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Microwave-assisted synthesis of 3-substituted-6-ferrocene methylene-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles

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Abstract

A series of triazolo-thiadiazole derivatives containing ferrocene were synthesized under microwave assistance. Compared with the phosphorus oxychloride method, the microwave method has the advantages of simple operation, short reaction time, fast reaction rate and high yield. The effects of different reaction conditions were explored, and under the optimized conditions, the products were obtained in good yields (up to 80%).

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References

  1. Badr SM, Barwa RM (2011) Bioorg Med Chem 19:4506–4512

    Article  CAS  PubMed  Google Scholar 

  2. Mathew V, Keshavayya J, Vaidya VP (2006) Eur J Med Chem 41:1048–1058

    Article  CAS  PubMed  Google Scholar 

  3. Sun XH, Tao Y, Liu YF (2008) Chin J Org Chem 28:155–159

    CAS  Google Scholar 

  4. Bagihalli GB, Avaji PGS, Patil A (2008) Eur J Med Chem 43:2639–2649

    Article  CAS  PubMed  Google Scholar 

  5. Bayrak H, Demirbas A, Karaoglu SA (2009) Eur J Med Chem 44:1057–1066

    Article  CAS  PubMed  Google Scholar 

  6. Deng XQ, Song MX, Zheng Y (2014) Eur J Med Chem 73:217–224

    Article  CAS  PubMed  Google Scholar 

  7. Sujith KV, Kalluraya B, Adhikari A (2011) Chin Chem Lett 22:508–510

    Article  CAS  Google Scholar 

  8. Amir M, Kumar H, Javed SA (2007) Bioorg Med Chem Lett 17:4504–4508

    Article  CAS  PubMed  Google Scholar 

  9. Li YJ, Liu LJ, Jin K (2010) Chin Chem Lett 21:293–296

    Article  CAS  Google Scholar 

  10. Aggarwal N, Kumar R, Dureja P (2011) Eur J Med Chem 46:4089–4099

    Article  CAS  PubMed  Google Scholar 

  11. Li YS, Li DJ (2009) Chem Res Appl 21:1038–1041

    CAS  Google Scholar 

  12. Tan P, Yu AH, Yan J, Mi YS (2011) Chem J Chin Univ 32:1083–1087

    CAS  Google Scholar 

  13. Patel RV, Park SW (2014) Eur J Med Chem 71:24–30

    Article  CAS  PubMed  Google Scholar 

  14. Zhang F, Wen Q, Wang SF (2014) Bioorg Med Chem Lett 24:90–95

    Article  CAS  PubMed  Google Scholar 

  15. Zhu YP, Olson SH, Vosatka AH (2008) Bioorg Med Chem Lett 18:3405–3411

    Article  CAS  PubMed  Google Scholar 

  16. Kumar GVS, Rajendraprasad Y, Mallikarjuna BP (2010) Eur J Med Chem 45:2063–2074

    Article  CAS  Google Scholar 

  17. Sahi S, Bhardwaj M, Paul S (2014) Tetrahedron Lett 55:3809–3812

    Article  CAS  Google Scholar 

  18. Gilani SJ, Khan SA, Siddiqui N (2010) Bioorg Med Chem Lett 20:4762–4765

    Article  CAS  PubMed  Google Scholar 

  19. Swamy SN, Basappa, Priya BS (2006) Eur J Med Chem 41:531–538

    Article  CAS  PubMed  Google Scholar 

  20. Saeed A, Channar PA, Iqbal Q (2016) Chin Chem Lett 27:37–40

    Article  CAS  Google Scholar 

  21. Akhter MW, Hassan MZ, Amir M (2014) Arab J Chem 7:955–963

    Article  CAS  Google Scholar 

  22. Ibrahim DA (2009) Eur J Med Chem 40:2776–2781

    Article  CAS  Google Scholar 

Download references

Acknowledgements

We are grateful for the financial support from 973 preliminary Projects (2014CB260411) and the Key Laboratory project of Shaanxi Provincial Department of Education (13J017).

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Correspondence to Hong Xin.

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Liu, Y., Xin, H., Yin, J. et al. Microwave-assisted synthesis of 3-substituted-6-ferrocene methylene-1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles. Transit Met Chem 43, 381–385 (2018). https://doi.org/10.1007/s11243-018-0219-3

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  • DOI: https://doi.org/10.1007/s11243-018-0219-3

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