Synthesis and characterization of some novel 7-(aryl)-3-phenyl-6-(1H-tetrazol-5-yl)-5H-thiazolo[3,2-a]pyrimidin-5-one derivatives
Tóm tắt
A series of novel tetrazole derivatives containing fused thiazolo[3,2-a]pyrimidines were synthesized in a one-pot three-component reaction of 7-(aryl)-5-oxo-3-phenyl-5H-thiazolo[3,2-a]pyrimidine-6-carbonitriles with sodium azide and ammonium chloride.
Tài liệu tham khảo
Khalifa, N.M., Al-Omar, M.A., Amr, A.E., Baiuomy, A.R., and Fawzy R.A., Russ. J. Bioorg. Chem., 2015, vol. 41, no. 2, p. 192. doi 10.1134/S1068162015020090
Vergush, A.P., Emma, A.G., Roza, S.S., Rafael, A.T., Armen, G.A., and Aleksandr, P.Y., J. Chem., 2017, vol. 2017, p. 1. doi org/10.1155/2017/8180913
Dong, C., Zhi-Hua, Z., Yu, C., Xin-Jia, Y., Shi-Ti, Z., Liang-Jing, Z., Li-Hong, M., Fang, L., and Bing-Jie, F., Med. Chem. Res., 2016, vol. 25(2), p. 292. doi 10.1007/s00044-015-1481-y
Samia, G.A., Mostafa, A.H., Salah, A.A., and Mahrous, A.A., Saudi Pharm. J., 2016, vol. 24, p. 119. doi org/10.1016/j.jsps.2013.12.016
Suresh, L., Sagar, P., Poornachandra, Y., Ganesh, C., Babu, J., and Chandramouli, V., Bioorg. Med. Chem., 2016, vol. 24(16), p. 3808. doi 10.1016/j.bmc.2016.06.025
Dong, C., Zhi-Hua, Z., Yu, C., Xin-Jia, Y., Liang-Jing, Z., Ya-Xin, W., and Xue-Qi, L., Molecules, 2015, vol. 20, p. 16419. doi 10.3390/molecules200916419
Alireza, B., Vikneswaran, M., Hasnah, O., Raju, S.K., Yalda, K., Alysha, H., and Richard, B.P., Bioorg. Med. Chem., 2014, vol. 22, p. 906. doi org/10.1016/j.bmc.2013.11.020
Abu-Hashem, A.A., Youssef, M.M., and Hussein, H.A.R., J. Chin. Chem. Soc., 2011, vol. 58(1), p. 41. doi 10.1002/jccs.201190056
Seerat, F., Anindra, S., Reshu, S., Rajkamal, T., Sanjeev, K.S., Swaroop, K.P., Renu, T., and Rama, P.T., Eur. J. Med. Chem., 2012, vol. 55, p. 195. doi org/10.1016/j.ejmech.2012.07.018
Lingaiah, N., Satheeshvarma, V., Rajashaker, B., and Ganesh, K., Eur. J. Med. Chem., 2013, vol. 69, p. 817. doi org/10.1016/j.ejmech.2013.08.024
El Nezhawy, A.O., Ramla, M.M., Khalifa, N.M., and Abdulla, M.M., Monatsh Chem., 2009, vol. 140, p. 531. doi 10.1007/s00706-008-0085-3
Gein, V.L., Zamaraeva, T.M., Panova, O.S., Belonogova, V.D., and Nasakin, O.E., Russ. J. Gen. Chem., 2016, vol. 86, no. 2, p. 417. doi 10.1134/S1070363216020389
Yeung, K.S., Qiu, Z., Yang, Z., Zadjura, L., D’Arienzo, C.J., Browning, M.R., Hansel, S., Huang, X.S., Eggers, B.J., Riccardi, K., Lin, P.F., Meanwell, N.A., and Kadow, J.F., Bioorg. Med. Chem. Lett., 2013, vol. 23, p. 209. doi 10.1016/j.bmcl.2012.10.125
Arshad, M., Bhat, A.R., Pokharel, S., Kim, J.E., Lee, E.J., Athar, F., and Choi, I., Eur. J. Med. Chem., 2014, vol. 71, p. 229. doi org/10.1016/j.ejmech.2013.11.008
Romagnoli, R., Baraldi, P.G., Salvador, M.K., Preti, D., Aghazadeh, T.M., Brancale, A., Fu, X.H., Li, J., Zhang, S.Z., Hamel, E., Bortolozzi, R., Basso, G., and Viola, G., J. Med. Chem., 2012, vol. 55, p. 475. doi 10.1021jm2013979