Home Chemistry Heterocyclic Building Blocks Pyrimidines Methyl Pyrimidine-2-Carboxylate
Hydrolysis: The ester group in methyl pyrimidine-2-carboxylate can undergo hydrolysis under acidic or basic conditions, leading to the formation of pyrimidine-2-carboxylic acid and methanol.
Nucleophilic Substitution: The pyrimidine ring, particularly the carbon atoms adjacent to the carboxylate group, can undergo nucleophilic substitution reactions. This can involve displacement of the leaving group (usually the methoxy group) by a nucleophile.
Amidation: The carboxylate group can undergo amidation reactions, reacting with amines or ammonia to form amide derivatives.
Esterification: The carboxylic acid group resulting from hydrolysis can undergo esterification reactions with alcohols, regenerating theester
Reduction: The carbonyl group in the ester can be reduced to the corresponding alcohol under appropriate conditions.
Cyclization: The compound may undergo intramolecular cyclization reactions under certain conditions, especially if there are functional groups that can participate in such reactions.
Oxidation: The compound can potentially undergo oxidation reactions, depending on the reaction conditions and the presence of suitable oxidizing agents.
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