HRID25516

反应详情

EQUATION

反应方程式

HRID 25516 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
40 °C

PROCEDURE

实验过程

In acetone (50 mL) was placed 5-(1H-indol-2-yl)-2-methoxy-phenylamine (2.38 g, 10 mmol). To this was added potassium carbonate (5.53 g, 40 mmol), and to the vigorously stirred mixture was added methyl iodide (1.55 g, 11 mmol). The mixture warmed to 40° C. and stirred for 48 hours. The mixture cooled to room temperature and was filtered free of inorganics. The resulting solution was evaporated in vacuo to give a solid which was partitioned between ethyl acetate (50 mL) and water (50 mL). The organic phase was separated, dried over magnesium sulfate, and evaporated in vacuo to give a tan solid. This solid was purified by flash chromatography over silica gel (5% ethyl acetate/methylene chloride). Evaporation of the appropriate fractions gave 0.68 g of pure compound. MS: M+1=253.1. 1H NMR (DMSO-d6) δ 2.79 (d, J=5.3 Hz, 3H), 3.80 (s, 3H), 5.08-5.12 (m, 1H), 6.69 (s, 1H), 6.83-7.05 (m, 5H), 7.33 (d, J=7.9 Hz, 1H), 7.44 (d, J=8.0 Hz, 1H), 11.28 (s, 1H) ppm.

WORKUP

后处理

  1. temperatureThe mixture cooled to room temperature
  2. filtrationwas filtered free of inorganics
  3. customThe resulting solution was evaporated in vacuo
  4. customto give a solid which
  5. customwas partitioned between ethyl acetate (50 mL) and water (50 mL)
  6. customThe organic phase was separated
  7. dry with materialdried over magnesium sulfate
  8. customevaporated in vacuo
  9. customto give a tan solid
  10. customThis solid was purified by flash chromatography over silica gel (5% ethyl acetate/methylene chloride)
  11. customEvaporation of the appropriate fractions