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HRID 53711Erstellt: 23. Oktober 2026
Diethyl Oxalate → 5,7-Dichloro-1,4-dihydroquinoxaline-2,3-dione
https://huagongshe.com/de/reaction/53711
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diethyl Oxalate | HCID 7268 | — |
| Edukt | 3,5-Dichlorobenzene-1,2-diamine | HCID 4276835 | — |
| Produkt | 5,7-Dichloro-1,4-dihydroquinoxaline-2,3-dione | HCID 650260 | — |
Reaktionsschritte
The title compound (Leeson, P. D. et al., J. Med. Chem 34: 1243 (1991)) was prepared using an adaptation of the method of Cheeseman. (Cheeseman, G. W. H. J. Chem. Soc. 1171 (1962)). A mixture of diethyl oxalate (4.12 g, 28.2 mmol) and 3,5-dichloro-1,2-diaminobenzene (500 mg, 2.82 mmol) was heated to reflux under N2 for 6 h. The reaction was allowed to cool to room temperature and the pale yellow shiny solid collected by vacuum filtration and rinsed with EtOH (20 mL) and air dried to give 286 mg (44%). mp 326°-328° C. (dec) Lit 337°-340° C.). 1H NMR (d6 -DMSO) δ 7.05 (d, 1H, J=1.8, H-8), 7.32 (d, 1H, J=1.8, H-6), 11.5 (br s, 1H, NH), 12.1 (br s, 1H, NH). EIMS m/e 234 (M+4, 12), 232 (M+2, 67), 230 (M+, bp), 204 (52), 202 (77), 141 (19), 142 (59) EIHRMS calc. for C8H4Cl2N2O: 229.9650, found 229.9646.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05620979 |
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| Quelldatensatz | uspto-grants-1997_04 |
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| ORD ID | ord-ec8bc8f85f27423cb34524fc9ed7152e |
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| Quellennotiz | uspto-grants-1997_04 |
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