2-chloro-4-ethoxypyridine-Pyridines| Ambeed

: Nucleophilic Substitution: The sulfonamide group can be a target for nucleophilic substitution reactions. A nucleophile could attack the sulfur atom, leading to the displacement of the phenylsulfonyl group. Arylation or Alkylation: Depending on the reaction conditions, the imidazole ring might undergo arylation (replacement of an H with an aryl group) or alkylation (replacement of an H with an alkyl group). Acid-Base Reactions: The imidazole ring contains two nitrogen atoms that can act as bases. Depending on the pH of the environment, these nitrogens can potentially be protonated or deprotonated. Oxidation/Reduction Reactions: Under certain conditions, the compound might undergo oxidation or reduction reactions, especially if there are suitable oxidizing or reducing agents present. Metal Complexation: 1-(phenylsulfonyl)-1H-imidazole can potentially form coordination complexes with transition metals through its nitrogen atoms. Cross-Coupling Reactions: If subjected to appropriate conditions, it may undergo cross-coupling reactions with other organometallic compounds or aryl halides. Cyclization Reactions: Depending on the functional groups present, 1-(phenylsulfonyl)-1H-imidazole could participate in intramolecular reactions leading to the formation of cyclic compounds.

$397.00/25g