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Synthesis of Alkyl 5,6-Dialkyl-2-amino-3-cyanopyridine-4-carboxylates

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

An unusual route has been found for the hydrolysis of 3-amino-1,1-dialkoxy-6,7-dialkyl-4-aryl-3a,4,5,7a-tetrahydro-1H-pyrrolo[3,4-c]pyridine-3a,7a-dicarbonitriles in acidic medium which leads to the formation of alkyl 5,6-dialkyl-2-amino-3-cyanopyridine-4-carboxylates.

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Authors and Affiliations

  1. I. N. Ul'yanov Chuvash State University, Cheboksary, 428015, Russia

    A. N. Vasiliev, Ya. S. Kayukov, O. E. Nasakin, A. N. Lyshchikov, V. N. Nesterov, O. V. Kayukova & O. V. Poulkherovskaya

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  1. A. N. Vasiliev
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  2. Ya. S. Kayukov
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  3. O. E. Nasakin
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  4. A. N. Lyshchikov
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  5. V. N. Nesterov
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  6. O. V. Kayukova
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  7. O. V. Poulkherovskaya
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Vasiliev, A.N., Kayukov, Y.S., Nasakin, O.E. et al. Synthesis of Alkyl 5,6-Dialkyl-2-amino-3-cyanopyridine-4-carboxylates. Chemistry of Heterocyclic Compounds 37, 309–314 (2001). https://doi.org/10.1023/A:1017503015471

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  • DOI: https://doi.org/10.1023/A:1017503015471

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