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An efficient access to 2,3-diarylimidazo[1,2-a]pyridines via silver(I)-catalyzed C-H bond functionalization

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Abstract

An efficient and economic Ag-catalyzed method for the direct cross-coupling of unactivated imidazo[1,2-a]pyridines with arylboronic acids has been developed. This approach leads to the formation of corresponding 2,3-diarylimidazo[1,2-a]pyridine derivatives as biological and pharmaceutical materials of interest in good yields under mild reaction conditions.

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Acknowledgements

This research was supported by the Iran National Science Foundation (INSF).

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Authors and Affiliations

  1. Medicinal and Natural Products Chemistry Research Center, Shiraz University of Medical Sciences, Shiraz, Iran

    Mehdi Khoshneviszadeh

  2. School of Chemistry, College of Science, University of Tehran, PO Box 14155-6455, Tehran, Iran

    Mehdi Soheilizad & Maryam Fardpour

  3. Tehran University of Medical Science, Endocrinology and Metabolism Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran, Iran

    Mohammad Mahdavi

Authors
  1. Mehdi Khoshneviszadeh
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  2. Mehdi Soheilizad
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  3. Maryam Fardpour
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  4. Mohammad Mahdavi
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Corresponding author

Correspondence to Mohammad Mahdavi.

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Khoshneviszadeh, M., Soheilizad, M., Fardpour, M. et al. An efficient access to 2,3-diarylimidazo[1,2-a]pyridines via silver(I)-catalyzed C-H bond functionalization. Monatsh Chem 148, 1817–1821 (2017). https://doi.org/10.1007/s00706-017-1950-8

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  • DOI: https://doi.org/10.1007/s00706-017-1950-8

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