反应详情

To a suspension of 7-hydroxy-6-methoxy-4-(quinolin-7-yloxy)quinazoline (450 mg, 1.40 mmol), (prepared as described in Example 197), in DMF (50 ml) was added anhydrous potassium carbonate (773 mg, 5.60 mmol) and 4-(2-hydroxyethyl)morpholine (335 mg, 1.80 mmol), and the reaction heated under reflux for 2 hours. The DMF was evaporated in vacuo, and the residue partitioned between dichloromethane and 1N aqueous sodium hydroxide. The mixture was extracted with dichloromethane (3×200 ml), dried (MgSO4) and concentrated in vacuo. The crude product was triturated with hexane/ether to afford a solid which was filtered and dried under suction to give 6-methoxy-7-(2-morpholinoethoxy)-4-(quinolin-7-yloxy)quinazoline (430 mg, 1.00 mmol, 71%) as a light brown solid.

1. temperaturethe reaction heated
2. temperatureunder reflux for 2 hours
3. customThe DMF was evaporated in vacuo
4. customthe residue partitioned between dichloromethane and 1N aqueous sodium hydroxide
5. extractionThe mixture was extracted with dichloromethane (3×200 ml)
6. dry with materialdried (MgSO4)
7. concentrationconcentrated in vacuo
8. customThe crude product was triturated with hexane/ether
9. customto afford a solid which
10. filtrationwas filtered
11. customdried under suction