Abstract
The reaction between 5-amino-4-imino-1(2)-substituted-1(2)
H-4,5-dihydropyrazolo[3,4-
d]pyrimidines and several commercially available reactants afforded new heterocycles with a conserved pyrazolo[3,4-
d]pyrimidine nucleus. The key intermediates employed proved to be suitable compounds by virtue of their two vicinal amino and imino groups that were used to obtain five, six and seven-membered rings.
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