Home Chemistry Heterocyclic Building Blocks Pyridines (3-Chloropyridin-2-Yl)Methanamine
Nucleophilic Substitution: The amino group can act as a nucleophile in substitution reactions. It can displace leaving groups on various electrophilic substrates.
Acylation: The amino group can undergo acylation reactions, where it reacts with acyl chlorides or acid anhydrides to form amides.
Alkylation: The amino group can undergo alkylation reactions with alkyl halides or other alkylating agents to form N-alkylated products.
Reductive Amination: The amine group can participate in reductive amination reactions, where it reacts with a carbonyl compound (aldehyde or ketone) in the presence of a reducing agent to form secondary or tertiary amines.
Ring Transformation: The pyridine ring can undergo various transformations, such as oxidation, reduction, or functional group modifications, depending on the reaction conditions and reagents used.
Heterocyclization: The amine group can participate in heterocyclization reactions to form heterocyclic compounds when reacted with suitable electrophiles.
Condensation Reactions: The amine group can undergo condensation reactions with carbonyl compounds to form imines or Schiff bases.
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(3-Chloro-6-methoxypyridin-2-yl)methanamine
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2-(Aminomethyl)-3-chloro-5-(trifluoromethyl)pyridine Hydrochloride
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(3-Chloro-5-fluoropyridin-2-yl)methanamine hydrochloride
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(3,5-Dichloropyridin-2-yl)methanamine dihydrochloride
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(3-Chloro-6-methoxypyridin-2-yl)methanamine dihydrochloride
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