Home Chemistry Heterocyclic Building Blocks Pyridines 4-(2,4-Diphenyl-1H-Imidazol-5-Yl)Pyridine
Hydrogenation: You can perform hydrogenation reactions to reduce the double bonds in the phenyl rings or the imidazole ring. This typically requires the use of a catalyst, such as palladium on carbon (Pd/C), and hydrogen gas H2.
Bromination or Chlorination: You can brominate or chlorinate this compound by using a brominating or chlorinating agent, respectively, to introduce bromine or chlorine atoms into the molecule.
Acylation or Alkylation: The nitrogen atoms in the imidazole ring are potential sites for acylation or alkylation reactions. You can introduce acyl or alkyl groups to these nitrogen atoms using appropriate reagents.
Oxidation and Reduction: Depending on the reaction conditions, you can oxidize or reduce specific functional groups within the molecule. For instance, you can oxidize the alcohol group to a ketone or reduce a carbonyl group to an alcohol using suitable reagents.
Grignard Reaction: You can prepare Grignard reagents and react them with this compound to form new carbon-carbon bonds. This can be useful for synthetic purposes.
Heterocyclization: You can use this molecule as a starting material for various heterocyclization reactions to form different heterocyclic compounds.
Cross-Coupling Reactions: If you have suitable functional groups, you can perform cross-coupling reactions, such as Suzuki-Miyaura or Heck reactions, to introduce aryl or alkyl groups at specific positions in the molecule.
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