Home Chemistry Heterocyclic Building Blocks Pyridines 5-Bromo-4-Methylpyridin-2-Amine
Substitution Reactions: The bromine atom can be substituted by another nucleophile, such as an amine, alcohol, or thiol group, through nucleophilic substitution reactions.
Amination Reactions: The amino group can undergo reactions with various electrophiles to form amine derivatives. For example, it can undergo acylation to form amides or alkylation to form N-alkylamines.
Cross-Coupling Reactions: The amino group can participate in cross-coupling reactions with aryl or alkyl halides, catalyzed by transition metals like palladium or copper, to form biaryl or diaryl compounds.
Reductive Amination: The amino group can react with carbonyl compounds in the presence of reducing agents to form secondary or tertiary amines.
Oxidation Reactions: The methyl group can undergo oxidation to form a carboxylic acid or ketone, depending on the conditions and reagents used.
Heterocycle Formation: The compound's pyridine ring can participate in various cyclization reactions to form fused or spiro heterocycles.
Amidation Reactions: The amino group can undergo amidation reactions with carboxylic acids or acid chlorides to form secondary or tertiary amides.
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2-Amino-5-bromo-4-methyl-3-nitropyridine
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2-Amino-5-bromo-4-methylnicotinonitrile
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