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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl OxalateHCID 7268—
Edukt3,5-Dichlorobenzene-1,2-diamineHCID 4276835—
Produkt5,7-Dichloro-1,4-dihydroquinoxaline-2,3-dioneHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05620979
Quelldatensatzuspto-grants-1997_04
ORD IDord-ec8bc8f85f27423cb34524fc9ed7152e
Quellennotizuspto-grants-1997_04