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Reaction of 2-mercaptopyrimidines with some α,ω-dihaloalkanes

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

In the reaction of some 2-mercapto-4,6-disubstituted pyrimidines with differentα,ω-dihaloalkanes, thiazolepyrimidine and pyrimidothiazine salts, 2-(ω-haloalkylthio)-4,6-disubstituted pyrimidines, andα,ω-bis (4,6-disubstituted pyrimidinyl-2-thio) alkanes are formed. The structure of the products of the reactions is a function of the nature of the substituents in the pyrimidine ring, the number of methylene groups in theα,ω-dihaloalkanes, and the ratio of the reagents.

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Authors and Affiliations

  1. A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Branch, Academy of Sciences of the USSR, USSR

    A. S. Mikhailov, N. G. Pashkurov, V. S. Reznik & G. I. Podzigun

Authors
  1. A. S. Mikhailov
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  2. N. G. Pashkurov
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  3. V. S. Reznik
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  4. G. I. Podzigun
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp. 1396–1402, June, 1984.

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Mikhailov, A.S., Pashkurov, N.G., Reznik, V.S. et al. Reaction of 2-mercaptopyrimidines with some α,ω-dihaloalkanes. Russ Chem Bull 33, 1285–1291 (1984). https://doi.org/10.1007/BF00949003

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  • DOI: https://doi.org/10.1007/BF00949003

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