Реакция #73460

ord-db8e1d54094c4a8cb96526c15bfc728f

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGthe mixture was stirred at 70° C. for 2 h
  2. 2
    ТемператураAfter cooling down to room temperature
  3. 3
    Фильтрацияfiltered over celite
  4. 4
    ПромывкаThe filter cake was washed thoroughly
  5. 5
    Другоеthe organic layer was evaporated

Методика

7-Chloro-6-fluoro-2H-isoquinolin-1-one (prepared according to WO 2007/012422; 52.2 g) was dissolved in THF (1 L). After addition of silver carbonate (145.5 g) and benzyl bromide (40.6 mL), the mixture was stirred at room temperature overnight. Another 6.2 mL of benzyl bromide were added and the mixture was stirred at 70° C. for 2 h. After cooling down to room temperature, the reaction mixture was diluted by addition of 1 L of ethyl acetate and filtered over celite. The filter cake was washed thoroughly, the organic layer was evaporated and subjected to silica gel chromatography (n-heptanes: methyl tert. butyl ether) to give 27.8 g of the title compound (38). Rt=3.73 min (Method 1). Detected mass: 288.1 (M+H+).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08541449B2uspto-grants-2013_09