HRID521215

反应详情

EQUATION

反应方程式

HRID 521215 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
95 °C

PROCEDURE

实验过程

To a microwave vial was added tert-butyl 4-(3-amino-4-carbamoyl-1H-pyrazol-1-yl)-4-(cyanomethyl)piperidine-1-carboxylate (Intermediate 35-1) (5.0 g, 14 mmol), 4-bromo-2-fluoropyridine (2.5 g, 14 mmol), K3PO4 (6.1 g, 29 mmol), and dioxane (72 mL). The mixture was degassed with bubbling argon for 5 minutes. Pd2(dba)3 (0.7 g, 0.7 mmol) and X-Phos (1.0 g, 2.2 mmol) were then added, and the vial was sealed and heated to 95° C. for 5 hours. The mixture was then cooled to ambient temperature, diluted with EtOAc, filtered through celite, and eluted with EtOAc. The filtrate was concentrated in vacuo, and the resulting yellow oil was purified by MPLC on silica gel (using a gradient elution of 50-100% EtOAc/hexanes) to afford the title compound, Example #9-1.

WORKUP

后处理

  1. customThe mixture was degassed with bubbling argon for 5 minutes
  2. customthe vial was sealed
  3. temperatureThe mixture was then cooled to ambient temperature
  4. filtrationfiltered through celite
  5. washeluted with EtOAc
  6. concentrationThe filtrate was concentrated in vacuo
  7. customthe resulting yellow oil was purified by MPLC on silica gel (
  8. washa gradient elution of 50-100% EtOAc/hexanes)