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 1-(7-bromo-4-methoxy-1H-pyrrolo[2,3-c]pyridin-3-yl)-2-(5-(pyridin-2-yl)-3,4-dihydroisoquinolin-2(1H)-yl)ethane-1,2-dione (100 mg, 0.204 mmol), 3-(trifluoromethyl)-1H-pyrazole (55.4 mg, 0.407 mmol), (1R,2S)—N1,N2-dimethylcyclohexane-1,2-diamine (5.79 mg, 0.041 mmol), copper(I) iodide (19.38 mg, 0.102 mmol) and potassium carbonate (84 mg, 0.611 mmol) in dioxane (1 mL) was heated up at 100° C. for 36 hours. LCMS indicated desired product was formed. The reaction mixture was filtered and the clear solution was dissolved in methanol and purified by prep. HPLC to give 1-(4-methoxy-7-(3-(trifluoromethyl)-1H-pyrazol-1-yl)-1H-pyrrolo[2,3-c]pyridin-3-yl)-2-(5-(pyridin-2-yl)-3,4-dihydroisoquinolin-2(1H)-yl)ethane-1,2-dione as white solid (37 mg, 32%). LCMS: m/e 547.05 (M+H)+, 2.17 min (method 9). 1H NMR (500 MHz, MeOD) δ ppm 2.85-3.09 (m, 2H) 3.74-3.99 (m, 5H) 4.84 (s, 1H) 5.04 (s, 1H) 6.94 (d, J=2.44 Hz, 1H) 7.36-7.67 (m, 3H) 7.80-7.88 (m, 1H) 7.97-8.16 (m, 2H) 8.31-8.40 (m, 1H) 8.52-8.67 (m, 1H) 8.79 (s, 1H) 8.84-8.96 (m, 1H).