Home Chemistry Heterocyclic Building Blocks Pyridines 2,6-Dichloropyridine
Nucleophilic Substitution: The chlorine atoms on the pyridine ring can be replaced by nucleophiles such as hydroxide ions, amines, or thiolates, resulting in the formation of substituted pyridines.
Metalation: 2,6-dichloropyridine can undergo metalation reactions, where a metal atom replaces one of the chlorine atoms. This reaction is often performed using strong bases and can lead to the formation of organometallic complexes.
Reductive Dehalogenation: Under certain conditions, 2,6-dichloropyridine can undergo reductive dehalogenation reactions, leading to the removal of chlorine atoms and the formation of dihydropyridine derivatives.
Cross-Coupling Reactions: 2,6-dichloropyridine can participate in cross-coupling reactions, such as Suzuki-Miyaura or Heck reactions, where it reacts with suitable coupling partners in the presence of a catalyst to form biaryl or alkylated pyridine derivatives.
Aromatic Substitution: The electron-rich nature of the pyridine ring can undergo electrophilic aromatic substitution reactions, where electron-deficient species replace one of the hydrogen atoms on the ring. This can lead to the introduction of various functional groups onto the pyridine ring.
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2,6-Dichloro-N,N-dimethylpyridin-4-amine
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