Home Chemistry Heterocyclic Building Blocks Pyrimidines 2-Methoxypyrimidine
Nucleophilic Substitution: The methoxy group can act as a nucleophile in substitution reactions. For instance, it can be replaced by a nucleophile in the presence of an appropriate electrophile.
Acylation and Alkylation: The nitrogen atoms in the pyrimidine ring can undergo acylation or alkylation reactions. This involves the introduction of acyl or alkyl groups to the nitrogen atoms.
Oxidation: The compound may undergo oxidation reactions under certain conditions, potentially leading to the formation of oxidation products.
Nucleophilic Aromatic Substitution (SNAr): The pyrimidine ring can participate in nucleophilic aromatic substitution reactions where the methoxy group or other substituents may be replaced by nucleophiles.
Reductive Reactions: The compound may undergo reduction reactions, depending on the reaction conditions and the choice of reducing agents.
N-Heterocyclic Carbene (NHC) Formation: The nitrogen atoms in the pyrimidine ring can form N-heterocyclic carbenes under certain reaction conditions.
Metalation: The pyrimidine ring may undergo metalation reactions, where a metal atom is introduced at a specific position in the molecule.
Condensation Reactions: 2-Methoxypyrimidine may participate in condensation reactions with other reactive compounds, forming new bonds and yielding more complex structures.
Catalytic Reactions: The compound may be involved in various catalytic reactions, depending on the presence of suitable catalysts.
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5-Bromo-2-methoxy-4-(trifluoromethyl)pyrimidine
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