Home Chemistry Heterocyclic Building Blocks Pyrazoles 5-Cyclopropyl-1H-Pyrazole
Substitution Reactions: Depending on the substituents attached to the cyclopropyl and pyrazole rings, 5-cyclopropyl-1H-pyrazole can undergo nucleophilic substitution reactions. For example, if there is a halogen substituent (e.g., chlorine or bromine), it can undergo nucleophilic substitution with a nucleophile.
Acylation and Alkylation: 5-cyclopropyl-1H-pyrazole can react with acylating agents (e.g., acyl chlorides) to form amides or with alkylating agents to form alkyl derivatives.
Oxidation Reactions: Depending on the reaction conditions and functional groups present, oxidation reactions can occur. For example, it might be oxidized to form pyrazole oxides or other oxidation products.
Reduction Reactions: 5-cyclopropyl-1H-pyrazole can undergo reduction reactions with reducing agents to form reduced derivatives.
Cycloaddition Reactions: It can participate in cycloaddition reactions, such as Diels-Alder reactions, if the reaction conditions and substrates are appropriate.
Ring-Opening Reactions: Under certain conditions, the cyclopropyl ring can undergo ring-opening reactions, leading to the formation of open-chain compounds.
Condensation Reactions: It can participate in condensation reactions with suitable reagents to form new heterocyclic compounds.
Metal-Catalyzed Reactions: Transition metal catalysts can facilitate various reactions with 5-cyclopropyl-1H-pyrazole, such as cross-coupling reactions, C-H activation, and more.
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Methyl 5-cyclopropyl-1H-pyrazole-4-carboxylate
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5-Cyclopropyl-3-(trifluoromethyl)-1H-pyrazole
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