Home Chemistry Heterocyclic building blocks Pyrazoles 3-cyclopropyl-1h-pyrazole
Substitution Reactions: Depending on the specific substituents on the cyclopropyl-1H-pyrazole, it may undergo various substitution reactions, including electrophilic aromatic substitution, nucleophilic substitution, or radical substitution.
Acylation: The nitrogen atoms in the pyrazole ring can undergo acylation reactions, typically with acyl halides or anhydrides to form amides.
Alkylation: The nitrogen atoms in the pyrazole ring can also be alkylated using alkyl halides, providing N-alkylated pyrazoles.
Ring-Opening Reactions: The cyclopropane ring in the cyclopropyl group can potentially undergo ring-opening reactions under certain conditions.
Oxidation and Reduction: Depending on the reaction conditions, it can undergo oxidation or reduction reactions, typically with strong oxidizing or reducing agents, respectively.
Condensation Reactions: If there are suitable functional groups, it may undergo condensation reactions with other compounds, forming new cyclic or acyclic products.
Cycloaddition Reactions: Depending on the reagents and conditions, it might participate in cycloaddition reactions like [3+2] cycloadditions, which are common for pyrazole compounds.
Isomerization: Depending on the substituents, it may undergo isomerization reactions, such as tautomerization.
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3-Cyclopropyl-4-methyl-1H-pyrazole-5-carboxylic acid
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3-Cyclopropyl-1H-pyrazol-5-amine hydrochloride
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Ethyl 3-Cyclopropylpyrazole-4-carboxylate
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