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
- 100 °C
PROCEDURE
实验过程
A mixture of diethyl[4-({4-[(7-bromo-2-methyl-3-oxo-2,3-dihydro-1H-isoindol-4-yl)amino]-5-(trifluoromethyl)pyrimidin-2-yl}amino)benzyl]phosphonate (200.0 mg, 0.3183 mmol), piperazine-1-acetic acid tert-butyl ester (382 mg, 1.91 mmol), bis(dibenzylideneacetone)palladium (58.29 mg, 0.06366 mmol), 2,2′-bis-diphenylphosphanyl-[1,1′]binaphthalenyl (118.9 mg, 0.1910 mmol), Cs2CO3 (0.3111 g, 0.9548 mmol) in 1,4-dioxane (20 mL) was evacuated and purged with nitrogen three times. The mixture was stirred at 100° C. for 2 days. The crude mixture was purified by MDP. The purified ester was taken up in methylene chloride (1.2 mL) and trifluoroacetic acid (0.6 mL) and the mixture was stirred at room temperature for 3 hours. The crude product was purified by MDP to obtain the title compound as a trifluoroacetic acid salt. 1H NMR (400 MHz, methanol-d4) δ=1.27 (t, J=7.1 Hz, 6H), 3.19 (s, 3H), 3.29 (d, J=21.5 Hz, 2H), 3.41 (br. s., 4H), 3.60 (br. s., 4H), 4.07 (qd, J=7.2, 6.9 Hz, 4H), 4.17 (s, 2H), 4.51 (s, 2H), 7.26 (d, J=9.1 Hz, 1H), 7.34 (d, J=6.6 Hz, 2H), 7.57 (d, J=7.8 Hz, 2H), 8.36 (s, 1H), 8.69 (br. s., 1H). MS (ES+): m/z 692.27 (100) [MH+]; HPLC: tR=0.78 min (UPLC, purity).
WORKUP
后处理
- customwas evacuated
- custompurged with nitrogen three times
- customThe crude mixture was purified by MDP
- stirringtrifluoroacetic acid (0.6 mL) and the mixture was stirred at room temperature for 3 hours
- customThe crude product was purified by MDP