Reaktion #11867

ord-71202caef48949bf8ff4e43739e43746

Lösungsmittel

Reaktionsbedingungen

Temperatur
120°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigequenched with 2 N aqueous sodium hydroxide solution
  2. 2
    SonstigeThe organic layer was separated
  3. 3
    Waschensuccessively washed with water (10 mL) and brine (10 mL)
  4. 4
    Trocknendried over anhydrous sodium sulfate
  5. 5
    Filtrationfiltered
  6. 6
    Einengenconcentrated in vacuo
  7. 7
    Sonstigeto give the crude product which
  8. 8
    Sonstigewas crystallized from ethyl acetate-hexanes

Vorschrift

To a solution of 3-(2,4-diphenylamino-pyrimidin-5-yl)-2-(3,5-dimethoxy-phenyl)-propionic acid methyl ester (0.11 mg, 0.23 mmol) (from Example 3c supra) in glacial acetic acid (2 mL) was added concentrated sulfuric acid (0.1 mL) in one portion. The reaction mixture was heated at 120° C. overnight. The reaction mixture was then diluted with ethyl acetate (50 mL) and quenched with 2 N aqueous sodium hydroxide solution. The organic layer was separated and successively washed with water (10 mL) and brine (10 mL), dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to give the crude product which was crystallized from ethyl acetate-hexanes to give 6-(3,5-dimethoxy-phenyl)-8-phenyl-2-phenylamino-5,8-dihydro-6H-pyrido[2,3-d]pyrimidin-7-one as light brown solid. (Yield 73.3 mg, 71.4%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07098332B2uspto-grants-2006_08