Home Chemistry Heterocyclic Building Blocks Pyrimidines N-Phenylpyrimidin-4-Amine
Arylation: N-phenylpyrimidin-4-amine contains a phenyl group, which is an aromatic ring. It can undergo various arylation reactions, such as Suzuki-Miyaura coupling, Buchwald-Hartwig amination, or Stille coupling, to introduce different aryl groups at the nitrogen atom.
Alkylation: The amine group can be alkylated using alkyl halides to form N-alkylated derivatives.
Substitution reactions: The amino group on the pyrimidine ring can undergo nucleophilic substitution reactions with electrophiles, leading to the formation of various substituted pyrimidines.
Condensation reactions: N-phenylpyrimidin-4-amine can participate in condensation reactions with carbonyl compounds, such as ketones or aldehydes, to form pyrimidine derivatives.
Heterocyclization: It can undergo heterocyclization reactions with appropriate reagents to form fused ring systems or other heterocyclic compounds.
Halogenation: It can undergo halogenation reactions, such as bromination or chlorination, at various positions on the molecule.
Cyclization: Depending on the reaction conditions, N-phenylpyrimidin-4-amine can participate in cyclization reactions to form different cyclic compounds.
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(2-((2,5-Dichloropyrimidin-4-yl)amino)phenyl)methanol
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N-(tert-Butyl)-3-((2-chloro-5-methylpyrimidin-4-yl)amino)benzenesulfonamide
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2,5-Dichloro-N-(2-(isopropylthio)phenyl)pyrimidin-4-amine
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5-Bromo-2-chloro-N-(2-fluoro-5-nitrophenyl)pyrimidin-4-amine
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(2-((2,5-Dichloropyrimidin-4-yl)amino)phenyl)dimethylphosphine oxide
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6-Chloro-N-(3,4-dichlorophenyl)pyrimidin-4-amine
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