Reacción #657311

ord-5fdc646e557142ff9c0d88ee8192ca33

Ecuación de reacción

Oc1cc(-c2ccc(F)cc2)n[nH]1
3-(4-fluorophenyl)-1H-pyrazol-5-ol
O=C([O-])[O-].[K+].[K+]
K2CO3
CC(OS(C)(=O)=O)C(C)OS(C)(=O)=O
butane-2,3-diyl dimethanesulfonate
CC1Oc2cc(-c3ccc(F)cc3)nn2C1C
6-(4-fluorophenyl)-2,3-dimethyl-2,3-dihydropyrazolo[5,1-b][1,3]oxazole
Rendimiento 71.8%

Disolventes

Condiciones de reacción

Temperatura
60°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroprepared
  2. 2
    Otroat room temperature
  3. 3
    Extracciónextracted with ethyl acetate
  4. 4
    SecadoThe organic layer was dried over anhydrous sodium sulphate
  5. 5
    Concentraciónconcentrated
  6. 6
    Otroto get the crude product
  7. 7
    OtroPurification by column chromatography over silica gel (eluent 5-10% ethyl acetate in petrol ether)

Procedimiento

To a solution of 3-(4-fluorophenyl)-1H-pyrazol-5-ol (3 g, 16.8 mmol) in DMF (15 mL) was added K2CO3 (9.3 g, 67.4 mmol) and butane-2,3-diyl dimethanesulfonate (4.8 g, 18.5 mmol) (prepared as described in US2010/41748) at room temperature and then stirred for 16 h at 60° C. Thereafter, the reaction mixture was diluted with cold water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulphate and concentrated to get the crude product. Purification by column chromatography over silica gel (eluent 5-10% ethyl acetate in petrol ether) yielded 6-(4-fluorophenyl)-2,3-dimethyl-2,3-dihydropyrazolo[5,1-b][1,3]oxazole (2.8 g, 71%) as yellow oil and a mixture of diastereoisomers.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09023844B2uspto-grants-2015_05