Home Chemistry Heterocyclic Building Blocks Piperidines 1-(Methylsulfonyl)Piperidine
Nucleophilic Substitution: The sulfonyl group can undergo nucleophilic substitution reactions with various nucleophiles, leading to the displacement of the sulfonyl group.
Reduction: The sulfonyl group can be reduced to the corresponding sulfide or the amine using reducing agents such as sodium borohydride or hydrogen gas over a metal catalyst.
Substitution Reactions: The piperidine ring can undergo substitution reactions, such as nucleophilic substitution or electrophilic substitution.
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.
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.
Hydrolysis: The sulfonyl group can undergo hydrolysis under acidic or basic conditions to form the corresponding alcohols and sulfonic acids.
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1-(Methylsulfonyl)piperidine-4-carboxylic acid
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(1-(Methylsulfonyl)piperidin-4-yl)methanamine hydrochloride
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1-(Methylsulfonyl)piperidin-4-amine hydrochloride
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tert-Butyl (1-(methylsulfonyl)piperidin-4-yl)carbamate
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