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CAS 131878-23-4

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(3R)-(+)-1-Benzyl-3-(Tert-Butoxycarbonylamino)Pyrrolidine

Description:
(3R)-(+)-1-Benzyl-3-(Tert-Butoxycarbonylamino)Pyrrolidine is a chiral organic compound characterized by its pyrrolidine backbone, which is a five-membered nitrogen-containing heterocycle. The presence of a benzyl group enhances its hydrophobic characteristics, while the tert-butoxycarbonyl (Boc) group serves as a protective moiety for the amino group, making it useful in peptide synthesis and other organic transformations. This compound is typically utilized in the field of medicinal chemistry and drug development due to its potential biological activity. Its chirality, indicated by the (3R) configuration, is crucial for its interaction with biological targets, as stereochemistry can significantly influence pharmacodynamics and pharmacokinetics. The compound is generally stable under standard laboratory conditions but may require specific handling to maintain its integrity, particularly in the presence of strong acids or bases that could hydrolyze the Boc group. Overall, (3R)-(+)-1-Benzyl-3-(Tert-Butoxycarbonylamino)Pyrrolidine is a valuable intermediate in the synthesis of various pharmaceutical agents.
Formula:C16H24N2O2
InChI:InChI=1/C16H24N2O2/c1-16(2,3)20-15(19)17-14-9-10-18(12-14)11-13-7-5-4-6-8-13/h4-8,14H,9-12H2,1-3H3,(H,17,19)
Synonyms:
  • (R)-(+)-1-Benzyl-3-(Boc-Amino)Pyrrolidine
  • (R)-1-Benzyl-3-(Tert-Butoxycarbonylamino)Pyrrolidine
  • (R)-(1-Benzyl-Pyrrolidin-3-Yl)-Carbamic Acid Tert-Butyl Ester
  • Tert-Butyl(R)-1-Benzylpyrrolidin-3-Ylcarbamate
  • Carbamic Acid,[(3R)-1-(Phenylmethyl)-3-Pyrrolidinyl]-,1,1-Dimethylethyl Ester
  • Tert-Butyl [(3R)-1-Benzylpyrrolidin-3-Yl]Carbamate
  • Tert-Butyl (1-Benzylpyrrolidin-3-Yl)Carbamate
  • 1-Benzyl-3-(Boc-Amino)Pyrrolidine
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