Home Chemistry Heterocyclic Building Blocks Quinolines N-Phenyl-N-(4-(Quinolin-4-Yloxy)Phenyl)Cyclopropane-1,1-Dicarboxamide
Amide Hydrolysis: Treatment with strong acids or bases can hydrolyze the amide bonds in the molecule, leading to the cleavage of the amide groups into carboxylic acids and amines.
Aromatic Substitution: The phenyl and quinoline rings in the molecule are aromatic, making them susceptible to electrophilic aromatic substitution reactions. For example, reactions with electrophiles like halogens or nitration agents can lead to the substitution of hydrogen atoms in the aromatic rings.
Cyclopropane Ring Opening: The cyclopropane ring in the molecule can undergo ring-opening reactions under various conditions, such as treatment with strong acids or nucleophiles.
Reduction: The molecule contains multiple functional groups that can be reduced. For example, reduction of the nitro group to an amino group can be achieved using reducing agents like hydrogen and a metal catalyst.
Oxidation: The molecule contains several potentially oxidizable functional groups, such as the amine and alcohol groups, which can be oxidized using various oxidizing agents.
Nucleophilic Substitution: Depending on the reaction conditions, the amide and ether groups can undergo nucleophilic substitution reactions with appropriate nucleophiles.
Esterification: The carboxylic acid groups in the molecule can undergo esterification reactions with alcohols in the presence of acid catalysts.
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