Reacción #8717

ord-b0655c26605e4b4cb0926cd201146d73

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawhile cooling with ice
  2. 2
    workup.ADDITIONpoured onto ice water
  3. 3
    LavadoThe organic phase is washed with water
  4. 4
    Secadodried over magnesium sulfate
  5. 5
    Otrothe solvent is removed in vacuo

Procedimiento

1.64 g (5.25 mmol) of 2-(2-ethoxyphenyl)-6-methyl-8-propyl-3H-imidazo[1,5-a][1,3,5]triazin-4-one (example VI) are added in portions to 3.14 ml of chlorosulfonic acid while cooling with ice. The reaction mixture is stirred at room temperature for 16 hours, then diluted with dichloromethane and poured onto ice water. The organic phase is washed with water and dried over magnesium sulfate and the solvent is removed in vacuo. 2.15 g (99%) of 4-ethoxy-3-(6-methyl-4-oxo-8-propyl-3,4-dihydro-imidazo[1,5-a][1,3,5]triazin-2-yl)-benzene-sulfonyl chloride are obtained.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091203B2uspto-grants-2006_08