Citation: Zheng Yu-Tao, Zhang Teng-Teng, Wang Pei-Yi, Wu Zhi-Bing, Zhou Lei, Ye Yi-Qiang, Zhou Xiang, He Ming, Yang Song. Synthesis and bioactivities of novel 2-(thioether/sulfone)-5-pyrazolyl-1, 3, 4-oxadiazole derivatives[J]. Chinese Chemical Letters, ;2017, 28(2): 253-256. doi: 10.1016/j.cclet.2016.06.055 shu

Synthesis and bioactivities of novel 2-(thioether/sulfone)-5-pyrazolyl-1, 3, 4-oxadiazole derivatives

  • Corresponding author: Yang Song, jhzx.msm@gmail.com
  • 1These authors contributed equally to this work
  • Received Date: 28 April 2016
    Revised Date: 26 June 2016
    Accepted Date: 30 June 2016
    Available Online: 9 February 2016

Figures(2)

  • By introducing the pyrazole moiety into the 5-position of 1, 3, 4-oxadiazole, a series of novel 2-(thioether/sulfone)-5-pyrazolyl-1, 3, 4-oxadiazole derivatives were synthesized. Preliminary bioassays suggested that target compounds exhibited appreciable activity against pathogenic bacteria Xanthomonas oryzae pv. oryzae (Xoo) and five phytopathogenic fungi in vitro. Among them, the half-maximal effective concentration (EC50) values of 6c, 7a, 7b and 7c against Xoo were within 16.6 μg/mL and 65.7 μg/mL, which were better than those of commercial agricultural antibacterial bismerthiazol (92.6 μg/mL) and thiodiazole copper (121.8 μg/mL). While compounds 7a, 7b, and 7c exerted comprehensive antifungal activity toward five plant fungi, which were comparable with that of hymexazol. The results demonstrated that this kind of compounds can be further studied and developed as promising antifungal and antibacterial agents.
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    1. [1]

      N. Kahriman, B. Yayli, A. Aktas, Z. Iske _fiyeli, F.S. Beris, N. Yayli. Synthesis, antibacterial and antioxidant activities of new 1-alkyl-4-(1-alkyl-4-oxo-1, 4-dihydroquinolin-2-yl) pyridinium bromides[J]. Eur. J. Med. Chem., 2013,69:348-355. doi: 10.1016/j.ejmech.2013.08.050

    2. [2]

      X. Zuo, N. Mi, Z.J. Fan, Q.X. Zheng, H.K. Zhang, H. Wang, Z.K. Yang. Synthesis of 4-methyl-1, 2, 3-thiadiazole derivatives via ugi reaction and their biological activities[J]. J. Agric. Food Chem., 2010,58:2755-2762. doi: 10.1021/jf902863z

    3. [3]

      Q.Z. Zheng, X.M. Zhang, Y. Xu, K. Cheng, Q.C. Jiao, H.L. Zhu. Synthesis, biological evaluation, and molecular docking studies of 2-chloropyridine derivatives possessing 1, 3, 4-oxadiazole moiety as potential antitumor agents[J]. Bioorg. Med. Chem., 2010,18:7836-7841. doi: 10.1016/j.bmc.2010.09.051

    4. [4]

      M. Amir, H. Kumar, S.A. Khan. Synthesis and pharmacological evaluation of pyrazoline derivatives as new anti-inflammatory and analgesic agents[J]. Bioorg. Med. Chem. Lett., 2008,18:918-922. doi: 10.1016/j.bmcl.2007.12.043

    5. [5]

      M.A. Ali, M. Shaharyar, A.A. Siddiqui. Synthesis, structural activity relationship and anti-tubercular activity of novel pyrazoline derivatives[J]. Eur. J. Med. Chem., 2007,42:268-275. doi: 10.1016/j.ejmech.2006.08.004

    6. [6]

      H.J. Park, K. Lee, S.J. Park, B. Ahn, J.C. Lee, H.Y. Cho, K.I. Lee. Identification of antitumor activity of pyrazole oxime ethers[J]. Bioorg. Med. Chem. Lett., 2005,15:3307-3312. doi: 10.1016/j.bmcl.2005.03.082

    7. [7]

      R. Sridhar, P.T. Perumal, S. Etti, G. Shanmugam, M.N. Ponnuswamy, V.R. Prabavathy, N. Mathivanan. Design, synthesis and anti-microbial activity of 1H-pyrazole carboxylates[J]. Bioorg. Med. Chem. Lett., 2004,14:6035-6040. doi: 10.1016/j.bmcl.2004.09.066

    8. [8]

      Z.B. Wu, D.Y. Hu, J.Q. Kuang, H. Cai, S.X. Wu, W. Xue. Synthesis and antifungal activity of N-(substituted pyridinyl)-1-methyl (phenyl)-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide derivatives[J]. Molecules, 2012,17:14205-14218. doi: 10.3390/molecules171214205

    9. [9]

      A. Tanitame, Y. Oyamada, K. Ofuji, M. Fujimoto, N. Iwai, Y. Hiyama, K. Suzuki, H. Ito, H. Terauchi, M. Kawasaki, K. Nagai, M. Wachi, J. Yamagishi. Synthesis and antibacterial activity of a novel series of potent DNA gyrase inhibitors. Pyrazole derivatives[J]. J. Med. Chem., 2004,47:3693-3696. doi: 10.1021/jm030394f

    10. [10]

      X.L. Deng, J. Xie, Y.Q. Li, D.K. Yuan, X.P. Hu, L. Zhang, Q.M. Wang, M. Chi, X.L. Yang. Design, synthesis and biological activity of novel substituted pyrazole amide derivatives targeting EcR/USP receptor[J]. Chin. Chem. Lett., 2016,27:566-570. doi: 10.1016/j.cclet.2016.02.009

    11. [11]

      N. Nayak, J. Ramprasad, U. Dalimba, P. Yogeeswari, D. Sriram. Synthesis and antimycobacterial screening of new N-(4-(5-aryl-3-(5-methyl-1, 3, 4-oxadiazol-2-yl)-1H-pyrazol-1-yl) phenyl)-4-amide derivatives[J]. Chin. Chem. Lett., 2016,27:365-369. doi: 10.1016/j.cclet.2016.01.015

    12. [12]

      N.D. Vala, H.H. Jardosh, M.P. Patel. PS-TBD triggered general protocol for the synthesis of 4H-chromene, pyrano[4, 3-b]pyran and pyrano[3, 2-c]chromene derivatives of 1H-pyrazole and their biological activities[J]. Chin. Chem. Lett., 2016,27:168-172. doi: 10.1016/j.cclet.2015.09.020

    13. [13]

      S.L. Wang, Y.J. Shi, H.B. He, Y. Li, Y. Li, H. Dai. Synthesis and bioactivity of novel pyrazole oxime derivatives containing oxazole ring[J]. Chin. Chem. Lett., 2015,26:672-674. doi: 10.1016/j.cclet.2015.04.017

    14. [14]

      R. Zeun, G. Scalliet, M. Oostendorp. Biological activity of sedaxane a novel broad-spectrum fungicide for seed treatment[J]. Pest Manag. Sci., 2013,69:527-534. doi: 10.1002/ps.3405

    15. [15]

      L.H. Hand, H.J. Moreland. Surface water mineralization of isopyrazam according to OECD 309:observations on implementation of the new data requirement within agrochemical regulation[J]. Environ. Toxicol. Chem., 2014,33:516-524. doi: 10.1002/etc.v33.3

    16. [16]

      A. Gulkowska, I.J. Buerge, T. Poiger. Online solid phase extraction LC-MS/MS method for the analysis of succinate dehydrogenase inhibitor fungicides and its applicability to surface water samples[J]. Anal. Bioanal. Chem., 2014,406:6419-6427. doi: 10.1007/s00216-014-8073-4

    17. [17]

      S.S. Li, X.G. Liu, C. Chen, F.S. Dong, J. Xu, Y.Q. Zheng. Degradation of fluxapyroxad in soils and water/sediment systems under aerobic or anaerobic conditions[J]. Bull. Environ. Contam. Toxicol., 2015,95:45-50. doi: 10.1007/s00128-015-1556-y

    18. [18]

      G.V.S. Kumar, Y.R. Prasad, S.M. Chandrashekar. Synthesis and pharmacological evaluation of some novel 4-isopropyl thiazole-based sulfonyl derivatives as potent antimicrobial and antitubercular agents[J]. Med. Chem. Res., 2013,22:4239-4252. doi: 10.1007/s00044-012-0431-1

    19. [19]

      M.A. Bhat. Synthesis and anti-mycobacterial activity of new 4-thiazolidinone and 1, 3, 4-oxadiazole derivatives of isoniazid[J]. Acta Pol. Pharm., 2014,71:763-770.  

    20. [20]

      D. Pal, R. Tripathi, D.D. Pandey, P. Mishra. Synthesis, characterization, antimicrobial, and pharmacological evaluation of some 2, 5-disubstituted sulfonyl amino 1, 3, 4-oxadiazole and 2-amino-disubstituted 1, 3, 4-thiadiazole derivatives[J]. J. Adv. Pharm. Technol. Res., 2014,5:196-201. doi: 10.4103/2231-4040.143040

    21. [21]

      M.M. Gamal El-Din, M.I. El-Gamal, M.S. Abdel-Maksoud, K.H. Yoo, C.H. Oh. Synthesis and in vitro antiproliferative activity of new 1, 3, 4-oxadiazole derivatives possessing sulfonamide moiety[J]. Eur. J. Med. Chem., 2015,90:45-52. doi: 10.1016/j.ejmech.2014.11.011

    22. [22]

      P. Li, L. Shi, X. Yang, L. Yang, X. Chen, F. Wu, Q. Shi, W.M. Xu, M. He, D.Y. Hu, B.A. Song. Design, synthesis, and antibacterial activity against rice bacterial leaf blight and leaf streak of 2, 5-substituted-1, 3, 4-oxadiazole/thiadiazole sulfone derivative[J]. Bioorg. Med. Chem. Lett., 2014,24:1677-1680. doi: 10.1016/j.bmcl.2014.02.060

    23. [23]

      P. Li, L. Shi, M. Gao, X. Yang, W. Xue, L.H. Jin, D.Y. Hu, B.A. Song. Antibacterial activities against rice bacterial leaf blight and tomato bacterial wilt of 2-mercapto-5-substituted-1, 3, 4-oxadiazole/thiadiazole derivatives[J]. Bioorg. Med. Chem. Lett., 2015,25:481-484. doi: 10.1016/j.bmcl.2014.12.038

    24. [24]

      W.M. Xu, S.Z. Li, M. He, S. Yang, X.Y. Li, P. Li. Synthesis and bioactivities of novel thioether/sulfone derivatives containing 1, 2, 3-thiadiazole and 1, 3, 4-oxadiazole/thiadiazole moiety[J]. Bioorg. Med. Chem. Lett., 2013,23:5821-5824. doi: 10.1016/j.bmcl.2013.08.107

    25. [25]

      P.Y. Wang, L. Zhou, J. Zhou, Z.B. Wu, W. Xue, B.A. Song, S. Yang. Synthesis and antibacterial activity of pyridinium-tailored 2, 5-substituted-1, 3, 4-oxadiazole thioether/sulfoxide/sulfone derivatives[J]. Bioorg. Med. Chem. Lett., 2016,26:1214-1217. doi: 10.1016/j.bmcl.2016.01.029

    26. [26]

      P.Y. Wang, M.N. Gao, L. Zhou, Z.B. Wu, D.Y. Hu, J. Hu, S. Yang. Synthesis and antibacterial activity of pyridinium-tailored aromatic amphiphiles[J]. Bioorg. Med. Chem. Lett., 2016,26:1136-1139. doi: 10.1016/j.bmcl.2016.01.053

    27. [27]

      X. Wang, J. Yin, L. Shi, G. Zhang, B.A. Song. Design, synthesis, and antibacterial activity of novel Schiff base derivatives of quinazolin-4(3H)-one[J]. Eur. J. Med. Chem., 2014,77:65-74. doi: 10.1016/j.ejmech.2014.02.053

    28. [28]

      T.K. Chattapadhyay, P. Dureja. Antifungal activity of 4-methyl-6-alkyl-2Hpyran-2-ones[J]. J. Agric. Food Chem., 2006,54:2129-2133. doi: 10.1021/jf052792s

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