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
- 85 °C
PROCEDURE
实验过程
2-Amino-4-chloro-thieno[2,3-d]pyrimidine-6-carboxylic acid ethyl ester (7.62 g, 29.57 mmol) was added to 4-Methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzaldehyde (7.28 g, 29.57 mmol) followed by sodium hydrogen carbonate (7.45 g, 88.71 mmol). DMF (110 mL) was added followed by water (22 mL) and the suspension was degassed by evacuation—nitrogen purge (3 cycles), followed by bubbling nitrogen gas through the stirred reaction mixture for 5 minutes. Bis(triphenylphosphine)palladium (II) chloride (500 mg, 0.739 mmol) was added and reaction mixture was heated to 85 degrees C. (oil-bath temperature) for 18 hours. Reaction mixture was allowed to cool to room temperature and DMF removed in vacuo. The residue was partitioned between ethyl acetate (500 mL) and water (400 mL) and the mixture was stirred vigorously for 15 min before being filtered through a pad of celite to remove Pd solids. Filter cake was washed with ethyl acetate (2×50 mL) and combined filtrate phases were separated and the organic phase was washed with water (1×300 mL) then saturated sodium chloride solution (250 mL). Organic phase was dried over Na2SO4 and filtered, and filtrate solvents removed in vacuo to afford a brown oily solid which was triturated with ethyl acetate to afford product as a brown solid (5.42 g, 56%)
WORKUP
后处理
- customthe suspension was degassed by evacuation—nitrogen
- custompurge (3 cycles)
- customby bubbling nitrogen gas
- customthrough the stirred reaction mixture for 5 minutes
- customreaction mixture
- customReaction mixture
- temperatureto cool to room temperature
- customDMF removed in vacuo
- customThe residue was partitioned between ethyl acetate (500 mL) and water (400 mL)
- filtrationbefore being filtered through a pad of celite
- customto remove Pd solids
- filtrationFilter cake
- washwas washed with ethyl acetate (2×50 mL)
- customwere separated
- washthe organic phase was washed with water (1×300 mL)
- dry with materialOrganic phase was dried over Na2SO4
- filtrationfiltered
- customfiltrate solvents removed in vacuo
- customto afford a brown oily solid which
- customwas triturated with ethyl acetate