Reaktion #77673

Reaktionsgleichung

Water

potassium tert-butoxide

ethanolamine

6-(4-fluorophenyl)-4,5-dihydro-2H-pyridazine-3-one

→

product

Ausbeute 34.4%

6-[4(2-Amino-ethoxy)-phenyl]-4,5-dihydro-2H-pyridazin-3-one

Ausbeute 34.4%

Lösungsmittel

dimethylsulfoxide

Reaktionsbedingungen

Aufarbeitung

1. 1
   TemperaturThis dark-colored solution was heated to about 80° C. for about twelve hours
2. 2
   Temperaturwas then cooled to room temperature
3. 3
   Sonstigethe resulting tan solid was removed by filtration
4. 4
   SonstigeThis crude solid was then purified by column chromatography (silica gel; 5% methanol/dichloromethane to 15% methanol/dichloromethane)

Vorschrift

In a flame-dried, round-bottomed flask, ethanolamine (1.7 ml, 28.1 mmol) was dissolved in dimethylsulfoxide (9.5 ml), and potassium tert-butoxide (95%, 3.3 g, 28.1 mmol) was added to the solution. This mixture was stirred at about 65° C. for about ten minutes, and then 6-(4-fluorophenyl)-4,5-dihydro-2H-pyridazine-3-one (3.6 g, 18.7 mmol) was added. This dark-colored solution was heated to about 80° C. for about twelve hours, and was then cooled to room temperature. Water was added, and the resulting tan solid was removed by filtration. This crude solid was then purified by column chromatography (silica gel; 5% methanol/dichloromethane to 15% methanol/dichloromethane) to afford the product as a white solid (1.5 g, 34% yield). LRMS ([M+H]+)=234.2.

Quelle