Home Chemistry Heterocyclic Building Blocks Pyrrolidines Pyrrolidin-2-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 sulfonatesl.
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.
Oxidation: The amine group can be oxidized to form the corresponding imine or iminium ion.
Hydrolysis: Under acidic or basic conditions, amine bonds can undergo hydrolysis to regenerate the amines and carboxylic acids.
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(R)-Pyrrolidin-2-ylmethanamine dihydrochloride
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(R)-tert-Butyl 2-(aminomethyl)pyrrolidine-1-carboxylate hydrochloride
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(S)-Pyrrolidin-2-ylmethanamine dihydrochloride
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(S)-(1-Methylpyrrolidin-2-yl)methanamine dihydrochloride
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(R)-(1-(Methylsulfonyl)pyrrolidin-2-yl)methanamine
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(R)-(1-Methylpyrrolidin-2-yl)methanamine
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(S)-tert-Butyl 2-(aminomethyl)pyrrolidine-1-carboxylate hydrochloride
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