Home Chemistry Heterocyclic Building Blocks Thiophenes 2-(Thiophen-2-Yl)Pyridine
Arylation or Alkylation: You can introduce substituents to the pyridine ring through electrophilic aromatic substitution. For example, you can react 2-(thiophen-2-yl)pyridine with aryl or alkyl halides in the presence of a suitable base or transition metal catalyst to add substituents to the pyridine ring.
Halogenation: 2-(thiophen-2-yl)pyridine can undergo halogenation reactions with halogenating agents like bromine or chlorine to introduce halogen atoms to the molecule.
Reduction: Reduction of the pyridine or thiophene ring can be achieved with reducing agents like hydrogen gas (catalytic hydrogenation) or with chemical reducing agents like lithium aluminum hydride (LiAlH4).
Oxidation: Oxidation of 2-(thiophen-2-yl)pyridine can be carried out with various oxidizing agents to convert it to the corresponding oxidation product.
Grignard Reaction: 2-(thiophen-2-yl)pyridine can react with Grignard reagents, which are organomagnesium compounds, to form new carbon-carbon bonds and introduce various functional groups.
Cross-Coupling Reactions: It can participate in various cross-coupling reactions like Suzuki-Miyaura, Heck, or Sonogashira reactions to form C-C bonds with other organic compounds.
Substitution Reactions: 2-(thiophen-2-yl)pyridine can undergo nucleophilic substitution reactions, especially with electrophilic functional groups.
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5-Bromo-2-(5-bromothiophen-2-yl)pyridine
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2-(5-Bromothiophen-2-yl)pyridine
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