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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 6-(4-Fluorophenyl)-4,5-dihydro-3(2H)-pyridazinone | HCID 605878 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 6-[4-(2-aminoethoxy)-phenyl]-4,5-dihydro-3(2H)-pyridazinone | HCID 14441866 | 34.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06706743B2 |
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| Source dataset | uspto-grants-2004_03 |
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| ORD ID | ord-8ddbe8b1aadf48f8b8a28eaf3c5c5e12 |
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| Source note | uspto-grants-2004_03 |
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