Imidazole → 6-Imidazol-1-yl-3,4-dihydro-1H-quinolin-2-one

HRID 414566

Reaktionsgleichung

Reaktionsgleichung von HRID 414566
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][C:7](=[O:12])[CH2:6][CH2:5]2.[NH:13]1[CH:17]=[CH:16][N:15]=[CH:14]1.C(=O)([O-])[O-].[K+].[K+].O>CN(C)C=O>[N:13]1([C:2]2[CH:3]=[C:4]3[C:9](=[CH:10][CH:11]=2)[NH:8][C:7](=[O:12])[CH2:6][CH2:5]3)[CH:17]=[CH:16][N:15]=[CH:14]1

Komponenten

6

Edukt 4

HCID 795ImidazoleHCID 962WaterHCID 11430Potassium CarbonateHCID 143732816-Bromo-3,4-dihydroquinolin-2(1H)-one

Produkt 1

HCID 138852786-Imidazol-1-yl-3,4-dihydro-1H-quinolin-2-one

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

A mixture of 1.0 g of 6-bromo-3,4-dihydrocarbostyril, 300 mg of imidazole, 40 mg of cuprous iodide and 600 mg of potassium carbonate in 4 ml of N,N-dimethylformamide was heated at 90° C. for 48 hours. The reaction mixture was poured into water and extracted with a mixture of 10% methanol in methylene chloride. The organic layer was dried over anhydrous sodium sulfate, the solvent removed under reduced pressure and the residue chromatographed on silica gel, eluting with 3% methanol in methylene chloride, giving 6-(imidazol-1-yl)-3,4-dihydrocarbostyril, m.p. 205°-208° C.

Aufarbeitung

  1. extractionextracted with a mixture of 10% methanol in methylene chloride
  2. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  3. customthe solvent removed under reduced pressure
  4. customthe residue chromatographed on silica gel
  5. washeluting with 3% methanol in methylene chloride

Quellen und Nachweise

ORD-Eintrag
ord-27e879c29d4640c7b7574a0baa43f3ed
Quelldatensatz
uspto-grants-1988_12
Patentnummer
US04792561

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