Home Chemistry Heterocyclic Building Blocks Imidazoles Imidazo[1,2-C]Pyrimidine
Nucleophilic Substitution: Imidazo[1,2-c]pyrimidine can undergo nucleophilic substitution reactions at various positions on the ring system. For example, nucleophiles can attack the electrophilic carbon atoms in the imidazole and pyrimidine rings.
Electrophilic Substitution: Imidazo[1,2-c]pyrimidine can also undergo electrophilic aromatic substitution reactions. This can involve the addition of electrophilic reagents to the aromatic rings, leading to the substitution of hydrogen atoms with various functional groups.
Oxidation and Reduction Reactions: The nitrogen atoms in the imidazole and pyrimidine rings can undergo oxidation or reduction reactions to yield different compounds with altered properties.
Alkylation and Acylation: Imidazo[1,2-c]pyrimidine can react with alkyl or acyl halides in the presence of a base to introduce alkyl or acyl groups onto the nitrogen atoms.
Cyclization Reactions: Depending on the reaction conditions and reagents, imidazo[1,2-c]pyrimidine can participate in various cyclization reactions, leading to the formation of fused ring systems or other heterocyclic compounds.
Cross-Coupling Reactions: Imidazo[1,2-c]pyrimidine can be used in cross-coupling reactions, where it serves as a partner in the formation of new carbon-carbon or carbon-heteroatom bonds.
Ring Opening Reactions: Under certain conditions, imidazo[1,2-c]pyrimidine can undergo ring-opening reactions, leading to the cleavage of the fused ring system and the formation of open-chain compounds.
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8-Chloro-5,7-dimethylimidazo[1,2-c]pyrimidine
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5-Chloro-8-iodoimidazo[1,2-c]pyrimidine
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