Reaktion #1154447

ord-08d4ee58617144af92d5be7d2fe9e9a7

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto precipitate the product
  2. 2
    SonstigeThe solid is collected
  3. 3
    Sonstigechromatographed (1% MeOH in CH2Cl2 (2L))
  4. 4
    Einengenconcentrated

Vorschrift

To a solution of N-(4-chlorobenzyl)-8-fluoro-4-hydroxy-6-(4-morpholinylmethyl)-3-quinolinecarboxamide, (can be prepared according to the procedure described in PCT patent application, W099/32450) (147 mg) in anhydrous DMF (3 mL) is added K2CO3 (71.2 mg) followed by CH3I (0.026 mL). The reaction mixture is stirred at room temperature for 30 min, then poured into H2O (40 mL) to precipitate the product. The solid is collected, adsorbed onto silica, and chromatographed (1% MeOH in CH2Cl2 (2L)). Fractions homogenous by TLC are combined and concentrated to afford 55.3 mg of the title compound as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06248736B1uspto-grants-2001_06