反应详情

0.25 g of 4-(3,4-dihydro-2H-quinolin-1-yl)-6-(1H-pyrrolo[2,3-b]pyridin-5-yl)-quinazoline, 0.31 g of 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridine, 0.16 g of sodium hydrogencarbonate and 90 mg of PdCl2(PPh3)2 in 5.00 ml of dioxane and 0.50 ml of water are heated at 90° C. under nitrogen in a flask until the reaction is complete (HPLC check, about 18 hours). The cooled reaction solution is diluted with EA and washed 3 times with water. The organic phase is dried over sodium sulfate and purified by means of column chromatography (gradient heptane: EA 5-100% in 16 min), giving 0.20 g of 4-(3,4-dihydro-2H-quinolin-1-yl)-6-(1-triisopropylsilanyl-1H-pyrrolo[2,3-b]pyridin-5-yl)-quinazoline as yellow oil (yield 50%, content 83%).

1. custom(HPLC check, about 18 hours)
2. customThe cooled reaction solution
3. washwashed 3 times with water
4. dry with materialThe organic phase is dried over sodium sulfate
5. custompurified by means of column chromatography (gradient heptane: EA 5-100% in 16 min)