Home Chemistry Heterocyclic Building Blocks Pyridazines [1,2,4]Triazolo[4,3-B]Pyridazine
Substitution Reactions: [1,2,4]triazolo[4,3-b]pyridazine contains multiple nitrogen atoms that can undergo nucleophilic substitution reactions with various electrophiles. For example, you can perform N-alkylation or N-acylation reactions to introduce alkyl or acyl groups at the nitrogen atoms.
Cycloaddition Reactions: [1,2,4]triazolo[4,3-b]pyridazine can participate in various cycloaddition reactions. For instance, it can undergo Diels-Alder reactions with appropriate dienes and dienophiles to form fused ring systems.
Oxidation and Reduction Reactions: The aromatic ring in [1,2,4]triazolo[4,3-b]pyridazine can undergo oxidation or reduction reactions, depending on the reaction conditions and reagents used. These reactions can lead to the formation of different functionalized derivatives.
Condensation Reactions: [1,2,4]triazolo[4,3-b]pyridazine can participate in condensation reactions with suitable carbonyl compounds, leading to the formation of imine or enamine derivatives.
Metal-Catalyzed Reactions: Transition metal catalysts can be used to facilitate various transformations of [1,2,4]triazolo[4,3-b]pyridazine, including C-C bond formation, C-N bond formation, and other metal-catalyzed reactions.
Functional Group Transformations: The functional groups present in [1,2,4]triazolo[4,3-b]pyridazine can be modified through a wide range of reactions, including halogenation, hydroxylation, amination, and more.
Ring Opening Reactions: Depending on the conditions and reagents, [1,2,4]triazolo[4,3-b]pyridazine can undergo ring-opening reactions, leading to the formation of open-chain derivatives.
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(6-Chloro-[1,2,4]triazolo[4,3-b]pyridazin-3-yl)methanamine hydrochloride
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Ethyl 6-chloro-[1,2,4]triazolo[4,3-b]pyridazine-3-carboxylate
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tert-Butyl (6-chloro-3-methyl-[1,2,4]triazolo[4,3-b]pyridazin-8-yl)carbamate
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6-Chloro-3-methyl-[1,2,4]triazolo[4,3-b]pyridazine
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3-Chloro-6-methyl-[1,2,4]triazolo[4,3-b]pyridazine
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3,6-Dichloro-[1,2,4]triazolo[4,3-b]pyridazine
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6-Chloro-3-methyl-[1,2,4]triazolo[4,3-b]pyridazin-8-amine
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