Home Chemistry Heterocyclic Building Blocks Pyrimidines 2,4,6-Triphenylpyrimidine
Arylation: The phenyl groups in 2,4,6-triphenylpyrimidine can undergo arylation reactions, where they can be further functionalized with various aryl groups. For example, you can perform a Suzuki coupling reaction to introduce different aryl groups to the molecule.
Halogenation: The phenyl rings can be halogenated (e.g., bromination or chlorination) to introduce halogen atoms to the molecule. This can be useful for further reactions or modifications.
Nucleophilic Substitution: If there are suitable leaving groups on the phenyl rings, nucleophilic substitution reactions can occur. For example, you can replace a leaving group with a nucleophile under appropriate conditions.
Amination: You can introduce amino groups into the molecule by performing amination reactions, such as nucleophilic aromatic substitution (SNAr) or reductive amination.
Cross-Coupling Reactions: Cross-coupling reactions like the Heck, Sonogashira, or Buchwald-Hartwig reactions can be used to attach various functional groups to the phenyl rings.
Cycloaddition Reactions: Depending on the specific structure and conditions, 2,4,6-triphenylpyrimidine may undergo various cycloaddition reactions, such as Diels-Alder reactions or [2+2] cycloadditions, if appropriate reagents and conditions are applied.
Substitution Reactions: If there are substituents on the phenyl rings, they may undergo substitution reactions, such as nucleophilic aromatic substitution, to replace one group with another.
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4-(3,5-Dibromophenyl)-2,6-diphenylpyrimidine
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