Reaktion #11867
ord-71202caef48949bf8ff4e43739e43746
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Sonstigequenched with 2 N aqueous sodium hydroxide solution
- 2SonstigeThe organic layer was separated
- 3Waschensuccessively washed with water (10 mL) and brine (10 mL)
- 4Trocknendried over anhydrous sodium sulfate
- 5Filtrationfiltered
- 6Einengenconcentrated in vacuo
- 7Sonstigeto give the crude product which
- 8Sonstigewas 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%).