HRID1506421

反应详情

EQUATION

反应方程式

HRID 1506421 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

4

PROCEDURE

实验过程

To a solution of 3-phenyl-4-(trifluoromethyl)-5-(7-vinyl-4,5-dihydronaphtho[2,1-d]thiazol-2-yl)isoxazole (Preparation 56E, 0.350 g, 0.825 mmol) in THF (7.5 ml) at room temperature, was added a solution of osmium tetroxide, (2.5% in butanol, 1.7 ml, 0.017 mmol) followed by sodium periodate (0.265 g, 1.238 mmol) as a solution in 7.5 ml of water. After stirring for 90 min it was quenched with a saturated solution of sodium bisulfate. The dark colored suspension was filtered through Celite. The filter cake was washed with EtOAc. The combined EtOAc layers were washed with water, dried over anhydrous MgSO4, concentrated, and chromatographed to yield the 2-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-4,5-dihydronaphtho[2,1-d]thiazole-7-carbaldehyde as an orange colored solid. The product had an LC ret. time=3.136 min. (condition: Start % B=50, Final % B=100, Gradient Time=4 min, Flow Rate=4 ml/min, Wavelength=220, Solvent Pair=MeOH−H2O−TFA; Solvent A=10% MeOH−90% H2O−0.1% TFA; Solvent B=90% MeOH−10% H2O−0.1% TFA; Column 1=1: Waters Sunfire C18 4.6×50 mm (4 min. grad)); LC/MS M+1=427.03.

WORKUP

后处理

  1. customwas quenched with a saturated solution of sodium bisulfate
  2. filtrationThe dark colored suspension was filtered through Celite
  3. washThe filter cake was washed with EtOAc
  4. washThe combined EtOAc layers were washed with water
  5. dry with materialdried over anhydrous MgSO4
  6. concentrationconcentrated
  7. customchromatographed