反应 #215578

ord-0ca0f74614af45378ca5b5ef88cf8ed7

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas added dropwise over the period of 5 minutes
  2. 2
    workup.STIRRINGThe mixture was then stirred at 30° C. for 30 minutes
  3. 3
    其他After the reaction
  4. 4
    温度the reactor was cooled with ice
  5. 5
    萃取The solution was then extracted with 100 ml of toluene
  6. 6
    洗涤The toluene layer was washed with 50 ml of a saturated aqueous solution of sodium chloride and 50 ml of water
  7. 7
    其他the solvent was removed by concentration under reduced pressure
  8. 8
    其他to afford a yellowish white solid
  9. 9
    其他Recrystallization of the solid from ethanol

实验过程

2,3-Dicyano-5-chloro-6-phenylpyrazine (2.41 g; 0.01 mole) was dissolved in 30 ml of tetrahydrofuran, and with stirring at 15° to 20° C., a solution prepared from 2.04 g (0.02 mole) of DL-α-amino-n-butyric acid, 1.12 g (0.02 mole) of potassium hydroxide and 40 ml of water was added dropwise over the period of 5 minutes. The mixture was then stirred at 30° C. for 30 minutes. After the reaction, the reactor was cooled with ice, and in the meanwhile, 2 ml of conc. hydrochloric acid was added to the reaction solution. The solution was then extracted with 100 ml of toluene. The toluene layer was washed with 50 ml of a saturated aqueous solution of sodium chloride and 50 ml of water, and the solvent was removed by concentration under reduced pressure to afford a yellowish white solid. Recrystallization of the solid from ethanol afforded 2.63 g (yield 86%) of 2,3-dicyano-5-(1-carboxy-n-propyl)amino-6-phenylpyrazine.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US04259489uspto-grants-1981_03