反应详情

To a solution of N-(3-chloropyridin-2-yl)-4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-2-carboxamide in acetonitrile (0.702 ml) was added hexamethyldisilazane (0.029 ml, 0.140 mmol) and heated at reflux for 3 hours. Chloro(chloromethyl)dimethylsilane (0.029 ml, 0.224 mmol) was added to the refluxing solution drop-wise and the reaction mixture was refluxed overnight. Next, the reaction mixture was equilibrated to room temperature and concentrated to a solid residue. This solid was taken into diglyme (2 ml, 10 mmol) and treated with cesium fluoride (0.21 g, 1.4 mmol) at reflux for 3 hours. The reaction mixture was cooled to room temperature and diluted with water and ethyl acetate. The organic was separated from the aqueous in a separatory funnel. The organic was washed with saline, dried (Na2SO4) and concentrated to a solid. This crude material was taken into methanol at 100 mg/ml and purified by RP-HPLC to give 24 mg of 207, 29% of theoretical yield. MS: (ESI+) 371.1

1. temperatureheated
2. temperatureat reflux for 3 hours
3. temperaturethe reaction mixture was refluxed overnight
4. customwas equilibrated to room temperature
5. concentrationconcentrated to a solid residue
6. temperatureat reflux for 3 hours
7. customThe organic was separated from the aqueous in a separatory funnel
8. washThe organic was washed with saline
9. dry with materialdried (Na2SO4)
10. concentrationconcentrated to a solid
11. custompurified by RP-HPLC