Home Chemistry Heterocyclic Building Blocks Pyridines 3-Chloro-2-Fluoropyridine
Substitution Reactions: The chlorine and fluorine atoms on the pyridine ring can undergo substitution reactions with various nucleophiles or electrophiles, leading to the formation of different substituted pyridine derivatives.
Nucleophilic Aromatic Substitution (SNAr): The electron-deficient pyridine ring can undergo substitution reactions with nucleophiles such as amines, thiols, or alkoxides.
Metalation: The pyridine ring can be metalated using strong bases like butyllithium or sodium amide, leading to the formation of organometallic intermediates.
Cross-Coupling Reactions: The pyridine ring can undergo cross-coupling reactions with various coupling partners in the presence of transition metal catalysts, such as Suzuki, Heck, or Sonogashira reactions.
Reduction: The halogen substituents on the pyridine ring can be reduced to corresponding alkyl or hydrogen substituents under appropriate conditions.
Functional Group Transformations: Various functional groups can be introduced or modified on the pyridine ring through different chemical transformations such as oxidation, reduction, halogenation, or nitration.
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(5-Chloro-6-fluoropyridin-3-yl)boronic acid
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3-Chloro-2-fluoro-5-(trifluoromethyl)pyridine
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(3-Chloro-2-fluoropyridin-4-yl)boronic acid
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