Abstract
It was established that hard bases replace the methylsulfonyl groups and that soft bases replace the chlorine atoms in 2,4,6-tris(methylsulfonyl)-3,5-dichloropyridine.
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S. D. Moshchitskii, G. A. Zalesskii, E. A. Romanenko, and V. P. Kukhar', Khim. Geterotsikl. Soedin., No. 3, 369 (1976).
R. G. Pearson, Usp. Khim., 40, 1259 (1971).
S. D. Moshchitskii, G. A. Zalesskii, and L. M. Yagupol'skii, Khim. Geterotsikl. Soedin., No. 6, 802 (1975).
R. G. Pearson and J. Songstad, J. Am. Chem. Soc., 89, 1827 (1967).
H. I. Hertog and I. P. Wibaut, Rec. Trav. Chim., 55, 122 (1936).
J. Bernstein, B. Stearns, M. Dexter, and W. A. Lott, J. Am. Chem. Soc., 69, 1147 (1974).
A. Roedig, K. Grohe, and D. Klatt, Ber., 99, 2818 (1966).
Belgian Patent No. 740278 (1973); Ref. Zh. Khim., 2N164P (1974).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii. No. 7, pp. 915–919, July, 1976.
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Moshchitskii, S.D., Zalesskii, G.A. & Kukhar', V.P. Nucleophilic substitution reactions of 2,4,6-tris(methylsulfonyl)-3.5-dichloropyridine. Chem Heterocycl Compd 12, 760–763 (1976). https://doi.org/10.1007/BF00477007
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DOI: https://doi.org/10.1007/BF00477007