Chemistry Heterocyclic Building Blocks Imidazoles 8-methylimidazo[1,2-a]pyridine
Ambeed provide 9 derivatives of 8-methylimidazo[1,2-a]pyridine.
These compounds have the same murcko framework: 8-methylimidazo[1,2-a]pyridineSubstitution Reactions: The methyl group at the 8-position could potentially undergo substitution reactions. For example, it might be replaced by another functional group in the presence of appropriate reagents.
Aromatic Electrophilic Substitution: The aromatic nature of the imidazo[1,2-a]pyridine ring suggests that it might undergo electrophilic aromatic substitution reactions. This could involve the introduction of various substituents under the influence of electrophiles.
Reduction Reactions: The imine nitrogen in the imidazo[1,2-a]pyridine ring might be reducible, leading to the formation of a saturated derivative, such as a dihydroimidazo[1,2-a]pyridine.
Nucleophilic Substitution: Depending on the reaction conditions, nucleophiles could potentially substitute other atoms or groups within the molecule.
Metalation Reactions: The imidazo[1,2-a]pyridine ring might be susceptible to metalation reactions, where a metal atom replaces a hydrogen atom on the ring.
Oxidation Reactions: The methyl group or other functional groups within the molecule might be oxidizable under certain conditions.
Condensation Reactions: Depending on the presence of suitable functional groups, 8-methylimidazo[1,2-a]pyridine might participate in condensation reactions to form larger cyclic or acyclic structures.
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2-(Chloromethyl)-8-methylimidazo[1,2-a]pyridine
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6-Bromo-2,3,8-trimethylimidazo[1,2-a]pyridine
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3-Iodo-8-methylimidazo[1,2-a]pyridine
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6-Bromo-2-ethyl-N,8-dimethylimidazo[1,2-a]pyridin-3-amine
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2,8-Dimethylimidazo[1,2-a]pyridine-3-carboxylic acid