Home Chemistry Heterocyclic Building Blocks Pyrrolidines 2-Methylpyrrolidine
N-Methylation: The nitrogen atom can undergo methylation reactions, where a methyl group is added to the nitrogen atom.
Substitution Reactions: The nitrogen atom can undergo substitution reactions, such as nucleophilic substitution or electrophilic substitution.
Ring-opening Reactions: The pyrrolidine ring may undergo ring-opening reactions under certain conditions, leading to the formation of linear or branched compounds.
Alkylation: The nitrogen atom can be further alkylated by reaction with alkyl halides or sulfonates.
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.
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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tert-Butyl ((3S,5R)-5-methylpyrrolidin-3-yl)carbamate
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tert-Butyl ((3R,5S)-5-methylpyrrolidin-3-yl)carbamate
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(2S,5R)-N-Boc-5-methylpyrrolidine-2-carboxylic acid
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2-Methylpyrrolidine-1-sulfonyl chloride
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(R)-tert-Butyl 2-methylpyrrolidine-1-carboxylate
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(2R,4S)-tert-Butyl 4-hydroxy-2-methylpyrrolidine-1-carboxylate
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(2R,4S)-tert-Butyl 4-amino-2-methylpyrrolidine-1-carboxylate
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(2R,4R)-tert-Butyl 4-amino-2-methylpyrrolidine-1-carboxylate
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(S)-tert-Butyl 2-methylpyrrolidine-1-carboxylate
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(2S,4S)-tert-Butyl 4-hydroxy-2-methylpyrrolidine-1-carboxylate
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cis-tert-Butyl 4-hydroxy-2-methylpyrrolidine-1-carboxylate
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(2S,4R)-tert-Butyl 4-hydroxy-2-methylpyrrolidine-1-carboxylate
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trans-2,5-Dimethylpyrrolidine hydrochloride
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