Home Chemistry Heterocyclic Building Blocks Pyrimidines 4-Methoxypyrimidin-2-Amine
Nucleophilic Substitution Reactions: The amino group can act as a nucleophile and undergo substitution reactions with electrophiles. For instance, it might react with alkyl halides or acyl halides to form substituted products.
Acylation Reactions: The amino group can react with acyl chlorides or acid anhydrides to form amides. This type of reaction is known as acylation.
Alkylation Reactions: The amino group may also undergo alkylation reactions with alkyl halides, leading to the formation of alkyl-substituted amines.
Condensation Reactions: The amino group can participate in condensation reactions with carbonyl compounds (aldehydes or ketones) to form imines or Schiff bases.
Nucleophilic Aromatic Substitution (SNAr): The pyrimidine ring can undergo nucleophilic aromatic substitution reactions under certain conditions, especially if there are activating or directing groups on the ring.
Reduction Reactions: The nitrogen in the amino group can be reduced to form a variety of products, depending on the choice of reducing agent. For example, it might be reduced to form amines.
Dehydration Reactions: The compound might undergo dehydration reactions under appropriate conditions, leading to the elimination of water and the formation of double bonds.
Oxidation Reactions: The methoxy group or the amino group might be susceptible to oxidation under certain conditions, leading to the formation of corresponding oxidized products.
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