HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → N-(2-Hydroxyethyl)-N'-[4-(5-oxo-4,5-dihydropyrazin-2-yl)phenyl]urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | 5-(4-Isocyanatophenyl)pyrazin-2(1H)-one | HCID 20208661 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-Hydroxyethyl)-N'-[4-(5-oxo-4,5-dihydropyrazin-2-yl)phenyl]urea | HCID 20208660 | — |
Reaction Steps
In a manner similar to Example 13b, 5-[4-(isocyanato)phenyl]-2(1H)-pyrazinone was reacted with 2-hydroxyethylamine (0.5 g) in dimethylformamide (5 ml) for 17 hours at room temperature. The mixture was purified by flash chromatography (chloroform--20% methanol/80% chloroform); the desired fractions were combined and evaporated under reduced pressure to affored a residue. This residue was washed with chloroform and dried to form the title compound; δ(DMSO-d6) 3.17 (sextet, 2H, --NHCH2), 3.47 (t, 2H, --CH2OH), 7.94, 8.06 (2d, J=1 Hz, pyrazinone H's).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04657906 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-cf32dd1fd0cf43fbaed21f17efb9e8f7 |
| Source note | uspto-grants-1987_04 |