Home Chemistry Heterocyclic Building Blocks Piperidines 3-(Piperidin-4-Yl)-1H-Indazole
Acylation: The piperidine nitrogen is a potential site for acylation reactions. For example, you can react it with an acyl chloride or anhydride to form an amide derivative.
Reduction: The indazole ring may undergo reduction under certain conditions, typically with strong reducing agents like lithium aluminum hydride (LiAlH4) or sodium borohydride (NaBH4).
Oxidation: Indazole derivatives can be oxidized to form indazolones or other oxidized products using various oxidizing agents.
Heterocyclic Reactions: Depending on the conditions, 3-(piperidin-4-yl)-1H-indazole may undergo various heterocyclic reactions, such as ring-opening or ring-closing reactions.
Substitution Reactions: Like many aromatic compounds, indazoles can undergo electrophilic aromatic substitution reactions with appropriate electrophiles, such as nitration, halogenation, or Friedel-Crafts reactions.
Condensation Reactions: 3-(piperidin-4-yl)-1H-indazole can participate in condensation reactions with other compounds, leading to the formation of various heterocyclic or fused-ring systems.
Metalation: The indazole ring can be metalated with strong bases, allowing for further derivatization or reactions with electrophiles.
Cyclization: Depending on the reaction conditions and reagents, 3-(piperidin-4-yl)-1H-indazole may undergo cyclization reactions, forming different heterocyclic compounds.
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tert-Butyl 4-(1H-indazol-3-yl)piperidine-1-carboxylate
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tert-Butyl 4-(6-fluoro-1H-indazol-3-yl)piperidine-1-carboxylate
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tert-Butyl 4-(5-fluoro-1H-indazol-3-yl)piperidine-1-carboxylate
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tert-Butyl 4-(5-chloro-1H-indazol-3-yl)piperidine-1-carboxylate
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tert-Butyl 4-(5-bromo-1H-indazol-3-yl)piperidine-1-carboxylate
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