Home Chemistry Heterocyclic Building Blocks Benzimidazoles 2-((Pyridin-2-Ylmethyl)Thio)-1H-Benzo[D]Imidazole
Alkylation: It can undergo alkylation reactions with alkyl halides or alkylating agents to form alkylated derivatives. This might involve substitution of the hydrogen atom on the nitrogen or sulfur atoms.
Reduction: The compound could undergo reduction reactions with reducing agents like lithium aluminum hydride (LiAlH4) to form reduced derivatives.
Aromatic Substitution: Depending on the reaction conditions, it might undergo electrophilic aromatic substitution reactions at the aromatic rings, such as halogenation, nitration, or Friedel-Crafts reactions.
Nucleophilic Substitution: It might undergo nucleophilic substitution reactions at positions that are susceptible to nucleophilic attack. The nitrogen or sulfur atoms could act as nucleophilic centers.
Metalation: It could react with certain metal reagents, like organolithium compounds or Grignard reagents, leading to the formation of organometallic compounds.
Cyclization: The compound's structure may promote intramolecular reactions, leading to the formation of cyclic compounds.
Cross-Coupling Reactions: It could participate in cross-coupling reactions with various coupling partners to form biaryl compounds.
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6-Methyl-2-(((3-methyl-4-(2,2,2-trifluoroethoxy)pyridin-2-yl)methyl)thio)-1H-benzo[d]imidazole
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2-(((6-(Difluoromethoxy)-1H-benzo[d]imidazol-2-yl)thio)methyl)-3,4-dimethoxypyridine 1-oxide
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2-(((3-Methyl-4-(2,2,2-trifluoroethoxy)pyridin-2-yl)methyl)thio)-1H-benzo[d]imidazole hydrate
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