HRID1410413

反应详情

EQUATION

反应方程式

HRID 1410413 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
12.5 °C

PROCEDURE

实验过程

A vessel at room temperature was charged with formic acid (800 mL) and 4-methyl-2-(3-(1-methylpiperidin-4-yl)propylamino)pyrimidine-5-carbonitrile (100 g) and the resulting mixture stirred to yield a clear solution, then cooled to 10-15° C. Water (200 mL) was added and the resulting mixture cooled to −2 to 0° C. To the resulting mixture was then added RANEY® nickel (160 g) maintaining the temperature at −2 to 0° C. and then stirred at this temperature for 2-3 hours. The resulting mixture was then filtered to remove the RANEY® nickel and the filtercake washed with water (100 mL), The filtrate was cooled to 0-5° C. and then slowly treated with 50% sodium carbonate solution in water (3.0 L) to adjust the pH of the solution to pH˜10. Toluene (400 mL) was added and the resulting mixture stirred at room temperature for about 30 minutes, then allowed to settle for about 1 hour. The resulting layers were separated and the aqueous layer washed with toluene (400 mL×2). The combined toluene layer and washed were distilled at 55-60° C. to remove the toluene, to yield the title compound as an oily residue.

WORKUP

后处理

  1. customto yield a clear solution
  2. temperaturethe resulting mixture cooled to −2 to 0° C
  3. stirringstirred at this temperature for 2-3 hours
  4. filtrationThe resulting mixture was then filtered
  5. customto remove the RANEY® nickel
  6. washthe filtercake washed with water (100 mL)
  7. temperatureThe filtrate was cooled to 0-5° C.
  8. additionslowly treated with 50% sodium carbonate solution in water (3.0 L)
  9. additionToluene (400 mL) was added
  10. stirringthe resulting mixture stirred at room temperature for about 30 minutes
  11. customThe resulting layers were separated
  12. washthe aqueous layer washed with toluene (400 mL×2)
  13. washThe combined toluene layer and washed
  14. distillationwere distilled at 55-60° C.
  15. customto remove the toluene