Home Chemistry Heterocyclic Building Blocks Pyridines 6-Bromopyridin-2-Amine
Substitution Reactions: The bromine atom at position 6 can undergo substitution reactions with various nucleophiles, such as amines, alcohols, or thiols. This can lead to the formation of new compounds where the bromine atom is replaced by the nucleophile.
Amidation Reactions: The amino group can undergo amidation reactions with carboxylic acids or acyl chlorides to form amide compounds.
Condensation Reactions: The amino group can participate in condensation reactions with carbonyl compounds (such as aldehydes or ketones) to form imine or Schiff base compounds.
Metalation Reactions: The amino group can coordinate with metal ions, leading to metalation reactions. This can result in the formation of metal complexes or coordination compounds.
Redox Reactions: The compound can undergo redox reactions, especially involving the bromine atom, where it can be reduced or oxidized under appropriate conditions.
Acylation Reactions: The amino group can undergo acylation reactions with acyl halides or acid anhydrides to form amides.
Ring Closure Reactions: Depending on the reaction conditions and reagents, it may undergo ring closure reactions to form heterocyclic compounds.
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