Home Chemistry Heterocyclic Building Blocks Pyrimidines 2-Phenoxypyrimidine
Arylation: 2-Phenoxypyrimidine can undergo various arylation reactions, where an aryl group (such as phenyl, benzyl, or other aromatic groups) is added to the pyrimidine ring. This can be achieved through metal-catalyzed reactions like Suzuki-Miyaura coupling or Buchwald-Hartwig amination.
Halogenation: The phenyl ring can be halogenated using halogenating reagents such as bromine or chlorine in the presence of a Lewis acid catalyst. This would result in the substitution of hydrogen atoms on the phenyl ring with halogen atoms.
Nucleophilic Substitution: 2-Phenoxypyrimidine contains a nucleophilic nitrogen atom in the pyrimidine ring. It can undergo nucleophilic substitution reactions with electrophiles. For example, it can react with alkyl halides to form N-alkylated products under appropriate conditions.
Reductive Amination: The nitrogen atom in the pyrimidine ring can also participate in reductive amination reactions, where it can react with aldehydes or ketones in the presence of reducing agents like sodium borohydride to form N-substituted derivatives.
Ring Cleavage: Depending on the reaction conditions and reagents used, 2-phenoxypyrimidine may undergo ring-opening reactions or cleavage of the pyrimidine ring to form different products.
Oxidation and Reduction: The phenyl group can undergo oxidation or reduction reactions depending on the choice of reagents and reaction conditions. For example, it can be oxidized to a phenolic compound or reduced to a cyclohexyl group.
Condensation Reactions: 2-Phenoxypyrimidine can participate in various condensation reactions with appropriate reagents to form heterocyclic compounds or other derivatives.
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Methyl 4-((5-bromopyrimidin-2-yl)oxy)benzoate
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Methyl 2-((4,6-dimethylpyrimidin-2-yl)oxy)benzoate
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Methyl 2-(5-bromopyrimidin-2-yloxy)benzoate
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2-((4,6-Dimethoxypyrimidin-2-yl)oxy)benzoic acid
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