Home Chemistry Heterocyclic Building Blocks Piperazines Phenyl(Piperazin-1-Yl)Methanone
Acylation reactions: The nitrogen atoms could undergo acylation reactions with suitable acylating agents, forming amides.
Substitution reactions: The phenyl group can undergo various substitution reactions (e.g., halogenation, nitration, sulfonation) if suitable reagents are applied.
Ring-opening reactions: Depending on the conditions and reagents, the piperazine ring may undergo ring-opening reactions.
Condensation reactions: It could participate in condensation reactions with suitable nucleophiles or electrophiles.
Hofmann degradation: The amide functionality could be degraded under certain conditions, yielding a primary amine and a carbonyl compound.
Cyclization reactions: Depending on the reagents and conditions, the compound could potentially undergo cyclization reactions.
Formation of imine or enamine: The carbonyl group can react with a primary amine to form an imine or with a secondary amine to form an enamine.
Michael addition: The compound may participate in Michael addition reactions with suitable nucleophiles.
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tert-Butyl4-[4-(Aminomethyl)benzoyl]piperazine-1-carboxylate
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(2-Aminophenyl)(4-methylpiperazin-1-yl)methanone
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1-(2-Methoxybenzoyl)piperazine hydrochloride
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tert-Butyl 4-(3-iodobenzoyl)piperazine-1-carboxylate
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tert-Butyl 4-(3-bromobenzoyl)piperazine-1-carboxylate
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tert-Butyl 4-(4-aminobenzoyl)piperazine-1-carboxylate
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tert-Butyl 4-(4-nitrobenzoyl)piperazine-1-carboxylate
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(3-Bromophenyl)(4-methylpiperazin-1-yl)methanone
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(4-Nitrophenyl)(piperazin-1-yl)methanone
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1-(1,1-Dimethylethyl) 4-(4-boronobenzoyl)-1-piperazinecarboxylate
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