Reacción #1076986

ord-e8ea92b8528041f484958dbcbab02358

Condiciones de reacción

Temperatura
35°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas treated with the reaction mixture from above,
  2. 2
    Temperaturato reflux
  3. 3
    workup.ADDITIONUpon complete addition
  4. 4
    workup.STIRRINGthe resulting crystalline slurry was stirred at 25° C
  5. 5
    workup.WAITAfter one hour
  6. 6
    Filtraciónthe crystalline product was filtered
  7. 7
    Lavadowashed with cold ethanol (10 mL)
  8. 8
    Otrodried at 40° C. in vacuo

Procedimiento

A solution of 6-methoxy-2-(4-methoxyphenyl)-3-[4-(2-piperidinoethoxy)benzoyl]benzo[b]thiophene hydrochloride (2.0 g) in 1,2-dichloroethane (20 mL) was treated with boron trichloride (2.0 mL). The resulting mixture was stirred at 35° C. for about 18 hours. A mixture of ethanol and methanol (10 mL, 95:5, 3A) was treated with the reaction mixture from above, causing the alcoholic mixture to reflux. Upon complete addition, the resulting crystalline slurry was stirred at 25° C. After one hour, the crystalline product was filtered, washed with cold ethanol (10 mL), and dried at 40° C. in vacuo to give 1.78 g of the title compound. The X-ray powder diffraction pattern is identical to that reported in Table 1.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06458811B1uspto-grants-2002_10