Chemistry Heterocyclic Building Blocks Imidazoles 4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine
Ambeed provide 5 derivatives of 4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine.
These compounds have the same murcko framework: 4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine.
Acylation: The nitrogen atom in the imidazole ring can undergo acylation reactions, where it can be reacted with acyl chlorides or anhydrides to form amides.
Alkylation: The nitrogen atom in the imidazole ring can also undergo alkylation reactions, where it can be reacted with alkyl halides or alkylating agents to form alkylated derivatives.
Oxidation: Depending on the reaction conditions, the compound may undergo oxidation reactions, potentially leading to the formation of various oxidation products.
Reduction: Under certain conditions, the compound can be reduced to form saturated derivatives. For example, reduction with hydrogen gas and a suitable catalyst could lead to the formation of a saturated tetrahydro-imidazo[4,5-c]pyridine.
Substitution: Substitution reactions can occur at various positions on the heterocyclic ring. For example, nucleophilic substitution can replace a leaving group with a nucleophile.
Ring-opening reactions: Under specific conditions, the ring structure of imidazo[4,5-c]pyridine can undergo ring-opening reactions to form open-chain compounds.
Cyclization: In some cases, this compound can participate in intramolecular cyclization reactions to form other cyclic compounds.
Condensation reactions: Depending on the functional groups present, 4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine can participate in condensation reactions with other compounds, leading to the formation of new compounds.
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5-Methyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine dihydrochloride
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2-Methyl-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine hydrochloride
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4,5,6,7-Tetrahydro-3H-imidazo[4,5-c]pyridine hydrochloride
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4,5,6,7-Tetrahydro-3H-imidazo[4,5-c]pyridine dihydrochloride
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(S)-4,5,6,7-Tetrahydro-3H-imidazo[4,5-c]pyridine-6-carboxylic acid hydrochloride