macaev, F.Z., Duca, G.G., Stingachi, E.P., and Baca, S.G., Polyhedron, 2013, vol. 52, p. 106. doi https://doi.org/10.1016/j.poly.2012.10.040

    Article  CAS  Google Scholar 

  17. Alejandra, R.V., Davir, G.C., Carlos, G.R., Macario, M.R., Bertha, J.R., Eric, C.Y., and Aydee, F.B., Eur. J. Med. Chem., 2015, vol. 97, p. 275. doi https://doi.org/10.1016/j.ejmech.2015.04.047

    Article  Google Scholar 

  18. Lu, X., He, S., Li, Q., Yang, H., Jiang, X., Lin, H., Chen, Y., and Sun, H., Bioorg. Med.Chem., 2018, vol. 26, p. 1665. doi https://doi.org/10.1016/j.bmc.2018.02.014

    Article  CAS  Google Scholar 

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Acknowledgments

The authors wish to thank Dr. V.V.S.V Prasad and Dr. Dipankar Karmakar for their valuable support.

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Correspondence to S. Venkateswarlu Rayudu.

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Russian Text © The Author(s), 2019, published in Zhurnal Organicheskoi Khimii, 2019, Vol. 55, No. 8, pp. 1310.

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Venkateswarlu Rayudu, S., Kumar, P. An Easy, Efficient and Improved Synthesis of Sertaconazole Nitrate. Russ J Org Chem 55, 1212–1216 (2019). https://doi.org/10.1134/S1070428019080219

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  • DOI: https://doi.org/10.1134/S1070428019080219

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