Home Chemistry Heterocyclic Building Blocks Pyridines 5-Methylpyridin-2-Amine
Acylation: The amino group can undergo acylation reactions with acyl chlorides or acid anhydrides to form amides.
Alkylation: The amino group can be alkylated using alkyl halides or sulfonates, leading to N-alkylated products.
Acylation at the 5-position: The pyridine ring can undergo acylation reactions at the 5th position with acid chlorides or acid anhydrides, leading to amides.
Substitution Reactions: The pyridine ring can undergo electrophilic aromatic substitution reactions, such as nitration, halogenation, or sulfonation, depending on the reaction conditions and reagents used.
Reductive Amination: The amino group can undergo reductive amination reactions with carbonyl compounds in the presence of reducing agents to form secondary or tertiary amines.
Schiff Base Formation: The amino group can react with aldehydes or ketones to form Schiff bases.
Oxidation: The amino group can be oxidized to a nitro group under certain conditions.
Substitution at the Methyl Group: The methyl group can potentially undergo substitution reactions under specific reaction conditions.
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