Reacción #83660

ord-ec1f91f9d22b4f8780dfa3a44b4287d7

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe solvents were evaporated under reduced pressure
  2. 2
    workup.DISSOLUTIONthe residue was dissolved in water/acetonitrile
  3. 3
    OtroThe crude product was purified by HPLC (C-18 DeltaPak column)
  4. 4
    OtroBoth diastereomers were separated

Procedimiento

A portion of ethyl β-[[2(R)-[[[[4-(aminoiminomethyl)phenyl]amino]carbonyl]-amino]methylpropanoyl]amino]-1,3-benzodioxole-5-propanoate (0.18 g; 0.37 mmoles)) was then treated with 1N lithium hydroxide in methanol/water (1:1; 10 ml) for 15 min. The solvents were evaporated under reduced pressure and the residue was dissolved in water/acetonitrile. The crude product was purified by HPLC (C-18 DeltaPak column) using a gradient of acetonitrile/water/trifluoroacetic acid. Both diastereomers were separated and the desired fractions were lyophilized to give 121 mg of white solid (71% combined yield). FAB-MS: MH+ =456.3 (isomer 1) and 456.2 (isomer 2).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05624956uspto-grants-1997_04