HRID335276

反应详情

EQUATION

反应方程式

HRID 335276 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
70 °C

PROCEDURE

实验过程

4-Fluoro-3-{[7-(2-methyl-2H-pyrazol-3-yl)-imidazo[1,2-a]pyridine-3-carbonyl]-amino}-benzoic acid (step 2) (450 g, 1.19 mol), EDC.HCl (454.8 g, 2.372 mol) and HOBt (181.6 g, 1.186 mol) in DMF (3.2 L) at 25° C. were stirred for 1.5 hr. The reaction was monitored by HPLC. To the reaction mixture was dropwise added cis 2-(2,6-dimethyl-piperidin-1-yl)-ethylamine (222.5 g, 1.423 mol) over 10 min and stirring continued for 30 min. To the reaction mixture was dropwise an aqueous solution of Na2CO3 (5%, 6 L) over 120 min and the resulting solid was collected by filtration and washed with water (5 L). To the solid was added ethanol (5 L) followed by heating to 70° C. to obtain a clear solution. Water (1.5 L) was dropwise added at 70° C. and stirred for 30 min. The clear solution was slowly cooled to 25° C. over 2 hr. The solid was filtered, washed with ethanol (500 mL) and dried under vacuum at 50° C. overnight to afford the title compound as a white solid;

WORKUP

后处理

  1. customover 10 min
  2. customover 120 min
  3. filtrationthe resulting solid was collected by filtration
  4. washwashed with water (5 L)
  5. additionTo the solid was added ethanol (5 L)
  6. customto obtain a clear solution
  7. stirringstirred for 30 min
  8. temperatureThe clear solution was slowly cooled to 25° C. over 2 hr
  9. filtrationThe solid was filtered
  10. washwashed with ethanol (500 mL)
  11. customdried under vacuum at 50° C. overnight