Reaktion #1983

ord-3c14aa7c3cf94af8afc09046f03b475b

Reaktionsgleichung

O=C(O)C1(C(F)(F)F)CCN(Cc2ccccc2)C1
compound
O=C(O)C1(C(F)(F)F)CCN(Cc2ccccc2)C1
1-benzyl-3-trifluoromethylpyrrolidine-3-carboxylic acid
[N-]=[N+]=NP(=O)(c1ccccc1)c1ccccc1
diphenylphosphoryl azide
CN(C)C
trimethyl amine
CC(C)(C)O
t-butanol
CC(C)(C)OC(=O)NC1(C(F)(F)F)CCN(Cc2ccccc2)C1
title compound
Ausbeute 96.7%
CC(C)(C)OC(=O)NC1(C(F)(F)F)CCN(Cc2ccccc2)C1
1-benzyl-3-(BOC-amino)-3-trifluoromethylpyrrolidine
Ausbeute 96.7%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturwas heated
  2. 2
    Temperaturat reflux under N2 for 24 hours
  3. 3
    EinengenThe mixture was concentrated to dryness
  4. 4
    workup.DISSOLUTIONthe residue was dissolved in methylene chloride
  5. 5
    WaschenThe solution was washed with satd
  6. 6
    EinengenNaHCO3 and water, then concentrated
  7. 7
    SonstigeThe residue was chromatographed on silica gel

Vorschrift

A mixture of 1.42 g of the compound from step 454a, 1.71 g of diphenylphosphoryl azide, 12.3 g of t-butanol and 0.627 g of trimethyl amine was heated at reflux under N2 for 24 hours. The mixture was concentrated to dryness, and the residue was dissolved in methylene chloride. The solution was washed with satd. NaHCO3 and water, then concentrated. The residue was chromatographed on silica gel to give 1.73 g of the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726182uspto-grants-1998_03