Acetic Acid → 7H-Naphtho(1,2,3-ij)(2,7)naphthyridin-7-one

Dimethylformamide dimethyl acetal (1.50 mL, 11.34 mmol, Aldrich) was added to a solution of cleistopholine, (1.95 g, 8.73 mmol) in dimethylformamide (5 mL). The mixture was then heated for 30 min by submerging the reaction vessel into an oil bath preheated to 120° C. At this point, ammonium chloride (4.5 g) and glacial acetic acid (15 mL) were added to the reaction and the heating (120° C.) continued for an additional 30 min. After allowing to cool, the reaction was poured onto water (200 mL) and partitioned with methylene chloride (5×100 mL). The combined organic phases were washed with saturated sodium bicarbonate solution (3×100 mL), water (3×100 mL), dried over potassium carbonate, and concentrated to dryness. The residual dark brown solids were chromatographed on silica gel (4×70 cm column, Merck 230-400 mesh) while eluting with ethyl acetate. Concentration of the appropriate column fractions provided pure sampangine (1.60 g, 79 %), mp 220-222 (lit. mp 216°-218° C.). IR 1670, 1615, 1590, 1400, 1380, 1320, 1275, 1225, 760, 725 cm-1 ; 1H and 13C NMR.

1. temperatureThe mixture was then heated for 30 min
2. custompreheated to 120° C
3. temperatureto cool
4. additionthe reaction was poured onto water (200 mL)
5. custompartitioned with methylene chloride (5×100 mL)
6. washThe combined organic phases were washed with saturated sodium bicarbonate solution (3×100 mL), water (3×100 mL)
7. dry with materialdried over potassium carbonate
8. concentrationconcentrated to dryness
9. customThe residual dark brown solids were chromatographed on silica gel (4×70 cm column, Merck 230-400 mesh)
10. washwhile eluting with ethyl acetate

ORD-Eintrag

ord-e82a6c84271c40c588f213f956bcef5b

Quelldatensatz

uspto-grants-1996_06

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05530004