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
- 80 °C
PROCEDURE
实验过程
The product from step 4 (150 mg, 0.32 mmol) and Intermediate C (138 mg, 0.41 mmol) were dissolved in 2 mL of 1:1-toluene:dioxane and degassed with a vacuum/N2 purge sequence (3×). 1,1′-Bis(diphenylphosphino)ferrocenepalladium(II) chloride-complex with methylene chloride (12 mg, 0.02 mmol) was added followed by 1 mL of 2M aqueous Na2CO3 solution and the mixture heated to 80° C. overnight. The heating bath was removed and the mixture diluted with water and EtOAc (5 mL each). The layers were separated and the aqueous phase was extracted with EtOAc and the combined organic phases were washed with water and brine, dried (Na2SO4), filtered and concentrated in, vacuo. The residue was purified by Isco® (Red-sep 12 eluting with 70%—100% EtOAc/hexanes) to give 77 mg (40%) of the title compound as a tan solid. 1H-NMR (DMSO-d6) 8.33 (s, 1H), 7.61 (s, 1H), 7.57 (bs, 2H), 7.40-7.24 (m, 7H), 7.22 (s, 1H), 7.08, (d, 1H), 7.06 (s, 1H), 6.77 (d, 1H), 6.58 (d, 1H), 6.25 (d, 1H), 5.55 (s, 2H), 3.47 (m, 4H), 3.18 (m, 4H), 1.42 (s, 9H); LC-MS [M+H]+=601.3, RT=3.12 min.
WORKUP
后处理
- custom1-toluene:dioxane and degassed with a vacuum/N2
- custompurge sequence (3×)
- customThe heating bath was removed
- additionthe mixture diluted with water and EtOAc (5 mL each)
- customThe layers were separated
- extractionthe aqueous phase was extracted with EtOAc
- washthe combined organic phases were washed with water and brine
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated in, vacuo
- customThe residue was purified by Isco® (Red-sep 12 eluting with 70%—100% EtOAc/hexanes)