Tetrahydrofuran → 2,4-dimethoxy-7-(4-methoxy-3,5-dimethylphenyl)-1,6-naphthyridin-5(6H)-one

HRID 1498700

Reaktionsgleichung

Reaktionsgleichung von HRID 1498700
[CH3:1][O:2][C:3]1[C:8]([C:9]([NH2:11])=[O:10])=[C:7]([CH3:12])[N:6]=[C:5]([O:13][CH3:14])[CH:4]=1.C([Li])CCC.CO[C:22]1C=[CH:28][C:25]([C:26]#N)=[CH:24][CH:23]=1.[CH2:30]1[CH2:34][O:33][CH2:32][CH2:31]1>>[CH3:14][O:13][C:5]1[CH:4]=[C:3]([O:2][CH3:1])[C:8]2[C:9](=[O:10])[NH:11][C:28]([C:25]3[CH:24]=[C:23]([CH3:22])[C:34]([O:33][CH3:32])=[C:30]([CH3:31])[CH:26]=3)=[CH:12][C:7]=2[N:6]=1

Komponenten

5

Edukt 4

HCID 8028Tetrahydrofuran2×HCID 701294-MethoxybenzonitrileHCID 666614724,6-Dimethoxy-2-methyl-nicotinamideHCID 178418339Butyllithium

Produkt 1

HCID 249597052,4-dimethoxy-7-(4-methoxy-3,5-dimethylphenyl)-1,6-naphthyridin-5(6H)-oneAusbeute 12 %

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of 4,6-dimethoxy-2-methyl nicotinamide (2.0 g, 10.2 mmol) in THF (80 mL), n-butyl lithium (19.12 mL, 30.6 mmol, 1.6 M solution in hexane) was added slowly under nitrogen at −78° C. After completion of addition the mixture was stirred for 1 h at 0° C. Then cooled to −78° C. and a solution of 4-methoxy benzonitrile (1.65 g, 10.2 mmol) in THF (10 mL) was added quickly. The cooling bath was removed and the reaction mixture was allowed to warm to room temperature and stirred for 16 h at room temperature. Saturated NH4Cl solution was added with cooling. The organic layer was washed with water, brine, dried over Na2SO4 and concentrated to give crude product. The crude product was purified by chromatography using 50% ethyl acetate in hexane and then 2% methanol in ethyl acetate to give 2,4-dimethoxy-7-(4-methoxy-3,5-dimethylphenyl)-1,6-naphthyridin-5(6H)-one (410 mg, 12%), as a yellow solid. Selected data: MS (ES) m/z: 341.1; mp 262-263° C. (at decomposition).

Aufarbeitung

  1. additionAfter completion of addition the mixture
  2. temperatureThen cooled to −78° C.
  3. customThe cooling bath was removed
  4. temperatureto warm to room temperature
  5. stirringstirred for 16 h at room temperature
  6. additionSaturated NH4Cl solution was added
  7. temperaturewith cooling
  8. washThe organic layer was washed with water, brine
  9. dry with materialdried over Na2SO4
  10. concentrationconcentrated
  11. customto give crude product
  12. customThe crude product was purified by chromatography

Quellen und Nachweise

ORD-Eintrag
ord-da42ee9703ec450fb9a191dc415d2ba0
Quelldatensatz
uspto-grants-2015_12
Patentnummer
US09199990B2

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