Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49395Generated: October 27, 2026

Ethanolamine → 6-[4-(2-aminoethoxy)-phenyl]-4,5-dihydro-3(2H)-pyridazinone

https://huagongshe.com/reaction/49395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantWaterHCID 962—
Reactant6-(4-Fluorophenyl)-4,5-dihydro-3(2H)-pyridazinoneHCID 605878—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
Product6-[4-(2-aminoethoxy)-phenyl]-4,5-dihydro-3(2H)-pyridazinoneHCID 1444186634.4%

Reaction Conditions

Temperature65 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06706743B2
Source datasetuspto-grants-2004_03
ORD IDord-8ddbe8b1aadf48f8b8a28eaf3c5c5e12
Source noteuspto-grants-2004_03