2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 1,6-Naphthyridin-5(6H)-one, 3-(trifluoromethyl)-

Temperature

100 °C

Into a 100 mL round-bottom flask, was placed a solution of 3-(trifluoromethyl)-7,8-dihydro-1,6-naphthyridin-5(6H)-one (as prepared in the previous step, 1.7 g, 7.87 mmol, 1.00 equiv) in dioxane (20 mL) and 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (2.68 g, 11.81 mmol, 1.50 equiv). The reaction mixture was stirred for 6 h at 100° C. in an oil bath. The resulting mixture was concentrated under vacuum and the residue was dissolved in 20 mL of sodium bicarbonate. The resulting solution was extracted with 3×100 mL of dichloromethane, and the combined organic layers dried over sodium sulfate and concentrated under vacuum. The residue was purified by chromatography over a silica gel column with ethyl acetate/petroleum ether (1:10-1:2). The title compound was obtained as a light yellow solid.

1. customInto a 100 mL round-bottom flask, was placed
2. concentrationThe resulting mixture was concentrated under vacuum
3. dissolutionthe residue was dissolved in 20 mL of sodium bicarbonate
4. extractionThe resulting solution was extracted with 3×100 mL of dichloromethane
5. dry with materialthe combined organic layers dried over sodium sulfate
6. concentrationconcentrated under vacuum
7. customThe residue was purified by chromatography over a silica gel column with ethyl acetate/petroleum ether (1:10-1:2)

ORD record

ord-a2c89940910f4a8c9de4159f95ae6c2d

Source dataset

uspto-grants-2013_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08518969B2