Home Chemistry Heterocyclic Building Blocks Pyrrolidines N-Methylpyrrolidin-3-Amine
Alkylation: The nitrogen atom can be further alkylated by reaction with alkyl halides or sulfonates.
Substitution Reactions: The nitrogen atom can undergo substitution reactions, such as nucleophilic substitution or electrophilic substitution.
Reduction: The imine group can be reduced to form the corresponding amine.
Condensation Reactions: It can participate in condensation reactions to form cyclic compounds or larger molecules.
Ring-opening Reactions: The pyrrolidine ring may undergo ring-opening reactions under certain conditions, leading to the formation of linear or branched compounds.
N-alkylation: The nitrogen atom can undergo alkylation reactions, where another alkyl group replaces the methyl group.
Oxidation: The amine group can be oxidized to form the corresponding imine or iminium ion.
Hydrolysis: Under acidic or basic conditions, amide bonds can undergo hydrolysis to regenerate the amines and carboxylic acids.
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(R)-tert-Butyl 3-(methylamino)pyrrolidine-1-carboxylate
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(S)-tert-Butyl 3-(methylamino)pyrrolidine-1-carboxylate
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tert-Butyl 3-(methylamino)pyrrolidine-1-carboxylate
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