Home Chemistry Heterocyclic Building Blocks Pyrazoles 1-Cyclopentyl-1H-Pyrazole
Substitution Reactions: Like many aromatic compounds, 1-cyclopentyl-1H-pyrazole can undergo electrophilic aromatic substitution reactions. For example, it can react with strong electrophiles (e.g., acyl chlorides, nitration reagents) to substitute hydrogen atoms on the pyrazole ring with various functional groups.
Nucleophilic Substitution: If suitable leaving groups are present on the cyclopentyl or pyrazole ring, nucleophilic substitution reactions can occur. For instance, the compound can react with nucleophiles, such as amines or alkoxides, to replace a leaving group on the molecule.
Oxidation: 1-Cyclopentyl-1H-pyrazole can undergo oxidation reactions. Oxidizing agents can convert it into compounds with more oxygen atoms, depending on the conditions. Oxidation could lead to the formation of pyrazole N-oxides or other oxygen-containing functional groups.
Reduction: The compound can also be reduced under suitable conditions, converting functional groups to more reduced forms. For example, reduction with strong reducing agents can lead to the formation of the corresponding amines or even fully reduced derivatives.
Acylation: 1-Cyclopentyl-1H-pyrazole can undergo acylation reactions, where acyl groups are added to the molecule. This is often achieved by reacting it with acyl halides or anhydrides in the presence of a base.
Alkylation: Alkylation reactions can be carried out by reacting 1-cyclopentyl-1H-pyrazole with alkylating agents in the presence of a base. This can result in the introduction of alkyl groups onto the pyrazole ring.
Condensation Reactions: Depending on the functional groups present, 1-cyclopentyl-1H-pyrazole can participate in condensation reactions to form larger molecules. For instance, it can undergo a Mannich reaction when treated with formaldehyde and a primary or secondary amine.
Metalation: The pyrazole ring can serve as a ligand for various metal ions. Reactions with metal ions can lead to the formation of coordination complexes, which may have unique properties and reactivities.
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Ethyl 1-cyclopentyl-5-hydroxy-1H-pyrazole-4-carboxylate
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3-Amino-1-cyclopentyl-1H-pyrazole-4-carbonitrile
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4-Bromo-1-cyclopentyl-3-(trifluoromethyl)-1H-pyrazole
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(1-Cyclopentyl-3-(trifluoromethyl)-1H-pyrazol-4-yl)boronic acid
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