Synthesis, Anticancer and Antibacterial Activities of Novel 2-Amino-4-phenylthiazole Derivatives Containing Amide Moiety
- Corresponding author: You Song, yousong206@aliyun.com
Citation:
Zhang Zhihu, Chen Yu, Chai Baoshan, Yang Xiaoman, Cai Xiaoyu, Cui Bo, You Song. Synthesis, Anticancer and Antibacterial Activities of Novel 2-Amino-4-phenylthiazole Derivatives Containing Amide Moiety[J]. Chinese Journal of Organic Chemistry,
;2017, 37(9): 2377-2384.
doi:
10.6023/cjoc201704023
(a) Heidorn, S. J.; Milagre, C.; Whittaker, S.; Nourry, A.; Niculescuduvas, I.; Dhomen, N.; Hussain, J.; Reisfilho, J. S.; Springer, C. J.; Pritchard, C. Cell 2010, 140, 209.
(b) Hatzivassiliou, G.; Song, K.; Yen, I.; Brandhuber, B. J.; Anderson, D. J.; Alvarado, R.; Ludlam, M. J.; Stokoe, D.; Gloor, S. L.; Vigers, G. Nature 2010, 464, 431.
Eisen, T.; Ahmad, T.; Flaherty, K. T.; Gore, M.; Kaye, S.; Marais, R.; Gibbens, I.; Hackett, S.; James, M.; Schuchter, L. M. Br. J. Cancer 2006, 95, 581.
doi: 10.1038/sj.bjc.6603291
(a) Wood, L. S. Community Oncol. 2006, 3, 558.
(b) Chu, E. Y. ; Wanat, K. A. ; Miller, C. J. ; Amaravadi, R. K. ; Fecher, L. A. ; Brose, M. S. ; McGettigan, S. ; Giles, L. R. ; Schuchter, L. M. ; Seykora, J. T. J. Am. Acad. Dermatol. 2012, 67, 1265.
(c) Autier, J. ; Escudier, B. ; Wechsler, J. ; Spatz, A. ; Robert, C. Arch. Dermatol. 2008, 144, 886.
(a) Wu, C.; Wang, M.; Tang, Q.; Luo, R.; Chen, L.; Zheng, P.; Zhu, W. Molecules 2015, 20, 19361.
(b) Yao, J.; Chen, J.; He, Z.; Sun, W.; Xu, W. Bioorg. Med. Chem. 2012, 20, 2923.
(c) Jung, M. H.; El-Gamal, M. I.; Abdel-Maksoud, M. S.; Sim, T.; Yoo, K. H.; Oh, C.-H. Bioorg. Med. Chem. Lett. 2012, 22, 4362.
(d) Jiao, Y.; Xin, B. T.; Zhang, Y.; Wu, J.; Lu, X.; Zheng, Y.; Tang, W.; Zhou, X. Eur. J. Med. Chem. 2015, 90, 170.
(e) Kong, X.; Yao, Z.; He, Z.; Xu, W.; Yao, J. MedChemComm 2015, 6, 867.
(f) Daydé-Cazals, B.; Fauvel, B.; Singer, M.; Feneyrolles, C.; Bestgen, B.; Gassiot, F.; Spenlinhauer, A.; Warnault, P.; Van Hijfte, N.; Borjini, N.; Chevé, G.; Yasri, A. J. Med. Chem. 2016, 59, 3886.
(g) Yao, J.; He, Z.; Chen, J.; Chen, D.; Sun, W.; Xu, W. Chin. J. Chem. 2012, 30, 2423.
(a) Gao, G. R.; Li, M. Y.; Lv, Y. C.; Cao, S. F.; Tong, L. J.; Wei, L. X.; Ding, J.; Xie, H.; Duan, W. H. Chin. Chem. Lett. 2016, 27, 200.
(b) Wu, Z.; Yan, M.; Hu, S. H.; Yu, Z. C.; Zhu, Y.; Cheng, Y. D.; Liu, H. C.; Zhang, Y. M.; Yao, S. H.; Tang, W. F.; Lu, T. Chin. Chem. Lett. 2014, 25, 351.
Liu, Y.; Gray, N. S. Nat. Chem. Biol. 2006, 2, 358.
doi: 10.1038/nchembio799
Das, D.; Sikdar, P.; Bairagi, M. Eur. J. Med. Chem. 2016, 109, 89.
doi: 10.1016/j.ejmech.2015.12.022
(a) Bharti, S. K.; Nath, G.; Tilak, R.; Singh, S. K. Eur. J. Med. Chem. 2010, 45, 651.
(b) Qin, Y. J.; Wang, P. F.; Makawana, J. A.; Wang, Z. C.; Wang, Z. N.; Yan, G.; Jiang, A. Q.; Zhu, H. L. Bioorg. Med. Chem. Lett. 2014, 24, 5279.
Coumar, M. S.; Chu, C. Y.; Lin, C. W.; Shiao, H. Y.; Ho, Y. L.; Reddy, R.; Lin, W. H.; Chen, C. H.; Peng, Y. H.; Leou, J. S.; Lien, T. W.; Huang, C. T.; Fang, M. Y.; Wu, S. H.; Wu, J. S.; Chittimalla, S. K.; Song, J. S.; Hsu, J. T.; Wu, S. Y.; Liao, C. C.; Chao, Y. S.; Hsieh, H. P. J. Med. Chem. 2010, 53, 4980.
doi: 10.1021/jm1000198
(a) Tseng, C. Magn. Reson. Chem. 1987, 25, 105.
(b) Bramley, S. E.; Dupplin, V.; Goberdhan, D. G.; Meakins, G. D. J. Chem. Soc., Perkin Trans 1. 1987, 639.
(c) Forlani, L.; Tocke, A. L.; Del Vecchio, E.; Lakhdar, S.; Goumont, R.; Terrier, F. J. Org. Chem. 2006, 71, 5527.
Metzger, J. V. In Chemistry of Heterocyclic Compounds, Vol. 34, Part 2, Ed.:Metzger, J. V., New York, 1979, p. 17.
Zhou, A.; Pittman, C. U. Tetrahedron Lett. 2005, 46, 3801.
doi: 10.1016/j.tetlet.2005.03.205
Yuan, M.; Liu, M.; Zhang, Y.; Yan, H.; Li, D.; Zhang, D.; Liu, H. Chin. J. Org. Chem. 2012, 32, 1746(in Chinese).
(a) Wermuth, C. G. Drug Discovery Today 2006, 11, 348.
(b) Martin, Y. C.; Kofron, J. L.; Traphagen, L. M. J. Med. Chem. 2002, 45, 4350.
(c) Vainio, M. J.; Puranen, J. S.; Johnson, M. S. J. Chem. Inf. Model. 2009, 49, 492.
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A: hydrogen bond acceptor; D: hydrogen bond donor; HRB: hinge-region binding; HM: hydrophobic motif
Reagents and conditions: (ⅰ) thiourea, ethanol, reflux, 5 h; (ⅱ) acetic anhydride, 130 ℃ for 24 h; (ⅲ) Fe, NH4Cl, ethanol/water, reflux; (ⅳ) CH2Cl2, Et3N, r.t.