Home Chemistry Heterocyclic Building Blocks Piperidines 1,3-Dihydrospiro[Indene-2,4'-Piperidine]
Aromatic Substitution: If there are electron-rich or electron-deficient substituents on the aromatic rings of the compound, it can undergo electrophilic aromatic substitution reactions. For example, it could react with electrophiles like bromine or nitric acid.
Reduction: The piperidine ring in the compound contains a potential site for reduction reactions. It could be reduced to the corresponding dihydroindene or even further to a saturated piperidine ring under certain conditions using reducing agents like hydrogen gas and a metal catalyst.
Nucleophilic Addition: If there are electrophilic sites within the molecule, it can undergo nucleophilic addition reactions. For example, if there is an electrophilic carbonyl group, it could react with nucleophiles like Grignard reagents or primary amines.
Oxidation: Depending on the specific functional groups present, the compound might be susceptible to oxidation reactions. Oxidizing agents like potassium permanganate or chromic acid could be used for such reactions.
Ring Opening: The piperidine ring can potentially undergo ring-opening reactions, especially if subjected to acidic or basic conditions. This could lead to the formation of open-chain compounds with various functional groups.
Cycloaddition: Depending on the reactivity of the molecule and the reaction conditions, it might be involved in various cycloaddition reactions, such as Diels-Alder reactions.
Substitution Reactions: If there are leaving groups present in the molecule, it could undergo substitution reactions with nucleophiles, such as nucleophilic substitution or SNAr reactions.
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(R)-N-((S)-1,3-Dihydrospiro[indene-2,4'-piperidin]-1-yl)-2-methylpropane-2-sulfinamide
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(S)-1,3-Dihydrospiro[indene-2,4'-piperidin]-1-amine dihydrochloride
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