HRID221529

反应详情

EQUATION

反应方程式

HRID 221529 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
-78 °C

PROCEDURE

实验过程

1-[(1S)-1-({[tert-Butyl(dimethyl)silyl]oxy}methyl)-2-methylpropyl]-2-(chloromethyl)-1H-imidazo[4,5-c]quinoline (4.85 g, 11.6 mmol) was dissolved in 110 mL of tetrahydrofuran (THF) and the solution was cooled to −78° C. under N2. A 1.0 M solution of tetrabutylammonium fluoride in THF (12.8 mL) was added and the reaction mixture was allowed to warm to 0° C. overnight. The reaction mixture was then treated with 50 mL of saturated sodium bicarbonate solution and 100 mL of CHCl3. The layers were separated and the organic portion was washed with H2O (50 mL) and brine (4×25 mL). The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure to give a yellow syrup. The syrup was concentrated from toluene (3×) to give a pale yellow foam. This material was dissolved in 100 mL of anhydrous THF and the solution was cooled 0° C. and stirred under N2. Solid potassium tert-butoxide was then added and the reaction mixture was allowed to warm to ambient overnight. The THF was then removed under reduced pressure and the resulting material was partitioned between 100 mL of CHCl3 and 100 mL of saturated sodium bicarbonate solution. The layers were separated and the organic portion was washed with H2O and brine. The organic portion was then dried over Na2SO4, filtered and concentrated under reduced to give brown foam. Chromatography (SiO2, 0%-50% 80:18:2 CHCl3/methanol/concentrated NH4OH(CMA) in CHCl3) gave (11S)-11-isopropyl-10,11-dihydro-8H-[1,4]oxazino[4′,3′:1,2]imidazo[4,5-c]quinoline (2.13 g) as a light yellow solid.

WORKUP

后处理

  1. temperatureto warm to 0° C. overnight
  2. customThe layers were separated
  3. washthe organic portion was washed with H2O (50 mL) and brine (4×25 mL)
  4. dry with materialThe organic layer was dried over Na2SO4
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customto give a yellow syrup
  8. concentrationThe syrup was concentrated from toluene (3×)
  9. customto give a pale yellow foam
  10. temperaturethe solution was cooled 0° C.
  11. temperatureto warm to ambient overnight
  12. customThe THF was then removed under reduced pressure
  13. customthe resulting material was partitioned between 100 mL of CHCl3 and 100 mL of saturated sodium bicarbonate solution
  14. customThe layers were separated
  15. washthe organic portion was washed with H2O and brine
  16. dry with materialThe organic portion was then dried over Na2SO4
  17. filtrationfiltered
  18. concentrationconcentrated
  19. customto give brown foam