反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 150 °C
PROCEDURE
实验过程
A mixture of 6-((2R,6R)-2,6-dimethylmorpholino)-7-fluoro-3-(1-methyl-1H-1,2,4-triazol-5-yl)benzo[d]isoxazole-5-carbaldehyde (Intermediate 537, 124 mg, 0.35 mmol) and pyrimidine-2,4,6(1H,3H,5H)-trione (44.2 mg, 0.35 mmol) in methanol (3 ml) was heated at 150° C. for 1 hour in a microwave reactor. Solvent was removed and the residue was purified by reverse phase HPLC (CH3CN/water gradient with 0.1% TFA). The solid was taken up in 9:1 CH2Cl2— MeOH and washed with NaHCO3 and brine. The aqueous layers were repeatedly extracted with additional 9:1 CH2Cl2-MeOH with each extract being washed with brine. The combined organic layers were dried (MgSO4) and concentrated and the residue was dissolved in THF. After removal of solvent, the solid residue was dried in vacuo at 50° C. overnight to afford desired product.
WORKUP
后处理
- customSolvent was removed
- customthe residue was purified by reverse phase HPLC (CH3CN/water gradient with 0.1% TFA)
- washwashed with NaHCO3 and brine
- extractionThe aqueous layers were repeatedly extracted with additional 9:1 CH2Cl2-MeOH with each extract
- washbeing washed with brine
- dry with materialThe combined organic layers were dried (MgSO4)
- concentrationconcentrated
- dissolutionthe residue was dissolved in THF
- customAfter removal of solvent
- customthe solid residue was dried in vacuo at 50° C. overnight