In this paper the solid phase synthesis of various substituted purines is d
escribed starting from 4,6-dichloro-5-nitropyrimidine, The 4,6-dichloro-5-n
itropyrimidine was coupled to Rink amide resin followed by displacement of
the second chloride by an amino compound. Reduction of the nitro compound p
roved to be problematic but was achieved using lithium aluminum hydride/alu
minum trichloride. The diamines (13) were then elaborated to purines by thr
ee different routes.