Reacción #1483067

ord-46a8c47f49664915a044db974d078b71

Ecuación de reacción

COC(=O)c1ccc2cc[nH]c2c1
1H-indole-6-carboxylic acid methyl ester
FC(F)Oc1ccc(CBr)cc1
4-difluoromethoxy-benzyl bromide
[H-].[Na+]
sodium hydride
COC(=O)c1ccc2ccn(Cc3ccc(OC(F)F)cc3)c2c1
1-(4-difluoromethoxy-phenylmethyl)-1H-indole-6-carboxylic acid methyl ester
Rendimiento 21.1%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Lavadothe organic layer was washed again with dilute NaHCO3 (25 mL)
  2. 2
    SecadoThe organic layer was dried over Na2SO4
  3. 3
    Filtraciónfiltered
  4. 4
    Concentraciónconcentrated

Procedimiento

To a solution of commercially available 1H-indole-6-carboxylic acid methyl ester (0.35 g, 2.0 mmol) and 4-difluoromethoxy-benzyl bromide (0.52 g, 2.2 mmol) in DMF (2 mL) was added sodium hydride (92 mg, 2.3 mmol). After stirring at room temperature for 3.5 hr, the solution was diluted with water (25 mL) and ethyl acetate (75 mL), the organic layer was washed again with dilute NaHCO3 (25 mL) and then brine (25 mL). The organic layer was dried over Na2SO4, filtered and concentrated. The remaining residue was subjected to flash chromatography (ethyl acetate/hexane. 1:5) to provide 1-(4-difluoromethoxy-phenylmethyl)-1H-indole-6-carboxylic acid methyl ester as a colorless oil (0.14 g, 21% yield).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08900565B2uspto-grants-2014_12