HRID1854458

反应详情

EQUATION

反应方程式

HRID 1854458 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

To a solution of benzyl 4-methyl-3-(3-tosyl-3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)piperidine-1-carboxylate (0.93 g, 1.7 mmol) in 1,4-dioxane (20 mL) was added aqueous NaOH (2 N, 1.0 mL), and the resulting mixture was heated at about 90° C. for about 80 min. The solvents were removed under reduced pressure and the residue was treated with saturated aqueous NH4Cl (26 mL) and extracted with EtOAc (2×30 mL). The combined organic extracts were washed with brine (20 mL), dried over anhydrous MgSO4, filtered, and concentrated to yield the crude product as a brown amorphous solid. The material was purified by silica gel chromatography eluting with a gradient of 5-100% MeOH/DCM to give benzyl 3-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-4-methylpiperidine-1-carboxylate (0.55 g, 83%) as a yellow solid: LC/MS (Table 2, Method a) Rt=1.94 min; MS m/z: 390 (M+H)+.

WORKUP

后处理

  1. customThe solvents were removed under reduced pressure
  2. additionthe residue was treated with saturated aqueous NH4Cl (26 mL)
  3. extractionextracted with EtOAc (2×30 mL)
  4. washThe combined organic extracts were washed with brine (20 mL)
  5. dry with materialdried over anhydrous MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto yield the crude product as a brown amorphous solid
  9. customThe material was purified by silica gel chromatography
  10. washeluting with a gradient of 5-100% MeOH/DCM