Reacción #495359

ord-06dc2515088a4d57ba10101cb25a684f

Condiciones de reacción

Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGthe reaction was stirred at room temperature for 2 hours
  2. 2
    workup.STIRRINGstirred for 10 minutes
  3. 3
    OtroThe solid formed
  4. 4
    Filtraciónwas collected by filtration
  5. 5
    Lavadowashed with ether
  6. 6
    Otrodried

Procedimiento

NaH (0.960 g, 24.0 mmol, 60% dispersion in mineral oil) at 0° C. was added to 4-chloro-5-iodo-1H-pyrrolo[2,3-b]pyridine (5.57 g, 20.0 mmol) in dimethylformamide (“DMF”; 40 mL) and stirred at 0° C. for 20 minutes. Benzenesulfonyl chloride (2.82 mL, 22.0 mmol) was added, and the reaction was stirred at room temperature for 2 hours. Water (200 mL) was added and stirred for 10 minutes. The solid formed was collected by filtration, washed with ether, and dried to give 4-chloro-5-iodo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine (8.20 g, 98% yield).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08758830B2uspto-grants-2014_06