Home Chemistry Heterocyclic Building Blocks Piperidines 3-Methoxypiperidine
Nucleophilic Substitution: The methoxy group can undergo nucleophilic substitution reactions with various electrophiles, leading to the formation of substituted ethers.
Alkylation: The nitrogen atom in the piperidine ring can be alkylated by reaction with alkyl halides or sulfonates.
Acylation: The nitrogen atom in the piperidine ring can undergo acylation reactions to form N-acyl derivatives.
Reduction: The nitro group can be reduced to the corresponding amine using reducing agents such as hydrogen gas over a metal catalyst or sodium borohydride.
Ring-opening Reactions: The piperidine ring may undergo ring-opening reactions under certain conditions, leading to the formation of linear or branched compounds.
Condensation Reactions: It can participate in condensation reactions with carbonyl compounds or other nucleophiles to form cyclic compounds or larger molecules.
Protonation: The amine group can be protonated under acidic conditions to form the corresponding ammonium salt.
Dehydration: Under appropriate conditions, dehydration reactions can occur to eliminate water and form unsaturated compounds.
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tert-Butyl 4-amino-3-methoxypiperidine-1-carboxylate
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(3S,4R)-tert-Butyl 4-amino-3-methoxypiperidine-1-carboxylate
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tert-Butyl (3S,4R)-4-amino-3-methoxypiperidine-1-carboxylate hydrochloride
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tert-Butyl cis-4-amino-3-methoxypiperidine-1-carboxylate hydrochloride
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