Home Chemistry Heterocyclic Building Blocks Pyrazoles 1-(Tetrahydro-2H-Pyran-4-Yl)-1H-Pyrazole
Alkylation: The compound can undergo alkylation reactions where alkyl halides or other alkylating agents react with the nitrogen in the pyrazole ring or the oxygen in the tetrahydro-2H-pyran ring.
Aldol Reaction: If there are appropriate functional groups nearby, an aldol reaction may occur, leading to the formation of a new carbon-carbon bond.
Oxidation: The tetrahydro-2H-pyran ring can be oxidized to form a corresponding ketone.
Reduction: The compound can undergo reduction reactions if there are suitable reducing agents present, potentially converting functional groups like ketones to alcohols.
Cyclization: Depending on the reaction conditions and the presence of other functional groups, intramolecular cyclization reactions can take place, leading to the formation of cyclic compounds.
Substitution Reactions: If there are leaving groups present on the compound, substitution reactions, such as nucleophilic aromatic substitution (SNAr) or other substitution reactions, can occur.
Grignard Reaction: The compound can react with Grignard reagents to form new carbon-carbon bonds.
Heterocyclic Chemistry: Given the presence of the pyrazole ring, it can participate in various heterocyclic chemistry reactions, including ring-opening and ring-closing reactions.
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4-Bromo-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazole
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5-Amino-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazole-4-carboxamide
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1-(Tetrahydro-2H-pyran-4-yl)-1H-pyrazol-5-amine
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4-Bromo-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazol-5-amine
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4-Bromo-3,5-dimethyl-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazole
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1-(Tetrahydro-2H-pyran-4-yl)-1H-pyrazole-4-carboxylic acid
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