Home Chemistry Heterocyclic Building Blocks Pyrimidines N-Benzyl-9H-Purin-6-Amine
Nucleophilic Substitution: The amino group can act as a nucleophile and undergo substitution reactions with electrophiles. For example, it can react with alkyl halides to form N-alkylated products.
Dehydration: Under certain conditions, N-benzyl-9H-purin-6-amine can undergo dehydration reactions to form imines or enamines, depending on the reaction conditions and the presence of other functional groups.
Oxidation: The purine ring system can be subject to oxidation reactions, leading to the formation of various products. For instance, it may be oxidized to form N-oxide derivatives or further oxidized to produce other functional groups.
Reduction: Depending on the reaction conditions and reagents used, the molecule can undergo reduction reactions. For example, the imine or carbonyl group formed through acylation or oxidation reactions can be reduced to form a amide.
Metal-Catalyzed Reactions: Transition metal-catalyzed reactions, such as cross-coupling reactions or C-H activation reactions, can be employed to modify the benzyl substituent or the purine ring itself.
Nucleophilic Aromatic Substitution: The benzyl group can undergo nucleophilic aromatic substitution reactions, where the benzene ring is substituted with various nucleophiles under appropriate reaction conditions.
Ring Closure: Depending on the reaction conditions and functional groups present, N-benzyl-9H-purin-6-amine may participate in ring-closure reactions to form cyclic compounds.
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2-(((9H-Purin-6-yl)amino)methyl)phenol
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