Home Chemistry Heterocyclic Building Blocks Piperidines N-Phenylpiperidine-2-Carboxamide
Amide Hydrolysis: Under acidic or basic conditions, amide hydrolysis can occur, leading to the formation of N-phenylpiperidine-2-carboxylic acid.
Friedel-Crafts Acylation: If conditions are appropriate, N-phenylpiperidine-2-carboxamide can undergo acylation reactions, similar to the Friedel-Crafts acylation, which can introduce acyl groups onto the phenyl ring.
Substitution Reactions: The aromatic ring in the N-phenylpiperidine-2-carboxamide can undergo various substitution reactions, such as electrophilic aromatic substitution (EAS), to introduce different substituents on the phenyl group.
Redox Reactions: N-phenylpiperidine-2-carboxamide can be subjected to various redox reactions, such as oxidation or reduction, depending on the reaction conditions and reagents used.
Grignard Reaction: N-phenylpiperidine-2-carboxamide can react with a Grignard reagent, leading to the formation of new compounds through carbon-carbon bond formation.
Amide Coupling Reactions: It can participate in amide coupling reactions, such as the formation of amides with amines and suitable coupling agents like carbodiimides or acyl chlorides.
Catalytic Hydrogenation: Under the appropriate conditions and with a suitable catalyst, N-phenylpiperidine-2-carboxamide can undergo catalytic hydrogenation to reduce the amide group.
Reductive Cleavage: Depending on the reaction conditions, the amide bond can be selectively cleaved under reductive conditions to form different products.
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N-(2,6-Dimethylphenyl)piperidine-2-carboxamide hydrochloride
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