Home Chemistry Heterocyclic Building Blocks Piperidines 1-(Piperidin-4-Yl)Piperazine
N-Alkylation: 1-(piperidin-4-yl)piperazine has two nitrogen atoms that can undergo N-alkylation reactions. For example, you can react it with alkyl halides (e.g., methyl iodide) to form N-alkylated derivatives.
Acylation: It can undergo acylation reactions, where an acyl group (e.g., an acyl chloride or an anhydride) is introduced to one of the nitrogen atoms, forming an amide derivative.
Ring Opening: The piperazine rings can potentially undergo ring-opening reactions under certain conditions, leading to the formation of open-chain compounds.
Reduction: 1-(piperidin-4-yl)piperazine can be reduced using reducing agents such as lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4), which can convert the nitrogen atoms to amines.
Halogenation: Depending on the reaction conditions, it may be possible to halogenate the compound by treating it with halogenating agents such as bromine or iodine.
Oxidation: Under certain conditions, the compound can undergo oxidation reactions to form various oxidized products.
Condensation Reactions: 1-(piperidin-4-yl)piperazine can participate in condensation reactions with other compounds containing functional groups like aldehydes or ketones.
Heterocycle Formation: It can be used as a starting material in the synthesis of other heterocyclic compounds by reacting it with appropriate reagents.
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1-(Piperidin-4-yl)piperazine trihydrochloride
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1-Methyl-4-(piperidin-4-yl)piperazine trihydrochloride
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1-Methyl-4-(piperidin-4-yl)piperazine hydrochloride
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1-Ethyl-4-(piperidin-4-yl)piperazine hydrochloride
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