反应详情

To a mixture of 4-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)-N,N-dimethylbut-3-en-1-amine (234) (171 mg, 0.44 mmol) and NH4Cl (20 mg, 0.37 mmol) in EtOH (4.4 mL)/water (2.2 mL) at 100° C., Fe (209 mg, 3.75 mmol) was added in one portion and the mixture was heated to reflux with vigorous stirring for 40 min. The mixture was filtered through Celite®, the Celite® washed with EtOH and the combined organic solutions concentrated under reduced pressure. The residue was dissolved in MeOH and purified by preparative HPLC (gradient 40% to 95% MeOH in water, 45 min) giving title compound 235 as a yellow solid (122.8 mg, 0.3 mmol, 69% yield). MS (m/z): (M+1) 358.1 (100%).

1. temperaturethe mixture was heated
2. temperatureto reflux
3. filtrationThe mixture was filtered through Celite®
4. washthe Celite® washed with EtOH
5. concentrationthe combined organic solutions concentrated under reduced pressure
6. dissolutionThe residue was dissolved in MeOH
7. custompurified by preparative HPLC (gradient 40% to 95% MeOH in water, 45 min)