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CAS 99735-30-5

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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 ring, which is a five-membered nitrogen-containing heterocycle. The presence of a benzyl group enhances its lipophilicity, making it more soluble in organic solvents. The tert-butoxycarbonyl (Boc) group serves as a protecting group for the amino functionality, which is crucial in synthetic organic chemistry for the selective modification of amino acids and peptides. This compound is typically used in the synthesis of pharmaceuticals and biologically active molecules due to its ability to participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Its chirality, indicated by the (3R) configuration, is significant for biological activity, as enantiomers can exhibit different pharmacological effects. The compound's stability and reactivity can be influenced by the steric and electronic properties of the substituents, making it a valuable intermediate in medicinal chemistry. Overall, (3R)-(+)-1-Benzyl-3-(Tert-Butoxycarbonylamino)Pyrrolidine is an important building block in the development of complex organic compounds.
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)
SMILES:CC(C)(C)OC(=NC1CCN(Cc2ccccc2)C1)O
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
  • N-[1-(phenylmethyl)-3-pyrrolidinyl]carbamic acid tert-butyl ester
  • See more synonyms
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