The synthesis of 6-substituted purine derivatives involves chemically modifying the purine structure to introduce various substituents at the 6-position. This modification can be achieved through organic synthesis methods, such as nucleophilic substitution, ring closure reactions, and other chemical transformations. The choice of substituent at the 6-position can significantly impact the pharmacological properties of the resulting compounds.
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1-(1-chloro-2-hydroxy-3-propanyl)-4-[bis(4-fluorophenyl)-methyl]-piperazine
