Chemistry Heterocyclic Building Blocks Pyrrolidines (R)-3-(pyrrolidin-2-yl)pyridine
Ambeed provide 9 derivatives of (R)-3-(pyrrolidin-2-yl)pyridine.
These compounds have the same murcko framework: (R)-3-(pyrrolidin-2-yl)pyridine.
Nucleophilic Substitution: The pyrrolidine nitrogen can act as a nucleophile, attacking electrophilic centers in other molecules. For example, it can react with alkyl halides to form N-alkylated pyrrolidines.
Acid-Base Reactions: The pyrrolidine nitrogen can act as a base, accepting a proton (H+) from an acidic compound.
Formation of Complexes: (R)-3-(pyrrolidin-2-yl)pyridine can coordinate with transition metals to form complexes. This can be useful in catalytic reactions.
Redox Reactions: Depending on the reaction conditions, it can undergo oxidation or reduction reactions, particularly if there are suitable reagents or catalysts present.
Esterification or Amidation: The pyridine ring can potentially participate in esterification or amidation reactions, where it reacts with carboxylic acids or acid chlorides to form esters or amides, respectively.
Alkylation or Acylation: The pyridine ring can also undergo alkylation or acylation reactions, where it reacts with alkyl halides or acyl chlorides to introduce substituents onto the ring.
Ring-Opening Reactions: Depending on the reaction conditions and reagents, the pyrrolidine ring might undergo ring-opening reactions, forming different compounds.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Formula Weight+−
click to sign in and save
(R)-3-(Pyrrolidin-2-yl)pyridine dihydrochloride
click to sign in and save
(R)-2-Methyl-3-(pyrrolidin-2-yl)pyridine dihydrochloride
click to sign in and save
(R)-2-chloro-5-fluoro-3-(pyrrolidin-2-yl)pyridine 2hcl
click to sign in and save
(R)-5-fluoro-2-methoxy-3-(pyrrolidin-2-yl)pyridine 2hcl
click to sign in and save
(R)-3-Fluoro-5-(pyrrolidin-2-yl)pyridine dihydrochloride
click to sign in and save
(R)-2-Methyl-5-(pyrrolidin-2-yl)pyridine dihydrochloride
click to sign in and save
(R)-3-Bromo-5-(pyrrolidin-2-yl)pyridine dihydrochloride