HRID1969834

反应详情

EQUATION

反应方程式

HRID 1969834 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

N,N-Dibenzyl-3-methyl-4-(3-tosyl-3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)cyclopentan-amine (4.47 g, 7.58 mmol) was dissolved in 1,4-dioxane (40 mL). NaOH (2 N aqueous, 4 mL) was added and the reaction mixture was heated at about 90° C. for about 80 min. The organic solvent was removed under reduced pressure and the residue was treated with saturated aqueous NH4Cl (70 mL) and extracted with DCM (2×60 mL). The combined organic extracts were washed with brine (70 mL), dried over anhydrous MgSO4 and concd under reduced pressure. The residue was purified by silica gel chromatography eluting with a gradient of 0-8% MeOH in DCM to yield N,N-dibenzyl-3-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-4-methylcyclopentan-amine (1.84 g, 56%) as a yellow oil: LC/MS (Table 1, Method a) Rt=2.31 min; MS m/z 436 (M+H)+.

WORKUP

后处理

  1. customThe organic solvent was removed under reduced pressure
  2. additionthe residue was treated with saturated aqueous NH4Cl (70 mL)
  3. extractionextracted with DCM (2×60 mL)
  4. washThe combined organic extracts were washed with brine (70 mL)
  5. dry with materialdried over anhydrous MgSO4 and concd under reduced pressure
  6. customThe residue was purified by silica gel chromatography
  7. washeluting with a gradient of 0-8% MeOH in DCM