HRID539753

反应详情

EQUATION

反应方程式

HRID 539753 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
215 °C

PROCEDURE

实验过程

An 8 mL vial is charged with N-[5-(6-chloroimidazo[2,1-f]pyridazin-2-yl)-2-(trifluoromethyl)phenyl]-2,2-dimethyl-propanamide (0.059 g, 0.15 mmol), copper cyanide (0.035 g, 0.3 mmol), and 4-methylmorpholine (0.43 mL). The mixture is stirred at 215° C. for 4 hr in the microwave, then cooled, diluted with Et2O, sat. aqueous NaHCO3 and the biphasic mixture is filtered. Organics are collected and aqueous layer is extracted twice more with Et2O. Organics are combined, dried, concentrated, and purified by prep plate TLC (1:1 Hex:EtOAc) to give the title compound (15 mg, 26% yield). LCMS m/z=388.5 [M+H]+, tR=2.56 min. (compound same as Example 173)

WORKUP

后处理

  1. temperaturecooled
  2. filtrationthe biphasic mixture is filtered
  3. customOrganics are collected
  4. extractionaqueous layer is extracted twice more with Et2O
  5. customdried
  6. concentrationconcentrated
  7. custompurified by prep plate TLC (1:1 Hex:EtOAc)