Reaktion #51751

ord-be050adf2f374660821e0dfc54325ed2

Lösungsmittel

Reaktionsbedingungen

Temperatur
-40°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    workup.STIRRINGthe solution was stirred at −35° C. for 30 minutes
  3. 3
    TemperaturThe reaction mixture was slowly warmed to room temperature
  4. 4
    Sonstigewas quenched with saturated NH4Cl solution
  5. 5
    workup.ADDITIONEtOAc (200 mL) was added
  6. 6
    Waschenthe organic layer was washed with brine
  7. 7
    Trocknendried (MgSO4)
  8. 8
    Einengenconcentrated
  9. 9
    workup.DISSOLUTIONThe residue was dissolved in 100 mL of THF
  10. 10
    workup.STIRRING2 mL of concentrated HCl and stirred at room temperature for 1 hour
  11. 11
    workup.ADDITIONThe solution was diluted with EtOAc
  12. 12
    Waschenwashed with NaHCO3 solution and brine
  13. 13
    Trocknendried (MgSO4)
  14. 14
    SonstigeThe crude product was purified by flash silica gel chromatography

Vorschrift

(5-tert-Butyl-4-mercapto-2-methyl-phenyl)-carbamic acid tert-butyl ester (prepared in Example EE; 20 g, 68 mmol) was dissolved in 100 mL of THF, cooled to −40° C., and treated dropwise with sec-butyllithium (1.3 M, 156 mL, 203 mmol). After the addition was complete, the reaction mixture was stirred at −30° C. to −45° C. for 30 minutes. To the mixture was added DMF (14.8 g, 203.39 mmol), and the solution was stirred at −35° C. for 30 minutes. The reaction mixture was slowly warmed to room temperature and was quenched with saturated NH4Cl solution. EtOAc (200 mL) was added; the organic layer was washed with brine, dried (MgSO4) and concentrated. The residue was dissolved in 100 mL of THF and 2 mL of concentrated HCl and stirred at room temperature for 1 hour. The solution was diluted with EtOAc, washed with NaHCO3 solution and brine, and dried (MgSO4). The crude product was purified by flash silica gel chromatography to give the title compound. MS(APCI): 304 (M−H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06852711B2uspto-grants-2005_02