Home Chemistry Heterocyclic Building Blocks Pyridines 2,6-Dichloronicotinonitrile
Substitution Reactions: The chlorine atoms on the pyridine ring can undergo substitution reactions with other nucleophiles. For example, they can be replaced by other halogens, such as bromine or iodine, or by alkyl or aryl groups.
Nucleophilic Addition Reactions: The cyano group (-CN) can undergo nucleophilic addition reactions, where a nucleophile adds to the carbon atom of the cyano group. This could lead to the formation of amines or other functional groups depending on the reaction conditions.
Reduction Reactions: The cyano group can be reduced to form primary amines using reducing agents such as lithium aluminum hydride (LiAlH4) or hydrogen gas in the presence of a catalyst.
Grignard Reactions: 2,6-dichloronicotinonitrile can undergo Grignard reactions where the cyano group is converted into a ketone after reaction with a Grignard reagent.
Metal-Catalyzed Cross-Coupling Reactions: The halogen atoms can undergo cross-coupling reactions with organometallic reagents (such as organolithium or organomagnesium compounds) in the presence of a transition metal catalyst to form biaryl compounds.
Ring-Opening Reactions: Under certain conditions, the pyridine ring may undergo ring-opening reactions, leading to the formation of open-chain compounds.
Oxidation Reactions: The compound can undergo oxidation reactions, for example, the oxidation of the cyano group to a carboxylic acid or other oxidized functional groups.
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Methyl 2-(2,6-dichloro-3-cyanopyridin-4-yl)acetate
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2,6-Dichloro-5-(trifluoromethyl)nicotinonitrile
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2,6-Dichloro-4-isopropylnicotinonitrile
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2,6-Dichloro-4-(difluoromethyl)nicotinonitrile
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2,6-Dichloro-4-(trifluoromethyl)nicotinonitrile
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