Reaktion #8226

ord-fcc97bd77b3c4880aa5eed15a29d7d18

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe mixture is filtered
  2. 2
    Sonstigeto remove the Pd/C
  3. 3
    Sonstigethe filtrate is evaporated
  4. 4
    Sonstigeto give a crude oil
  5. 5
    workup.STIRRINGthe mixture is stirred for 5 minutes at this temperature
  6. 6
    Sonstigebefore removing the ice bath
  7. 7
    workup.STIRRINGThe reaction mixture is stirred overnight
  8. 8
    Sonstigebefore being quenched by addition of IN HCl and ethyl acetate
  9. 9
    ExtraktionThe aqueous layer is extracted with ethyl acetate several times
  10. 10
    Waschenthe combined organic extracts are washed twice with brine
  11. 11
    Trocknendried over Na2SO4
  12. 12
    Sonstigeto give a crude oil
  13. 13
    SonstigeThe crude material is purified by flash chromatography (25% ethyl acetate/hexanes)

Vorschrift

3-(2-Nitro-2-methylpropyl)-7-nitroindole (1.89 g, 7.2 mmol) is dissolved in ethyl acetate (75 mL) and 10% Pd/C is added (750 mg). The mixture is stirred under a balloon of nitrogen for 2–3 hours. The mixture is filtered to remove the Pd/C, and the filtrate is evaporated to give a crude oil. This crude 3-(2-nitro-2-methylpropyl)-7-aminoindole is immediately dissolved in pyridine (100 mL) and the solution is cooled with an ice bath to 0° C. Benzenesulfonyl chloride is added slowly, and the mixture is stirred for 5 minutes at this temperature before removing the ice bath. The reaction mixture is stirred overnight before being quenched by addition of IN HCl and ethyl acetate. The aqueous layer is extracted with ethyl acetate several times and the combined organic extracts are washed twice with brine and dried over Na2SO4 to give a crude oil. The crude material is purified by flash chromatography (25% ethyl acetate/hexanes) to provide 1.9 g of 3-(2-nitro-2-methylpropyl)-7-benzenesulfonamidyl-indole (71%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087635B2uspto-grants-2006_08