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
- 120 °C
PROCEDURE
实验过程
To a degassed solution 6-((6-bromo-1H-[1,2,3]triazolo[4,5-b]pyrazin-1-yl)methyl)quinoline (1200 mg, 3.52 mmol) in DMF (10 mL), was added Pd(PPh3)4 (610 mg, 0.528 mmol). The solution was stirred for 20 min, then tributyl(vinyl)stannane (1227 mg, 3.87 mmol) was added. The reaction mixture was heated to 120° C. for 5 h. NH4Cl(aq) was added to quench the reaction, followed by EtOAc. The reaction mixture was filtered through celite and the filtrate was washed with sat NaHCO3, sat NH4Cl. The organic layer was separated, dried over Na2SO4 and concentrated to give the crude product, which was purified with Analogix gel silica (Hexanes:EA) to afford 210 mg of title compound in 20% yield. LCMS (method B): [MH]+=288, tR=2.05 min.
WORKUP
后处理
- customto quench
- customthe reaction
- filtrationThe reaction mixture was filtered through celite
- washthe filtrate was washed with sat NaHCO3
- customThe organic layer was separated
- dry with materialdried over Na2SO4
- concentrationconcentrated
- customto give the crude product, which
- customwas purified with Analogix gel silica (Hexanes:EA)