Home Chemistry Heterocyclic building blocks Piperidines 4-hydrazineylpiperidine
Schiff Base Formation: The hydrazine group can react with carbonyl compounds to form Schiff bases, particularly under acidic conditions.
Nucleophilic Substitution: The hydrazine group can undergo nucleophilic substitution reactions with various electrophiles, such as alky halides or acyl chlorides, to form substituted hydrazines.
Hydrazine Derivative Formation: The hydrazine group can react with ketones or aldehydes to form hydrazones.
Oxidation: The hydrazine group can be oxidized to form the corresponding diazo compound or azo compound under suitable conditions.
Condensation Reactions: It can participate in condensation reactions with carbonyl compounds or other nucleophiles to form cyclic compounds or larger molecules.
Acylation: The nitrogen atom in the piperidine ring can undergo acylation reactions to form N-acyl derivatives.
Reduction: The nitrogen-nitrogen bond can be reduced to form hydrazines using reducing agents such as sodium borohydride or hydrogen gas over a metal catalyst.
Amidation: The hydrazine group can react with carboxylic acids or acid derivatives to form amides.
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4-Hydrazinyl-1-methylpiperidine hydrochloride
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tert-Butyl 4-hydrazinylpiperidine-1-carboxylate oxalate
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tert-Butyl 4-hydrazinylpiperidine-1-carboxylate hydrochloride
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4-Hydrazinyl-1-methylpiperidine dihydrochloride
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4-Hydrazinylpiperidine dihydrochloride
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