Abstract
Condensation of 4-amino-5-nitro-6-chloropyrimidine with 2-amino-1,3-dihydroxypropane and 2-amino-1,4-dihydroxybutane gave 4-amino-5-nltro-6-dihydroxyalkylpyrimidines, which are cyclized to 2-(9-adeninyl)alkanediols after reduction of the nitro group.
Similar content being viewed by others
Literature cited
M. Yu. Lidak, Ya. Ya. Shluke, B. V. Zarinya, and S. E. Poritere, Khim. Geterotsikl. Soedin., 2, 262 (1971).
T. Suami, Y. Sato, Y. Fukai, and Y. Sakota, J. Heterocycl. Chem., 6, 663 (1969).
W. R. Boon, W. G. M. Jones, and G. R. Ramage, J. Chem. Soc., 99 (1951).
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 129–130, January, 1973.
Rights and permissions
About this article
Cite this article
Lidak, M.Y., Zarinya, B.V. & Shluke, Y.Y. New method for the synthesis of 2-(9-adeninyl)alkanediols. Chem Heterocycl Compd 9, 117–119 (1973). https://doi.org/10.1007/BF00476167
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00476167