Potassium Hydroxide → 3-Methyl-6-(methylthio)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

HRID 245152Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 245152
[OH-:1].[K+].[CH3:3][S:4][C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][CH:13]=1)[NH:10][C:9](=[O:14])[C:8]2=O.[F:16][C:17]([F:29])([F:28])[C:18]1[CH:19]=[C:20]([C:24](=O)[CH2:25][CH3:26])[CH:21]=[CH:22][CH:23]=1>O.C(O)C>[CH3:26][C:25]1[C:24]([C:20]2[CH:21]=[CH:22][CH:23]=[C:18]([C:17]([F:16])([F:28])[F:29])[CH:19]=2)=[N:10][C:11]2[C:7]([C:8]=1[C:9]([OH:14])=[O:1])=[CH:6][C:5]([S:4][CH3:3])=[CH:13][CH:12]=2

Komponenten

6

Versuchsvorschrift

Potassium hydroxide (3.31 g, 59.0 mmol) in water (10 mL) was added slowly to a suspension of 5-(methylthio)-1H-indole-2,3-dione (1.9 g, 9.83 mmol) in ethanol (25 mL). 1-[3-(Trifluoromethyl)phenyl]-1-propanone (1.99 g, 9.83 mmol) was added and the mixture was heated to reflux for 1 h. The solvent was removed under reduced pressure, the residue was dissolved in water, and the aqueous mixture was washed with ether (3 times). The aqueous phase was chilled and was acidified to pH 3 with concentrated HCl. The solid material was collected by filtration, washed with water, and air dried to afford 3-methyl-6-(methylthio)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid (2.5 g, 67% yield). MS (m/z) 378.0 (M+H+).

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 1 h
  3. customThe solvent was removed under reduced pressure
  4. dissolutionthe residue was dissolved in water
  5. washthe aqueous mixture was washed with ether (3 times)
  6. temperatureThe aqueous phase was chilled
  7. filtrationThe solid material was collected by filtration
  8. washwashed with water, and air
  9. customdried

Quellen und Nachweise

ORD-Eintrag
ord-20820fad8d1647319b9ca15de2fd2c09
Quelldatensatz
uspto-grants-2014_02
Patentnummer
US08658636B2

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