Home Chemistry Heterocyclic Building Blocks Pyridines 2-Methoxy-5-Methylpyridine
Electrophilic aromatic substitution: The electron-rich aromatic ring can undergo substitution reactions with electrophiles, such as halogens or acyl groups, to yield substituted products.
Nucleophilic substitution: The methoxy group can be displaced by nucleophiles under suitable conditions.
Acylation: The nitrogen atom in the pyridine ring can undergo acylation reactions with acyl halides or acid acid anhydrides to form amides.
Reduction: The nitro group can be reduced to an amine under appropriate reaction conditions.
Oxidation: The methyl group can be oxidized to a carboxylic acid or aldehyde depending on the reaction conditions and reagents used.
Heterocyclization: The compound can undergo reactions to form fused heterocyclic compounds under suitable conditions.
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(2-Methoxy-5-methylpyridin-3-yl)boronic acid
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