Home Chemistry Heterocyclic Building Blocks Piperazines 3-(Piperazin-1-Yl)Pyridazine
Alkylation: 3-(piperazin-1-yl)pyridazine can undergo alkylation reactions with alkyl halides or alkylating agents in the presence of a base to form N-alkylated derivatives.
Acylation: The compound can be acylated by reacting it with acyl chlorides or anhydrides in the presence of a base to introduce acyl groups to the piperazine nitrogen.
Nucleophilic Substitution: The compound can participate in nucleophilic substitution reactions, where a nucleophile can replace a functional group or atom, depending on the reaction conditions.
Reductive Amination: Reductive amination reactions can be employed to introduce various amine groups to the piperazine nitrogen in the presence of a reducing agent like sodium cyanoborohydride.
Oxidation: 3-(piperazin-1-yl)pyridazine can be oxidized under appropriate conditions, leading to the formation of various oxidation products.
Formation of Complexes: It can also form complexes with metal ions, which can have various applications in coordination chemistry.
Cyclization: Depending on the reaction conditions, it can undergo cyclization reactions to form cyclic compounds.
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1-Boc-4-(6-Chloropyridazin-3-yl)piperazine
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6-(4-Methylpiperazin-1-yl)pyridazin-3-amine
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tert-Butyl 4-(pyridazin-3-yl)piperazine-1-carboxylate
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3-Chloro-6-(piperazin-1-yl)pyridazine hydrochloride
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3-Bromo-6-(4-methylpiperazin-1-yl)pyridazine
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