HRID16798

反应详情

EQUATION

反应方程式

HRID 16798 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

Methyl 4-(1-cyclopropylpiperidin-4-yl)benzoate (0.259 g, 1 mmol), 5-[2-(3,5-dimethoxyphenyl)ethyl]-2H-pyrazol-3-amine (0.247 g, 1.00 mmol) in toluene (10 ml) was treated with a 2M solution of trimethylaluminium (1.250 ml, 2.50 mmol) in toluene,under nitrogen. The reaction mixture was heated at 60° C. for 18 h. The reaction mixture was cooled and the reaction quenched with methanol (40 ml) and acidified with 2N HCl (1 ml). The crude reaction mixture was purified by ion exchange chromatography, using an SCX column. The crude product was eluted from the column using 7M NH3/MeOH and fractions were evaporated to dryness. The crude product was purified by silica column chromatography, eluting with a gradient of 0 to 5% 2.5M ammonia/methanol in DCM. Pure fractions were evaporated to dryness and the product crystallised from DCM/diethyl ether to give the title compound (0.170 g, 35.8%) as a white solid.

WORKUP

后处理

  1. temperatureThe reaction mixture was cooled
  2. customthe reaction quenched with methanol (40 ml)
  3. customThe crude reaction mixture
  4. customwas purified by ion exchange chromatography
  5. washThe crude product was eluted from the column
  6. customwere evaporated to dryness
  7. customThe crude product was purified by silica column chromatography
  8. washeluting with a gradient of 0 to 5% 2.5M ammonia/methanol in DCM
  9. customPure fractions were evaporated to dryness
  10. customthe product crystallised from DCM/diethyl ether