Reacción #2188937

ord-77f23bbb2da6434fa66d8b4ca29d65cb

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONAfter addition
  2. 2
    Otrothe ice bath was removed
  3. 3
    TemperaturaThe mixture was cooled in an ice bath
  4. 4
    Otroquenched
  5. 5
    workup.ADDITIONby adding saturated sodium bicarbonate until the mixture
  6. 6
    workup.ADDITIONMore DCM (400 mL) was added
  7. 7
    Otrothe organic layer was separated
  8. 8
    Lavadowashed with brine
  9. 9
    Otrodried
  10. 10
    Concentraciónconcentrated under vacuum
  11. 11
    workup.DISSOLUTIONThe crude product (6.5 g) was dissolved in 50 mL of hot MeOH
  12. 12
    TemperaturaAfter cooling
  13. 13
    Filtraciónthe crystallized product was collected by filtration
  14. 14
    Lavadowashed once with MeOH

Procedimiento

Boron trichloride methyl sulfide complex (51 mL, 2.0 M solution in DCM) was added to 6.4 (8.2 g, 17 mmol) in DCM (100 mL) at 0° C. After addition, the ice bath was removed, and the mixture was stirred at room temperature for 7 hours. The mixture was cooled in an ice bath and quenched by adding saturated sodium bicarbonate until the mixture was neutralized. More DCM (400 mL) was added, and the organic layer was separated, washed with brine, dried, and concentrated under vacuum. The crude product (6.5 g) was dissolved in 50 mL of hot MeOH. After cooling, the crystallized product was collected by filtration and washed once with MeOH to give 6.5 (4.2 g). The filtrate was concentrated, and the solid that formed was collected and washed to give an additional 1.2 g of compound 6.5. MS ESI (pos.) m/e: 393 (M+H). 1H NMR (CDCl3) δ 8.29(d, 1H), 7.30 (m, 3H), 7.20 (d, 2H), 7.15 (d, 2H), 6.95 (d, 2H), 6.14 (d, 1H), 4.71 (dd, 1H), 4.63 (m, 1H), 4.16 (d, 2H), 4.00 (dd, 1H), 3.54 (dd, 1H), 3.21 (dd, 1H), 2.76 (dd, 1H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07572934B2uspto-grants-2009_08