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Direct oxidative SNH amidation of 1,3,7-triazapyrene

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Chemistry of Heterocyclic Compounds Aims and scope

6-Acylamino-1,3,7-triazapyrenes have been synthesized for the first time by direct oxidative nucleophilic substitution of hydrogen.

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Scheme 1
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Notes

  1. 13C NMR spectrum of compound 2d could not be recorded due to insufficient solubility.

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The work was performed with financial support from the Ministry of Education and Science of the Russian Federation (project No. 4.141.2014/K).

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Authors and Affiliations

  1. North Caucasus Federal University, 1a Pushkin St., Stavropol’, 355009, Russia

    Ivan V. Borovlev, Oleg P. Demidov, Nadezhda A. Kurnosova, Gulminat A. Amangasieva & Elena K. Avakyan

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  1. Ivan V. Borovlev
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  2. Oleg P. Demidov
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  3. Nadezhda A. Kurnosova
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  4. Gulminat A. Amangasieva
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Correspondence to Ivan V. Borovlev.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, 2015, 51(2), 170–175

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Borovlev, I.V., Demidov, O.P., Kurnosova, N.A. et al. Direct oxidative SNH amidation of 1,3,7-triazapyrene. Chem Heterocycl Comp 51, 170–175 (2015). https://doi.org/10.1007/s10593-015-1677-6

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