Home Chemistry Heterocyclic Building Blocks Pyridines 6-Chloropyridine-3-Sulfonyl Chloride
Nucleophilic substitution: The chloride ion can be displaced by a nucleophile, such as a primary or secondary amine, to form a sulfonamide derivative.
Addition reactions: The sulfonyl chloride functional group can undergo addition reactions with nucleophiles, such as amines, alcohols, or thiols, to form sulfonamide, sulfonate ester, or sulfonate derivatives, respectively.
Friedel-Crafts acylation: 6-Chloropyridine-3-sulfonyl chloride can undergo Friedel-Crafts acylation with aromatic compounds in the presence of a Lewis acid catalyst, leading to the introduction of the sulfonyl group onto the aromatic ring.
Oxidation: It can undergo oxidation reactions under appropriate conditions to form sulfonyl compounds with higher oxidation states.
Reduction: It can undergo reduction reactions to yield sulfinyl or sulfanyl derivatives.
Substitution reactions: The chlorine atom can be substituted by various nucleophiles, such as amines, alcohols, or thiols, to introduce different functional groups onto the pyridine ring.
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