Home Chemistry Heterocyclic Building Blocks Pyridines N-Methylpyridin-2-Amine
Nucleophilic substitution: The amine group can act as a nucleophile, replacing a leaving group in a substrate through a substitution reaction.
Acylation: The amine group can undergo acylation reactions, where it reacts with acyl halides or acid anhydrides to form amides.
Alkylation: The amine group can be alkylated with alkyl halides or sulfonates, forming N-alkylated products.
Reduction: The nitrogen in the amine group can be reduced to form secondary or tertiary amines, or even amines with a lower oxidation state.
N-oxidation: The nitrogen in the amine group can be oxidized to form N-oxide derivatives under appropriate conditions.
Heterocyclization: The pyridine ring can participate in various heterocyclization reactions, forming fused or non-fused heterocyclic compounds.
Condensation: The amine group can undergo condensation reactions with carbonyl compounds to form imines or enamines.
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N2-Methylpyridine-2,4-diamine hydrochloride
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3,5-Difluoro-N-methylpyridin-2-amine
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N2-Methylpyridine-2,5-diamine hydrochloride
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N2-Methylpyridine-2,5-diamine dihydrochloride
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5-(Aminomethyl)-N-methylpyridin-2-amine
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3-Chloro-N-methyl-5-(trifluoromethyl)pyridin-2-amine
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