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CAS 1001635-01-3

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(3S,4S)-3-Amino-4-methoxy-pyrrolidine-1-carboxylic acid tert-butyl ester

Description:
(3S,4S)-3-Amino-4-methoxy-pyrrolidine-1-carboxylic acid tert-butyl ester is a chiral compound characterized by its pyrrolidine ring structure, which includes an amino group and a carboxylic acid moiety. The presence of the tert-butyl ester group enhances its lipophilicity, making it more soluble in organic solvents compared to its free acid form. This compound is typically used in the synthesis of various pharmaceuticals and bioactive molecules due to its ability to serve as a building block in organic synthesis. The specific stereochemistry, denoted by the (3S,4S) configuration, is crucial for its biological activity, as stereoisomers can exhibit significantly different properties and interactions in biological systems. Additionally, the methoxy group contributes to the compound's overall polarity and can influence its reactivity and interaction with other chemical entities. Overall, this compound exemplifies the importance of stereochemistry and functional group manipulation in the design of biologically relevant molecules.
Formula:C10H20N2O3
Synonyms:
  • (3S,4S)-3-Amino-4-methoxy-pyrrolidine-1-carboxylic acid tert-butyl ester
  • (3S,4S)-3-Amino-1-Boc-4-methoxypyrrolidine
  • 1-Pyrrolidinecarboxylic acid, 3-amino-4-methoxy-, 1,1-dimethylethyl ester, (3S,4S)-
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