Реакция #2186239

ord-b1f7c3f03daf49ad86ee986791df6975

Уравнение реакции

Cc1n[nH]c(=O)c(-c2c(F)cc(F)cc2F)c1-c1ccc(F)cc1
5-(4-fluorophenyl)-6-methyl-4-(2,4,6-trifluorophenyl)-2H-pyridazin-3-one
O=P(Cl)(Cl)Cl
phosphorus oxychloride
Cc1nnc(Cl)c(-c2c(F)cc(F)cc2F)c1-c1ccc(F)cc1
3-chloro-5-(4-fluorophenyl)-6-methyl-4-(2,4,6-trifluorophenyl)pyridazine
Выход 94.0%

Условия реакции

Температура
110°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Температураto cool down to room temperature
  2. 2
    Концентрированиеconcentrated under reduced pressure
  3. 3
    workup.ADDITIONTo the residue was added ethyl acetate and ice water
  4. 4
    Другоеwas separated to two layer
  5. 5
    ПромывкаThe organic layer was washed sequentially with water and saturated brine
  6. 6
    Сушкаdried over anhydrous sodium sulfate
  7. 7
    Концентрированиеconcentrated under reduced pressure

Методика

2.36 g of 5-(4-fluorophenyl)-6-methyl-4-(2,4,6-trifluorophenyl)-2H-pyridazin-3-one and 10 g of phosphorus oxychloride were mixed and stirred at 110° C. for 1 hour. The reaction mixture was allowed to cool down to room temperature and concentrated under reduced pressure. To the residue was added ethyl acetate and ice water, and was separated to two layer. The organic layer was washed sequentially with water and saturated brine, and dried over anhydrous sodium sulfate, then, concentrated under reduced pressure, to obtain 2.34 g of 3-chloro-5-(4-fluorophenyl)-6-methyl-4-(2,4,6-trifluorophenyl)pyridazine (hereinafter, referred to as compound (xviii) of the present invention).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07569518B2uspto-grants-2009_08