Reacción #2186223

ord-ed6374a914874b30bd34fbdf0dca232b

Condiciones de reacción

Temperatura
135°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted with ethyl acetate
  2. 2
    SecadoThe organic phase was dried over magnesium sulfate
  3. 3
    Otroevaporated to dryness
  4. 4
    Otropurified by flash chomatography (silica, chloroform/ethanol) with subsequently trituration with tetrachloromethane

Procedimiento

A stirred mixture of 5-amino-1 -(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulfinyl-1 H-pyrazole-3-carbonitrile (5.00 g, 11.4 mmol) and sulfuric acid (50%, 100 ml) was heated to 135° C. for 3 hours. The cooled mixture was added to ice water and the pH adjusted to 4 by the addition of aqueous sodium hydroxide (6 N, approx. 230 ml), and then extracted with ethyl acetate. The organic phase was dried over magnesium sulfate, evaporated to dryness and purified by flash chomatography (silica, chloroform/ethanol) with subsequently trituration with tetrachloromethane to give the title compound (3.00 g, yield 77%) as off-white crystals, mp 213° C., 1H NMR (DMSO-d6): 5.69 (bs, 2H, NH2), 5.76 (s, 1H, pyrazole-H), and 8.20 (s, 2H, Ar—H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07569516B2uspto-grants-2009_08