2-(pyrrolidin-2-yl)pyridine-Pyrrolidines| Ambeed

Chemistry Heterocyclic Building Blocks Pyrrolidines 2-(pyrrolidin-2-yl)pyridine

2-(pyrrolidin-2-yl)pyridine

Ambeed provide 5 derivatives of 2-(pyrrolidin-2-yl)pyridine.

These compounds have the same murcko framework: 2-(pyrrolidin-2-yl)pyridine.

Nucleophilic Substitution: If there is a leaving group attached to the pyridine ring, you can perform nucleophilic substitution reactions. For example, you could replace a leaving group with another nucleophile.
Acylation: You can acylate the nitrogen atom in the pyrrolidine ring using acyl chlorides or anhydrides to introduce acyl groups.
Reductive Amination: You can perform reductive amination by reacting 2-(pyrrolidin-2-yl)pyridine with an amine and a reducing agent to introduce new amine groups.
Oxidation: The pyridine ring can undergo oxidation reactions to convert it into a different functional group, such as pyridine N-oxide.
Ring Opening Reactions: Depending on the conditions, you can induce ring-opening reactions of the pyrrolidine ring to form open-chain compounds or other cyclic structures.
Metal-Catalyzed Reactions: You can use transition metal catalysts to facilitate various reactions, such as cross-coupling reactions, C-H activation, and more.
Halogenation: You can halogenate the pyridine or pyrrolidine ring by using halogenating agents.
N-Heterocyclic Carbene Formation: Under appropriate conditions, 2-(pyrrolidin-2-yl)pyridine can be used as a precursor to create N-heterocyclic carbenes (NHCs), which are important ligands in organometallic chemistry.

2-(pyrrolidin-2-yl)pyridine

A111668886365-48-697%

$226.00/1g

A644607886365-52-295%

$910.00/1g

A14750032703756-57-295%

$303.00/100mg

A5497541803590-14-895+%

$228.00/100mg

A28057977790-61-598%

$163.00/1g