Reacción #75899

ord-5a38d8ca83fe481f95fcda3c99627090

Ecuación de reacción

O
Water
CCn1nc(C)c(C(=O)c2ccccc2)c1Cl
(5-chloro-1-ethyl-3-methyl-1H-pyrazol-4-yl)-phenyl-methanone
COc1ccc(O)cc1
4-methoxyphenol
[H-].[Na+]
sodium hydride
CCn1nc(C)c(C(=O)c2ccccc2)c1Oc1ccc(OC)cc1
[1-ethyl-5-(4-methoxyphenoxy)-3-methyl-1H-pyrazol-4-yl]-phenyl-methanone
Rendimiento 57.3%

Condiciones de reacción

Temperatura
110°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónthe mixture was extracted three times with 10 ml of dichloromethane
  2. 2
    SecadoThe combined extracts were dried over magnesium sulphate
  3. 3
    Filtraciónfiltered
  4. 4
    Otroevaporated
  5. 5
    OtroThe residue was purified by flash chromatography on silica gel
  6. 6
    Lavadofor the elution

Procedimiento

A mixture of 129 mg of (5-chloro-1-ethyl-3-methyl-1H-pyrazol-4-yl)-phenyl-methanone, 141 mg of 4-methoxyphenol and 33 mg of sodium hydride (60% in mineral oil) in 3 ml of anhydrous N,N-dimethylformamide was stirred under nitrogen at 110° C. for 5 h. Water (8 ml) was added and the mixture was extracted three times with 10 ml of dichloromethane. The combined extracts were dried over magnesium sulphate, filtered and evaporated. The residue was purified by flash chromatography on silica gel using ethyl acetate/petroleum ether (bp 40-60° C.) (1:3) for the elution to give 100 mg of [1-ethyl-5-(4-methoxyphenoxy)-3-methyl-1H-pyrazol-4-yl]-phenyl-methanone as a yellow oil. Mass spectrum (ES) m/z 337 [M]+, 378 [M+H+CH3CN]+.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US06699887B2uspto-grants-2004_03