Home Chemistry Heterocyclic Building Blocks Pyridines 5-Bromopicolinonitrile
Substitution Reactions: The bromine atom in 5-bromopicolinonitrile can undergo substitution reactions, where it is replaced by other nucleophiles. For instance, substitution with another nucleophile such as hydroxide ion (OH⁻) can lead to the formation of 5-hydroxypicolinonitrile.
Nucleophilic Addition Reactions: The nitrile group (−C≡N) can undergo nucleophilic addition reactions. For example, reaction with a strong nucleophile such as sodium azide (NaN3) can lead to the formation of the corresponding azide compound.
Reduction Reactions: The nitrile group can undergo reduction to yield primary amines. For instance, reduction with lithium aluminum hydride (LiAlH4) can yield the corresponding primary amine.
Cross-Coupling Reactions: 5-Bromopicolinonitrile can undergo cross-coupling reactions, such as Suzuki coupling or Heck coupling, to form biaryl compounds or substituted pyridine derivatives.
Acylation Reactions: The nitrile group can be converted to an amide group via acylation reactions. For example, reaction with an acyl chloride in the presence of a base can yield the corresponding amide.
Oxidation Reactions: The compound can undergo oxidation reactions under appropriate conditions, leading to the formation of various oxidized products.
Halogenation Reactions: The pyridine ring can undergo halogenation reactions under specific conditions, introducing halogen atoms at different positions on the ring.
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5-Bromo-3-methoxypyridine 2-carbonitrile
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5-Bromo-3-(trifluoromethyl)-2-pyridinecarbonitrile
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