Reacción #217175

ord-f3461d38c96545538266498be3b441f1

Reactivos

Ninguno

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Concentraciónconcentrated under reduced pressure
  2. 2
    workup.ADDITIONToluene was added to the residue
  3. 3
    Concentraciónthe solution was again concentrated under reduced pressure
  4. 4
    workup.DISSOLUTIONThe resulting residue was dissolved in ether (5 ml)
  5. 5
    workup.ADDITIONAddition of hexane (ca. 10 ml)
  6. 6
    Otroprecipitation
  7. 7
    FiltraciónFiltration of a precipitate
  8. 8
    Otroby drying in vacuo

Procedimiento

To Boc-Leu-DTrp-βAla-OEt (760 mg) obtained in Example 29-(1) was added 20% ethanedithiol/TFA (25 ml) at 0°~5° C. The reaction mixture was stirred at 0°~5° C. for 30 min, and concentrated under reduced pressure. Toluene was added to the residue and the solution was again concentrated under reduced pressure. These procedures were repeated 3 times. The resulting residue was dissolved in ether (5 ml). Addition of hexane (ca. 10 ml) caused precipitation. Filtration of a precipitate, followed by drying in vacuo gave Leu-DTrp-βAla-OEt.TFA (781 mg) as a pale yellow solid. To the solid (781 mg) was added sat. NaHCO3. Extraction with chloroform, followed by drying the organic layer over MgSO4, and concentration of the resulting solution under reduced pressure, gave the product (479 mg).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05470833uspto-grants-1995_11