Home Chemistry Heterocyclic Building Blocks Pyrimidines N-Phenyl-4-(Pyridin-3-Yl)Pyrimidin-2-Amine
Arylation reactions: The N-phenyl group can undergo various reactions, such as electrophilic aromatic substitution or transition metal-catalyzed cross-coupling reactions (e.g., Suzuki-Miyaura coupling or Buchwald-Hartwig amination). These reactions can introduce different aryl groups at the N-phenyl position.
Pyrimidine ring modifications: The pyrimidine ring can undergo various transformations, such as N-alkylation, N-oxidation, or halogenation, to introduce different substituents or functional groups on the pyrimidine ring.
Pyridine ring modifications: The pyridine ring can also be modified through various reactions, including electrophilic aromatic substitution, nucleophilic substitution, or metal-catalyzed reactions. These reactions can lead to the introduction of different substituents on the pyridine ring.
Condensation reactions: The amine group can participate in condensation reactions with carbonyl compounds to form imines or imine derivatives. This can be useful for synthesizing various heterocyclic compounds.
Reduction reactions: The imine functionality formed in condensation reactions can be reduced to an amine using reducing agents like sodium borohydride or lithium aluminum hydride.
Cyclization reactions: Depending on the reaction conditions and reagents used, the molecule may undergo cyclization reactions to form fused ring systems or other heterocyclic compounds.
Functional group transformations: Various functional group transformations, such as oxidation, reduction, acylation, and esterification, can be applied to modify different parts of the molecule.
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Methyl 4-methyl-3-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)benzoate
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4-Methyl-3-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)benzoic acid
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N-(2-Methyl-5-nitrophenyl)-4-(pyridin-3-yl)pyrimidin-2-amine
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Ethyl 4-methyl-3-((4-(pyridin-3-yl)pyrimidin-2-yl)amino)benzoate
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