Chemistry Heterocyclic Building Blocks Pyridines 2,3-dihydro-1H-pyrrolo[3,4-c]pyridine
Ambeed provide 6 derivatives of 2,3-dihydro-1H-pyrrolo[3,4-c]pyridine.
These compounds have the same murcko framework: 2,3-dihydro-1H-pyrrolo[3,4-c]pyridine.
Ring Cleavage Reactions: The compound can be subjected to ring-opening reactions, where one of the rings in the fused system is cleaved. This can lead to the formation of open-chain compounds or compounds with a different ring system.
Alkylation and Acylation: The nitrogen atoms in the pyrrole and pyridine rings can undergo alkylation or acylation reactions. This can be achieved by reacting the compound with alkyl halides or acyl halides, respectively.
Reduction: The compound can be reduced to its corresponding dihydro product, which involves the addition of hydrogen atoms to the aromatic rings. This reduction can be catalytic or chemical, depending on the reaction conditions and reagents used.
Oxidation: Conversely, 2,3-dihydro-1H-pyrrolo[3,4-c]pyridine can be oxidized to produce the corresponding aromatic compound, which involves the removal of hydrogen atoms from the rings. Oxidizing agents like permanganates or chromates can be used for this purpose.
Substitution Reactions on Nitrogen Atoms: The nitrogen atoms in the pyrrole and pyridine rings can be further modified by various reactions, such as diazotization or substitution reactions with different functional groups.
Heterocyclic Chemistry: This compound can participate in various heterocyclic chemistry reactions, including reactions typical of pyridines and pyrroles, such as condensation reactions, rearrangements, and cyclizations.
Cross-Coupling Reactions: The compound can be used as a starting material in cross-coupling reactions, where it is coupled with other organic or organometallic compounds to form more complex molecules.
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Ethyl 1H-pyrrolo[3,4-c]pyridine-2(3H)-carboxylate
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2,3-Dihydro-1H-pyrrolo[3,4-c]pyridine dihydrochloride
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6-Chloro-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine hydrochloride
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2,3-Dihydro-1H-pyrrolo[3,4-c]pyridine hydrochloride
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6-Methyl-2,3-dihydro-1H-pyrrolo[3,4-c]pyridine dihydrochloride
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2,3-Dihydro-1H-pyrrolo[3,4-c]pyridine xhydrochloride