3-(piperidin-1-yl)pyridine-Piperidines| Ambeed

Chemistry Heterocyclic Building Blocks Piperidines 3-(piperidin-1-yl)pyridine

3-(piperidin-1-yl)pyridine

Ambeed provide 5 derivatives of 3-(piperidin-1-yl)pyridine.

These compounds have the same murcko framework: 3-(piperidin-1-yl)pyridine.

Acylation: 3-(piperidin-1-yl)pyridine can undergo acylation reactions, where an acyl group (RCO-) replaces a hydrogen atom on the piperidine or pyridine ring. Common reagents for acylation reactions include acyl chlorides or anhydrides.
Alkylation: Alkylation reactions involve the introduction of alkyl groups onto the piperidine or pyridine ring. This can be achieved using alkyl halides or alkyl sulfonates in the presence of a suitable base.
Reduction: Reduction reactions can be used to convert any functional groups with double bonds or other reducible groups to their corresponding saturated forms. Common reducing agents like lithium aluminum hydride (LiAlH₄) or sodium borohydride (NaBH₄) can be employed.
Halogenation: Halogenation reactions involve the substitution of hydrogen atoms with halogen atoms (chlorine, bromine, etc.) on the piperidine or pyridine ring. This can be accomplished using appropriate halogenating agents.
Oxidation: Oxidation reactions can be used to convert certain functional groups to their oxidized forms. Common oxidizing agents include potassium permanganate (KMnO₄) or chromium(VI) reagents.
Ring Opening: The piperidine ring can undergo ring-opening reactions under specific conditions. This can lead to the formation of compounds with open-chain structures.
Substitution Reactions: Depending on the reaction conditions and reagents used, 3-(piperidin-1-yl)pyridine can undergo various substitution reactions, such as nucleophilic substitution, electrophilic substitution, or radical substitution.

3-(piperidin-1-yl)pyridine

A2381021619264-47-995%

$18.00/100mg

A2205471335058-51-995%

$46.00/250mg

A117911878742-33-795%

$116.00/1g

A7543991142197-44-197%

$195.00/1g

A230136847406-13-797%

$29.00/50mg