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.
Similar content being viewed by others
References
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
Croxtall, J.D. and Plosker, G.L., Drugs, 2009, vol. 69, p. 339. doi https://doi.org/10.2165/00003495-200969030-00009
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
Grossman, R. and Day, R., J. Am. Acad. Dermatol., 2005, vol. 52, p. 128. doi https://doi.org/10.1007/s00403-007-0744-y
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
Agut, J., Tarrida, N., Sacristan, A., and Ortiz, J.A., Meth. Find Exp. Clin. Pharmacol., 1996, vol. 18, p. 233.
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
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
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
Chapman, N.B., Clarke, K., and Sawhney, S.N., J. Chem. Soc., 1968, p. 518. doi https://doi.org/10.1039/J39680000518
Chapman, N.B., Clarke, K., and Iddon, B., J. Med. Chem., 1966, vol. 9, p. 819. doi https://doi.org/10.1021/jm00324a005
Lawrence, P.A., and Marnett, J., J. Heterocycl. Chem., 1988, vol. 25, p. 1271. doi https://doi.org/10.1002/jhet.5570250445
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
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
Peter, N., Gabor, P., and Anton, S., J. Med. Chem., 1991, vol. 34, p. 65. doi https://doi.org/10.1021/jm00105a008
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
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
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
Acknowledgments
The authors wish to thank Dr. V.V.S.V Prasad and Dr. Dipankar Karmakar for their valuable support.
Author information
Authors and Affiliations
Corresponding author
Additional information
Russian Text © The Author(s), 2019, published in Zhurnal Organicheskoi Khimii, 2019, Vol. 55, No. 8, pp. 1310.
Rights and permissions
About this article
Cite this article
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
Received:
Revised:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1134/S1070428019080219