Reacción #318032

ord-40ed8f21b3f240d0ba363c9f08270111

Ecuación de reacción

Cn1cc(Br)c(-c2cccc(N)c2)n1
3-(4-bromo-1-methyl-1H-pyrazol-3-yl)aniline
O=C([O-])[O-].[Na+].[Na+]
sodium carbonate
Cn1ccc(-c2cccc(N)c2)n1
title compound
Rendimiento 72.8%
Cn1ccc(-c2cccc(N)c2)n1
3-(1-Methyl-1H-pyrazol-3-yl)aniline
Rendimiento 72.8%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe mixture was filtered through ‘hyflo’
  2. 2
    Filtraciónfilter aid
  3. 3
    Lavadothe filter pad washed with ethanol (50 ml)
  4. 4
    OtroThe combined filtrate was evaporated in vacuo
  5. 5
    Otroto give a brown gum
  6. 6
    Extracciónextracted with ethyl acetate (2×100 ml)
  7. 7
    Secadothe organic layer was dried over magnesium sulphate
  8. 8
    Otrothe solvent removed in vacuo
  9. 9
    OtroPurification by chromatography on silica gel
  10. 10
    Lavadoeluting with diethyl ether

Procedimiento

A solution of 3-(4-bromo-1-methyl-1H-pyrazol-3-yl)aniline (1.0 g) (available from Maybridge) in ethanol (20 ml) was added to a pre-hydrogenated suspension of 5% palladium on charcoal (0.5 g) in ethanol (40 ml). The resulting suspension was stirred under an atmosphere of hydrogen for 3 h. The mixture was filtered through ‘hyflo’ filter aid and the filter pad washed with ethanol (50 ml). The combined filtrate was evaporated in vacuo to give a brown gum. This gum was treated with 2M sodium carbonate solution (100 ml) and extracted with ethyl acetate (2×100 ml); the organic layer was dried over magnesium sulphate and the solvent removed in vacuo. Purification by chromatography on silica gel, eluting with diethyl ether, gave the title compound as a white crystalline solid (0.5 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07566786B2uspto-grants-2009_07