Collect. Czech. Chem. Commun.
2011, 76, 1909-1915
https://doi.org/10.1135/cccc2011129
Published online 2012-01-26 11:12:14
1,3-Dibromo-5,5-dimethylhydantoin catalyzed one-pot synthesis of 2-arylbenzothiazoles
Xiaojuan Yanga,* and Jinying Liangb
a College of Chemistry and Chemical Engineering, Xinxiang University, Xinxiang, Henan 453003, China
b School of Pharmacy, Xinxiang Medical University, Xinxiang, Henan 453003, China
References
1. R. D., Angel R. G.., Jacobs G. A., Maurer B. V., Narayanan V. L., Cruthers L. R., Szanto J.: J. Med. Chem. 1982, 25, 969.
<https://doi.org/10.1021/jm00350a017>
2. A. N., Sakai S., El-Gendy M. A., Omar N., Farag H. H.: Chem. Pharm. Bull. 1989, 37, 2971.
<https://doi.org/10.1248/cpb.37.2971>
3a. D. F., Bradshaw T. D., Wrigley S., McCall C. J., Lelieveld P., Fichtner I., Stevens M. F.: J. Med. Chem. 1996, 39, 3375.
<https://doi.org/10.1021/jm9600959>
3b. G., Bradshaw T. D., Diana P., Seaton A., Shi D. F., Westwell A. D., Stevens M. F.: Bioorg. Med. Chem. Lett. 2000, 10, 513.
<https://doi.org/10.1016/S0960-894X(00)00027-5>
3c. I., Chua M. S., Browne H. L., Trapani V., Bradshaw T. D., Westwell A. D., Stevens M. F.: J. Med. Chem. 2001, 44, 1446.
<https://doi.org/10.1021/jm001104n>
3d. L., Kralj M., Suman L., Stojkovic R., Tralic-Kulenovic V., Karminski-Zamola G..: Bioorg. Med. Chem. Lett. 2010, 18, 1038.
4a. R. S., Bahekar R. H., Khedekar P. B., Bhusari K. P., Rao A. R. R.: Arch. Pharm. 2002, 335, 381.
<https://doi.org/10.1002/1521-4184(200211)335:8<381::AID-ARDP381>3.0.CO;2-S>
4b. N. D., Bhusari K. P.: Eur. J. Med. Chem. 2010, 45, 149.
<https://doi.org/10.1016/j.ejmech.2009.09.037>
5. M., Noolvi M., Sankangoud R., Maddi V., Gadad A., Nargund L. V. G.: Arch. Pharm. 2010, 343, 353.
<https://doi.org/10.1002/ardp.200900260>
6. I., Grdisa M., Mrvos-Sermek D., Cetina M., Tralic-Kulenovic V., Pavelic K., Karminski-Zamola G.: Farmaco 2004, 59, 297.
<https://doi.org/10.1016/j.farmac.2004.01.008>
7. T., Srivastava V. K., Saxena K. K., Goel S. L., Kumar A.: Arch. Pharm. 2006, 339, 466.
<https://doi.org/10.1002/ardp.200500265>
8. R. D., Angel R. G., Jacobs G. A., Maurer B. V., Narayanan V. L., Cruthers L. R., Szanto J.: J. Med. Chem. 1982, 25, 969.
<https://doi.org/10.1021/jm00350a017>
9. L., Tralic-Kulenovic V., Kitson R. P., Karminski-Zamola G.: Monatsh. Chem. 2006, 137, 1571.
<https://doi.org/10.1007/s00706-006-0546-5>
10. G., de Saqui-Sannes G., Younes S., Bellan J., Payard M., Tisne-Versailles J.: Farmaco 1990, 45, 945.
11. S.-J., Park H. J., Lee S. K., Kim S. W., Han G., Choo H.-Y.: Bioorg. Med. Chem. 2006, 14, 1229.
<https://doi.org/10.1016/j.bmc.2005.09.051>
12. A. A., Westwell A. D.: Curr. Med. Chem. 2009, 16, 2430.
<https://doi.org/10.2174/092986709788682137>
13. B.: Collect. Czech. Chem. Commun. 2011, 76, 27.
<https://doi.org/10.1135/cccc2010111>
14. B., Salehabadi H., Moghaddam M. K.: Acta Chim. Slov. 2010, 57, 741.
15. H.-L., Cheng T.-X., Chen J.-X.: Appl. Organomet. Chem. 2011, 25, 238.
<https://doi.org/10.1002/aoc.1793>
16. A., Fazlaeli R., Fazaeli N., Mssah A. R., Javaherian-Naghash H., Alizadeh M., Emami G.: Heteroatom Chem. 2009, 20, 202.
<https://doi.org/10.1002/hc.20534>
17. D., Maleki B., Setayeshnazar M.: Phosphorus, Sulfur Silicon Relat. Elem. 2009, 184, 2097.
<https://doi.org/10.1080/10426500802423933>
18. T., Yamada S., Yamazaki Y., Tanaka H.: Synth. Commun. 2009, 39, 2982.
<https://doi.org/10.1080/00397910902730838>
19. F., Mekheimer R. R., Sadek K. U.: Molecules 2008, 13, 2908.
<https://doi.org/10.3390/molecules13112908>
20. K., Khodaei M. M., Naali F.: Synlett 2009, 569.
<https://doi.org/10.1055/s-0028-1087911>
21. C., Datta A.: J. Heterocycl. Chem. 2009, 46, 91.
<https://doi.org/10.1002/jhet.9>
22. H. L., Chen J. X., Liu M. C., Zhu D. J., Ding J. C., Wu H. Y.: Chem. Lett. 2009, 38, 170.
<https://doi.org/10.1246/cl.2009.170>
23. R., Aliyan H.: Appl. Catal., A 2009, 353, 74.
24. M. B., Allam S. K., Mandha A., Chandramouli G. V. P.: ARKIVOC 2008, xv, 42.
25. H., Omid A.: Synth. Commun. 2009, 39, 860.
<https://doi.org/10.1080/00397910802431214>
26. M., Tamaru Y., Aoyama T.: Synth. Commun. 2004, 34, 3029.
<https://doi.org/10.1081/SCC-200026663>
27. Y., Wang G. Y., Wang J. Y., Jacquline L.: Chem. Lett. 2006, 35, 460.
<https://doi.org/10.1246/cl.2006.460>
28. L., Tralic-Kulenovic V., Boykin D. W., Karminski-Zamola G.: Molecules 2003, 8, 342.
<https://doi.org/10.3390/80300342>
29. P. I., Moisan L.: Angew. Chem., Int. Ed. 2004, 43, 5138.
<https://doi.org/10.1002/anie.200400650>
30a. D., Bosra H. G., Tajbaksh M.: J. Heterocycl. Chem. 2007, 44, 467.
<https://doi.org/10.1002/jhet.5570440231>
30b. D., Maleki B., Mohammadi K.: Heterocycles 2007, 71, 683.
<https://doi.org/10.3987/COM-06-10961>
30c. S. K., Misra A. K.: Carbohydr. Res. 2005, 340, 497.
<https://doi.org/10.1016/j.carres.2004.12.002>
31a. M., Nakahara Y., Yoshioka H.: J. Chem. Soc., Chem. Commun. 1989, 1881.
<https://doi.org/10.1039/c39890001881>
31b. C., Haudrechy A., Langlois Y.: Tetrahedron Lett. 1997, 38, 4415.
<https://doi.org/10.1016/S0040-4039(97)00943-X>

