Home Chemistry Heterocyclic Building Blocks Pyrrolidines Pyrrolidin-3-Ylmethanamine
Acylation: The nitrogen atom in the pyrrolidine ring can undergo acylation reactions to form N-acyl derivatives.
Alkylation: The nitrogen atom can be alkylated by reaction with alkyl halides or sulfonates.
Substitution Reactions: The nitrogen atom can undergo substitution reactions, such as nucleophilic 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.
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 amine and carboxylic acid.
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(R)-tert-Butyl 3-(aminomethyl)pyrrolidine-1-carboxylate
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tert-Butyl 3-(aminomethyl)pyrrolidine-1-carboxylate
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(S)-(1-Methylpyrrolidin-3-yl)methanamine
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(S)-1-Boc-3-Aminomethylpyrrolidine hydrochloride
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