HRID500118

反应详情

EQUATION

反应方程式

HRID 500118 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
110 °C

PROCEDURE

实验过程

A mixture of 1-(4-bromo-3-fluorophenyl)-2,2-diethoxyethanone (15.2 g, 50 mmol), aminoguanidine bicarbonate (10.2 g, 75 mmol) and potassium hydroxide (6.6 g, 100 mmol) in ethanol (200 mL) and water (4 mL) was refluxed overnight. The solvent was evaporated under reduced pressure and the residue was washed with acetonitrile and filtered. The filtrate was concentrated under reduced pressure. The residue was dissolved in dichloromethane (100 mL), washed with water, brine, and concentrated under reduced pressure. The residue was dissolved in ethanol (50 mL). To the solution was added 0.2N hydrochloric acid (50 mL). The resultant mixture was heated to 110° C. for 8 h, and cooled with an ice-water bath. The precipitate that formed was collected by filtration and washed with isopropanol to give the desired product. (5.5 g, 41%) LCMS: (M+H)=286.8/288.8. 1H-NMR (400 MHz, CDCl3): 8.60 (s, 1H), 7.79 (dd, J=8.6, 2.0 Hz, 1H), 7.68 (dd, J=8.3, 7.0 Hz, 1H), 7.61 (dd, J=8.3, 2.0 Hz, 1H), 5.43 (s, 2H).

WORKUP

后处理

  1. temperaturewas refluxed overnight
  2. customThe solvent was evaporated under reduced pressure
  3. washthe residue was washed with acetonitrile
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated under reduced pressure
  6. dissolutionThe residue was dissolved in dichloromethane (100 mL)
  7. washwashed with water, brine
  8. concentrationconcentrated under reduced pressure
  9. dissolutionThe residue was dissolved in ethanol (50 mL)
  10. additionTo the solution was added 0.2N hydrochloric acid (50 mL)
  11. temperaturecooled with an ice-water bath
  12. customThe precipitate that formed
  13. filtrationwas collected by filtration
  14. washwashed with isopropanol