Home Chemistry Heterocyclic Building Blocks Pyrimidines 2-Methylpyrimidin-4-Ol
Acetylation: The hydroxyl group in 2-methylpyrimidin-4-ol can undergo acetylation with acetyl chloride or acetic anhydride to form the corresponding acetate ester.
Alkylation: The nitrogen in the pyrimidine ring can act as a nucleophile and undergo alkylation reactions with alkyl halides or sulfonates.
Esterification: The hydroxyl group can react with carboxylic acids and acid chlorides to form ester derivatives.
Oxidation: The hydroxyl group can be oxidized to form the corresponding ketone or aldehyde, depending on the reaction conditions.
Nucleophilic Substitution: The pyrimidine ring can undergo nucleophilic substitution reactions with appropriate electrophiles.
Dehydration: Under certain conditions, dehydration reactions can occur, resulting in the elimination of water from the hydroxyl group.
Acylation: The nitrogen in the pyrimidine ring can undergo acylation reactions with acyl chlorides or acid anhydrides to form amide derivatives.
Condensation Reactions: The hydroxyl group may participate in condensation reactions with other compounds, leading to the formation of larger molecules.
Metalation: The pyrimidine ring may undergo metalation reactions with strong bases, leading to the formation of metal complexes.
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4,6-Dihydroxy-2-methylpyrimidine-5-carbaldehyde
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5-Bromo-2-methyl-6-(trifluoromethyl)pyrimidin-4-ol
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4-Hydroxy-2-methylpyrimidine-5-carbonitrile
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