Water → 4-Oxo-4,5-dihydrothieno[2,3-c]quinoline-7-carbonitrile

HRID 1919673Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1919673
CO[C:3]([C:5]1[S:6][CH:7]=[CH:8][C:9]=1Br)=[O:4].Cl.[NH2:12][C:13]1[CH:18]=[C:17]([C:19]#[N:20])[CH:16]=[CH:15][C:14]=1B(O)O.C(=O)([O-])[O-].[Cs+].[Cs+].O>O1CCOCC1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[O:4]=[C:3]1[C:5]2[S:6][CH:7]=[CH:8][C:9]=2[C:14]2[CH:15]=[CH:16][C:17]([C:19]#[N:20])=[CH:18][C:13]=2[NH:12]1

Komponenten

7

Versuchsvorschrift

Methyl-3-bromothiophene carboxylate (1.0 eq, 2.42 g, 10.95 mmol), 2-amino-4-cyanophenylboronic acid hydrochloride (1.05 eq, 2.28 g, 11.49 mmol) and cesium carbonate (2.0 eq, 7.13 g, 21.9 mmol) were suspended in dioxane (25 ml) containing 5% water. The mixture was degassed by bubbling nitrogen for 10 minutes. PdCl2(dppf) (0.05 eq, 400 mg, 0.55 mmol) was added and the mixture was stirred at reflux for 1.5 hours. The mixture was cooled down, the solid filtered, washed with dioxane, water and methanol. After drying in vacuo, 4-oxo-4,5-dihydrothieno[2,3-c]quinoline-7-carbonitrile was isolated as a solid (1.81 g, 73% yield). LCMS (ES) m/z 227 [M+1]+.

Aufarbeitung

  1. customThe mixture was degassed
  2. customby bubbling nitrogen for 10 minutes
  3. temperatureat reflux for 1.5 hours
  4. temperatureThe mixture was cooled down
  5. filtrationthe solid filtered
  6. washwashed with dioxane, water and methanol
  7. customAfter drying in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-bb101d80efe34071a394b2d19a9673fe
Quelldatensatz
uspto-grants-2012_05
Patentnummer
US08168651B2

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