Chemistry Heterocyclic Building Blocks Pyrazoles 4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine
Ambeed provide 7 derivatives of 4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine.
These compounds have the same murcko framework: 4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine.
Alkylation: THPP can be alkylated by reaction with alkyl halides or alkylating agents, introducing alkyl groups onto the nitrogen atoms. This reaction often requires the use of a base or a catalyst.
Amination: THPP can undergo amination reactions to introduce amino groups. This can be achieved by using aminating agents like ammonia or amine compounds.
Oxidation: Depending on the reaction conditions, THPP may undergo oxidation to form oxidized derivatives. The exact products will depend on the oxidizing agent used.
Reduction: THPP can be reduced to produce saturated derivatives by using reducing agents such as hydrogen and a catalyst.
Cycloaddition: THPP may participate in cycloaddition reactions with suitable dienophiles or dipolarophiles to form fused ring compounds.
Substitution Reactions: THPP can undergo various substitution reactions at the carbon or nitrogen atoms, depending on the electrophilicity of the substituents.
Condensation: THPP may undergo condensation reactions with other compounds containing suitable functional groups, leading to the formation of new heterocyclic compounds.
Hydrolysis: Under acidic or basic conditions, THPP can undergo hydrolysis, leading to the cleavage of the ring and the formation of hydrolyzed products.
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3-(Trifluoromethyl)-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridine hydrochloride
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tert-Butyl 4,5-dihydro-1H-pyrazolo[3,4-c]pyridine-6(7H)-carboxylate
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4,5,6,7-Tetrahydro-1H-pyrazolo[3,4-c]pyridine dihydrochloride
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4,5,6,7-Tetrahydro-1H-pyrazolo[3,4-c]pyridine hydrochloride
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tert-Butyl 3-(trifluoromethyl)-4,5-dihydro-1H-pyrazolo[3,4-c]pyridine-6(7H)-carboxylate
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6-Boc-1,4,5,7-tetrahydropyrazolo[3,4-c]pyridine-3-carboxylic acid
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6-tert-Butyl 3-ethyl 4,5-dihydro-1H-pyrazolo[3,4-c]pyridine-3,6(7H)-dicarboxylate