Chemistry
Heterocyclic Building Blocks
Pyrrolidines
(S)-N-phenethyl-3-(pyrrolidin-2-yl)propanamide
Hydrolysis: The amide bond in the compound can undergo hydrolysis in acidic or basic conditions to yield (S)-phenethylamine and 3-(pyrrolidin-2-yl)propanoic acid.
Acylation: The amine group can be acylated with different acylating agents (e.g., acyl chlorides, anhydrides) to form amide derivatives.
Reductive Amination: The compound can undergo reductive amination with various carbonyl compounds and reducing agents to form secondary amines.
Oxidation: The compound can be oxidized to form corresponding carboxylic acids or other oxidized derivatives.
Reduction: The carbonyl group can be reduced to the corresponding alcohol using reducing agents like sodium borohydride or lithium aluminum hydride.
Alkylation: The amine group can be alkylated using alkyl halides or other alkylating agents.
Substitution Reactions: The compound may undergo substitution reactions at the aromatic ring or other reactive positions depending on the reaction conditions and reagents used.
Cyclization Reactions: Depending on the reaction conditions, the compound may undergo cyclization reactions to form cyclic derivatives.
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