HRID1004001

反应详情

EQUATION

反应方程式

HRID 1004001 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

N,N-Dimethyl formamide (7.9 ml, 0.10 mol) was added dropwise to phosphorus oxychloride (47.9 ml, 0.52 mol) with stirring. After 10 minutes, 4-amino-6-benzyloxy-2-hydroxy-7-methoxyquinazoline (16.4 g, 0.055 mol) was added portionwise and the resulting mixture heated at 90° C. for 1.5 hours, then cooled and poured into ethyl acetate (750 ml). The mixture was neutralised by the portionwise addition of aqueous sodium carbonate and the phases were separated. The organic layer was evaporated to dryness and the residue combined with the organic phase which was then treated with aqueous sodium hydroxide to basify (pH10) and the mixture was heated at 90° C. for 2 hours. After cooling, the mixture was partitioned between dichloromethane (11) and water (11), the organic phase washed with water, dried over MgSO4 and evaporated to give a pale yellow solid. Trituration with isopropanol afforded the subtitle compound as a colourless solid (4.64 g, 27%). Rf 0.64 (ethyl acetate:methanol 95:5, v/v). MS m/z 316, 318 (MH+).

WORKUP

后处理

  1. temperaturecooled
  2. customthe phases were separated
  3. customThe organic layer was evaporated to dryness
  4. additionwas then treated with aqueous sodium hydroxide
  5. temperaturethe mixture was heated at 90° C. for 2 hours
  6. temperatureAfter cooling
  7. customthe mixture was partitioned between dichloromethane (11) and water (11)
  8. washthe organic phase washed with water
  9. dry with materialdried over MgSO4
  10. customevaporated
  11. customto give a pale yellow solid