Potassium Carbonate → 7-bromo-5-(2-chloro-4-fluorophenyl)-1-(2,6-dichlorophenyl)-3,4-dihydro-1,6-naphthyridin-2(1H)-one

Temperatur

155 °C

To 3-[4,6-dibromo-2-(2-chloro-4-fluorophenyl)pyridin-3-yl]-N-(2,6-dichlorophenyl)propanamide (3.14 g, 5.40 mmol) in DMF (50 mL) was added K2CO3 (1.49 g, 10.8 mmol) and CuI (1.54 g, 10.8 mmol). The resulting reaction mixture was evacuated and purged with argon 3 times, and then heated at 155° C. (oil bath) for 35 min. The reaction mixture was cooled to rt and diluted with 240 mL of half-saturated aqueous NaHCO3 and 120 mL of ethyl acetate. The layers were separated and the aqueous layer was extracted with 2×180 mL of ethyl acetate. The combined organic layers were washed with 120 mL of brine, dried over Na2SO4, and concentrated under reduced pressure. The product was purified by flash chromatography on 2 Biotage 40M columns, eluting with 50:50 hexanes-CH2Cl2 to yield 7-bromo-5-(2-chloro-4-fluorophenyl)-1-(2,6-dichlorophenyl)-3,4-dihydro-1,6-naphthyridin-2(1H)-one. Mass spectrum (ESI) 499.2 (M+1).

1. customThe resulting reaction mixture
2. customwas evacuated
3. custompurged with argon 3 times
4. temperatureThe reaction mixture was cooled to rt
5. additiondiluted with 240 mL of half-saturated aqueous NaHCO3 and 120 mL of ethyl acetate
6. customThe layers were separated
7. extractionthe aqueous layer was extracted with 2×180 mL of ethyl acetate
8. washThe combined organic layers were washed with 120 mL of brine
9. dry with materialdried over Na2SO4
10. concentrationconcentrated under reduced pressure
11. customThe product was purified by flash chromatography on 2 Biotage 40M columns
12. washeluting with 50:50 hexanes-CH2Cl2

ORD-Eintrag

ord-d8e60045b6bb4edcb5b2d4587095ea74

Quelldatensatz

uspto-grants-2004_10

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US06809199B2