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Acetoacetanilides in synthesis of 4-aryl-5-arylcarbamoyl-6-methyl-3-cyanopyridine-2(1H)-thiones

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The reaction of acetoacetanilides with arylmethylenecyanothioacetamides leads to 4-aryl-5-arylcarbamoyl-6-methyl-3-cyanopyridine-2(1H)-thiones, based on which we have obtained substituted 2-alkylthiopyridines and thieno[2,3-b]pyridines.

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References

  1. V. P. Litvinov, L. A. Rodinovskaya, Yu. A. Sharanin, A. M. Shestopalov, and A. Senning, Sulfur Reports,13, 1 (1992).

    CAS  Google Scholar 

  2. A. A. Krauze, A. G. Odynets, A. A. Verreva, S. K. Germane, A. N. Kozhukov, and G. Ya. Dubur, Khim.-farm. Zh.,25, 40 (1991).

    CAS  Google Scholar 

  3. V. V. Kastron, R. O. Vitolinya, and G. Ya. Dubur, Khim.-farm. Zh., No. 6, 14 (1990).

    Google Scholar 

  4. F. S. Babichev, Yu. A. Sharanin, V. P. Litvinov, V. K. Promonenkov, and Yu. M. Volovenko, Intramolecular Reaction of Nitrile with C−H, O−H, and S−H Groups [in Russian], Naukova Dumka (1985).

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T. G. Shevchenko Lugansk State Pedagogical Institute, Lugansk 348011. N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Moscow 117913. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 560–568, April, 1997.

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Dyachenko, V.D., Krivokolysko, S.G. & Litvinov, V.P. Acetoacetanilides in synthesis of 4-aryl-5-arylcarbamoyl-6-methyl-3-cyanopyridine-2(1H)-thiones. Chem Heterocycl Compd 33, 481–488 (1997). https://doi.org/10.1007/BF02321397

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  • DOI: https://doi.org/10.1007/BF02321397

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