Methanol → HCID 57742524, Verbindung

HRID 2266544Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2266544
C[O:2][C:3](=[O:33])[CH2:4][O:5][C:6]1[CH:15]=[CH:14][C:13]([F:16])=[C:12]2[C:7]=1[C:8]([CH3:32])=[C:9]([CH2:21][C:22]1[CH:27]=[CH:26][C:25]([S:28]([CH3:31])(=[O:30])=[O:29])=[CH:24][CH:23]=1)[C:10]([O:17][CH:18]([F:20])[F:19])=[N:11]2.CO.[OH-].[Li+].O>C(O)(=O)C>[F:20][CH:18]([F:19])[O:17][C:10]1[C:9]([CH2:21][C:22]2[CH:27]=[CH:26][C:25]([S:28]([CH3:31])(=[O:29])=[O:30])=[CH:24][CH:23]=2)=[C:8]([CH3:32])[C:7]2[C:12](=[C:13]([F:16])[CH:14]=[CH:15][C:6]=2[O:5][CH2:4][C:3]([OH:33])=[O:2])[N:11]=1

Komponenten

6

Versuchsvorschrift

A mixture of [2-difluoromethoxy-8-fluoro-3-(4-methanesulfonylbenzyl)-4-methylquinolin-5-yloxy]acetic acid methyl ester (0.57 g), methanol (24 mL), 5.0 M aqueous lithium hydroxide solution (0.5 mL) and water (1.0 mL) was stirred at room temperature for 90 minutes. The pH of the mixture was adjusted to 4 by the addition of glacial acetic acid and the solvent removed under reduced pressure. The residue was diluted with water and the solid collected by filtration, washed with water and dried to afford to title compound as a white solid, 0.53 g.

Aufarbeitung

  1. customthe solvent removed under reduced pressure
  2. additionThe residue was diluted with water
  3. filtrationthe solid collected by filtration
  4. washwashed with water
  5. customdried

Quellen und Nachweise

ORD-Eintrag
ord-0514dd4db473422182e957d42feb5b54
Quelldatensatz
uspto-grants-2010_12
Patentnummer
US07858640B2

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