Home Chemistry Heterocyclic Building Blocks Pyrrolidines 3-(Pyrrolidin-2-Yl)Pyridine
Acylation: You can react 3-(pyrrolidin-2-yl)pyridine with acyl chlorides or anhydrides to introduce acyl groups at the pyridine nitrogen or the pyrrolidine nitrogen.
Alkylation/Arylation: 3-(pyrrolidin-2-yl)pyridine can undergo nucleophilic substitution reactions with alkyl or aryl halides to introduce alkyl or aryl groups.
Reduction: You can reduce the carbonyl group to the corresponding alcohol using reducing agents like NaBH4 or LiAlH4.
Oxidation: You can oxidize the alcohol or other functional groups using suitable oxidizing agents like chromates or Jones reagent.
Ring-Opening Reactions: The pyrrolidine ring can undergo ring-opening reactions under various conditions, leading to the formation of open-chain compounds.
Condensation Reactions: It can participate in condensation reactions, such as the Knoevenagel condensation, to form C-C bonds.
Halogenation: You can halogenate the pyridine ring or the pyrrolidine ring using appropriate halogenating agents.
Cyclization: Depending on reaction conditions, it may undergo intramolecular reactions to form cyclic compounds.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
click to sign in and save
2-Methyl-3-(pyrrolidin-2-yl)pyridine dihydrochloride
click to sign in and save
tert-Butyl 2-(6-chloropyridin-3-yl)pyrrolidine-1-carboxylate
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :