反应详情

In a dry 25 mL round bottom flask, 7-(2-chloro-5-methoxy-phenyl)-5-methyl-benzo[1,2,4]triazin-3-ylamine (0.113 g, 0.377 mmol, 1 equiv), 1-[2-(3-bromo-phenoxy)-ethyl]-pyrrolidine (0.153 g, 0.565 mmol, 1.5 equiv), cesium carbonate (0.368 g, 1.13 mmol, 3 equiv), 4,5-bis(diphenylphosphino)-9,9-dimethyl xanthene (0.044 g, 0.0753 mmol, 0.2 equiv) and tris(dibenzylideneacetone)dipalladium (0.034 g, 0.0376 mmol, 0.1 equiv) were combined. The reactants were flushed with argon, diluted with dioxane (8 mL) and outfitted with reflux condenser. The reaction was heated to reflux for 18 hours, then filtered hot and the solvents were diluted with ethyl acetate and washed with brine. The brine layer was back extracted once with fresh ethyl acetate. The organic phases were combined and dried over sodium sulfate (Na2SO4). Filtration followed by evaporation and column chromatography (1:5 MeOH/DCM) provided desired product as a yellow powder (0.12 g, 65% yield). MS (ESI+): m/z=491.1, LC retention time: 2.94 min.

1. customThe reactants were flushed with argon
2. additiondiluted with dioxane (8 mL)
3. temperaturewith reflux condenser
4. temperatureThe reaction was heated
5. temperatureto reflux for 18 hours
6. filtrationfiltered hot
7. additionthe solvents were diluted with ethyl acetate
8. washwashed with brine
9. extractionThe brine layer was back extracted once with fresh ethyl acetate
10. dry with materialdried over sodium sulfate (Na2SO4)
11. filtrationFiltration
12. customfollowed by evaporation and column chromatography (1:5 MeOH/DCM)