Home Chemistry Heterocyclic Building Blocks Pyrimidines 4,6-Dichloropyrimidin-2-Amine
Nucleophilic Aromatic Substitution (SNAr): The amino group can act as a nucleophile in substitution reactions, leading to the displacement of one of the chlorines on the pyrimidine ring.
Reaction with Acyl Chlorides or Acid anhydrides: The amino group can react with acyl chlorides or acid anhydrides to form amide derivatives.
Reaction with Alkyl Halides: The amino group can undergo alkylation reactions with alkyl halides to form alkylated amine derivatives.
Reaction with Carbonyl Compounds: The amino group can participate in reductive amination reactions with carbonyl compounds, such as aldehydes or ketones, to form secondary amines.
Substitution Reactions at Chlorine Positions: The chlorine atoms on the pyrimidine ring can undergo substitution reactions under certain conditions.
Intramolecular Cyclization: The amino group and chlorines on the pyrimidine ring may participate in intramolecular cyclization reactions under specific conditions, leading to the formation of cyclic compounds.
Oxidation of Amino Group: The amino group can potentially undergo oxidation reactions to form corresponding nitro or other oxidized derivatives.
Reaction with Formic Acid or Formyl Chloride: The amino group can react with formic acid or formyl chloride to form N-formyl derivatives.
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N-(2-Amino-4,6-dichloropyrimidine-5-yl)formamide
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2-Amino-4,6-dichloropyrimidine-5-carboxaldehyde
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2-Amino-4,6-dichloropyrimidine-5-carbonitrile
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