Reacción #67438

ord-530dd23ccee5450fb2d116346c40c697

Disolventes

Condiciones de reacción

Temperatura
25°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otrothe reaction was quenched with H2O (10 mL)
  2. 2
    workup.ADDITIONThe reaction mixture was diluted with dichloromethane (25 mL)
  3. 3
    Extracciónwas extracted with 1N HCl (30 mL×3) and brine (30 mL)
  4. 4
    SecadoThe organic extracts were dried over Na2SO4
  5. 5
    Otroevaporated
  6. 6
    OtroThe crude product was purified by chromatography on silica gel (eluting with 0-100% ethyl acetate in hexanes)

Procedimiento

Methyl 4-(1-(benzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-2-bromobenzoate (4.12 g, 9.9 mmol) was added to a solution of LiBH4 (429 mg, 19.8 mmol) in THF/ether/H2O (20/20/1 mL) and was allowed to stir at 25° C. After 16 hours, the reaction was quenched with H2O (10 mL). The reaction mixture was diluted with dichloromethane (25 mL) and was extracted with 1N HCl (30 mL×3) and brine (30 mL). The organic extracts were dried over Na2SO4 and evaporated. The crude product was purified by chromatography on silica gel (eluting with 0-100% ethyl acetate in hexanes) to afford 1-(benzo[d][1,3]dioxol-5-yl)-N-(3-bromo-4-(hydroxymethyl)phenyl)cyclopropanecarboxamide (2.84 g, 74%). ESI-MS m/z calc. 389.0, found 390.1 (M+1)+; retention time 2.91 minutes.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08524767B2uspto-grants-2013_09