HRID2036191

反应详情

EQUATION

反应方程式

HRID 2036191 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

A mixture of (2-tert-butoxycarbonylamino-2-methyl-propylamino)-acetic acid methyl ester (compound N; 26.5 g) in DCM (800 mL) was stirred at ambient temperature, TFA (180 mL) was added drop-wise. The mixture was stirred at 30-40° C. for 5 h before it was concentrated in vacuo. The residue was partitioned between dissolved toluene and water. The organic layer was dried over Na2SO4, filtered, and concentrated in vacuo. The residual solid was dissolved in a mixture of ethanol (400 mL) and methanol (90 mL). K2CO3 (207 g) was added and the mixture was refluxed overnight. The mixture was cooled to room temperature. DCM (2500 mL) was added, and the mixture was stirred for 1 hour at ambient temperature. The solid was filtered off, and the filtrate was concentrated in vacuo to afford 6,6-dimethyl-piperazin-2-one (Compound I; 5.85 g) as a white solid sufficiently pure for the next step.

WORKUP

后处理

  1. stirringThe mixture was stirred at 30-40° C. for 5 h before it
  2. concentrationwas concentrated in vacuo
  3. customThe residue was partitioned
  4. dissolutionbetween dissolved toluene and water
  5. dry with materialThe organic layer was dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. dissolutionThe residual solid was dissolved in a mixture of ethanol (400 mL) and methanol (90 mL)
  9. additionK2CO3 (207 g) was added
  10. temperaturethe mixture was refluxed overnight
  11. temperatureThe mixture was cooled to room temperature
  12. additionDCM (2500 mL) was added
  13. stirringthe mixture was stirred for 1 hour at ambient temperature
  14. filtrationThe solid was filtered off
  15. concentrationthe filtrate was concentrated in vacuo