Abstract
Treatment of 2-chloro-6-thio-7-methylpurine with aniline, piperidine, or morpholine with heating in DMF gives 2-phenylamino(piperidino or morpholino)-6-thio-7-methylpurine. The scheme for the formation of the side products 2,6-dithio-and 2,6-dipiperidino-7-methylpurine is discussed.
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References
M. D.Mashkovskii,Medicinals [in Russian], Torsing, Khar'kov (1997), Vol. 2, 454.
P. B. Petrov and V. M. Man'ko,Immunodepressors [in Russian], Meditsina, Moscow (1971), pp. 107, 127, 183.
L. A. Gutorov, USSR Inventor's Certificate 207918,Byul. Izobret., No. 3 (1968).
E. Fischer,Chem. Ber.,31, 431 (1898).
J. Roch, GB Patent 864145,Chem. Abstr.,55, 18782 (1961).
G. Elion,J. Org. Chem.,27, 2478 (1962).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 82–84, January, 2000.
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Kochergin, P.M., Aleksandrova, E.V. & Korsunskii, V.S. Products of the reaction of 2-chloro-6-thio-7-methyl-purine with amines. Chem Heterocycl Compd 36, 74–76 (2000). https://doi.org/10.1007/BF02256849
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DOI: https://doi.org/10.1007/BF02256849