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CAS 142253-50-7

:

(S)-tert-Butyl 2-(cyanomethyl)pyrrolidine-1-carboxylate

Description:
(S)-tert-Butyl 2-(cyanomethyl)pyrrolidine-1-carboxylate is a chiral compound characterized by its pyrrolidine ring structure, which is a five-membered nitrogen-containing heterocycle. The presence of the tert-butyl group enhances its lipophilicity, making it more soluble in organic solvents. The cyanomethyl group introduces a nitrile functional group, which can participate in various chemical reactions, including nucleophilic additions and cycloadditions. This compound is typically used in organic synthesis, particularly in the preparation of more complex molecules due to its ability to serve as a building block. Its chirality, indicated by the (S) configuration, is significant in pharmaceutical applications, as it can influence the biological activity and interaction with biological targets. The carboxylate moiety contributes to its reactivity, allowing for potential derivatization. Overall, this compound is of interest in medicinal chemistry and synthetic organic chemistry due to its unique structural features and functional groups.
Formula:C11H18N2O2
InChI:InChI=1/C11H18N2O2/c1-11(2,3)15-10(14)13-8-4-5-9(13)6-7-12/h9H,4-6,8H2,1-3H3
SMILES:CC(C)(C)OC(=O)N1CCCC1CC#N
Synonyms:
  • 1-pyrrolidinecarboxylic acid, 2-(cyanomethyl)-, 1,1-dimethylethyl ester, (2S)-
  • tert-butyl (2S)-2-(cyanomethyl)pyrrolidine-1-carboxylate
  • Tert-Butyl 2-(Cyanomethyl)Pyrrolidine-1-Carboxylate
  • 2-(cyanomethyl)-1-pyrrolidinecarboxylic acid tert-butyl ester
  • (S)-TERT-BUTYL 2-(CYANOMETHYL)PYRROLIDINE-1-CARBOXYLATE
  • (S)-1-Boc-2-(cyanomethyl)pyrrolidine
  • N-BOC-(2S)-PYRR(2-CHCN)
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