HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2249459Generated: October 29, 2026
2-(Ethylamino)ethanol → 4-Ethoxy-N-ethyl-N-(2-hydroxy-ethyl)-3-(5-ethyl-4-oxo-7-propyl-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-2-yl)benzenesulphonamide
https://huagongshe.com/reaction/2249459
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Ethylamino)ethanol | HCID 8072 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | HCID 135856749 | HCID 135856749 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Ethoxy-N-ethyl-N-(2-hydroxy-ethyl)-3-(5-ethyl-4-oxo-7-propyl-3,4-dihydroimidazo[5,1-f][1,2,4]triazin-2-yl)benzenesulphonamide | HCID 135856761 | 63.4% |
Reaction Steps
0.64 g (1.5 mmol) of 4-ethoxy-3-(5-ethyl-4-oxo-7-propyl-3,4-dihydro-imidazo[5,1-f][1,2,4]triazin-2-yl)-benzenesulphonyl chloride are dissolved in 20 ml of dichloromethane and cooled to 0° C. After addition of a spatula tip of dimethylaminopyridine, 0.40 g (4.50 mmol) of 2-(ethylamino)-ethanol are added, and the reaction mixture is stirred at room temperature overnight. The mixture is diluted with dichloromethane, the organic phase is washed with water and dried over sodium sulphate and the solvent is removed under reduced pressure. Chromatography (dichloromethane/methanol=95:5) gives 0.454 g (63%) of a colourless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07314871B2 |
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| Source dataset | uspto-grants-2008_01 |
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| ORD ID | ord-919007eccd4c482592c3b12ce79309ca |
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| Source note | uspto-grants-2008_01 |
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