Home Chemistry Heterocyclic Building Blocks Pyridines 2-(1H-Pyrazol-3-Yl)Pyridine
Substitution Reactions: The pyridine ring can undergo substitution reactions, such as electrophilic aromatic substitution. For example, you can react it with various electrophiles to introduce different functional groups at the pyridine ring.
Nucleophilic Substitution: The pyrazole ring can undergo nucleophilic substitution reactions, where the pyrazole nitrogen can act as a nucleophile to react with electrophiles.
Metal Complexation: The nitrogen atoms in both the pyridine and pyrazole rings can coordinate with transition metal ions, forming metal complexes. This can be useful in catalytic reactions or for the synthesis of organometallic compounds.
Condensation Reactions: 2-(1H-pyrazol-3-yl)pyridine can be involved in condensation reactions with other compounds, leading to the formation of new compounds.
Oxidation and Reduction Reactions: The compound can undergo oxidation or reduction reactions, depending on the reaction conditions and reagents used.
Grignard Reactions: You can react 2-(1H-pyrazol-3-yl)pyridine with a Grignard reagent to introduce various organic groups onto the molecule.
Acylation and Alkylation: The compound can undergo acylation or alkylation reactions, which can modify the pyridine or pyrazole ring.
Hydrogenation: You can carry out hydrogenation reactions to reduce the double bonds in the compound.
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Methyl 3-(pyridin-2-yl)-1H-pyrazole-5-carboxylate
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