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HRID 53719Erstellt: 24. Oktober 2026

Diethyl Oxalate → 2,3-Dioxo-1,2,3,4-tetrahydroquinoxaline-6-carbonitrile

https://huagongshe.com/de/reaction/53719

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl OxalateHCID 7268—
Edukt3,4-DiaminobenzonitrileHCID 737285—
LösungsmittelAcetic AcidHCID 176—
Produkt2,3-Dioxo-1,2,3,4-tetrahydroquinoxaline-6-carbonitrileHCID 5100691—

Reaktionsschritte

The title compound was prepared using an adaptation of the method of Cheeseman. (Cheeseman, G. W. H. J. Chem. Soc. 1171 (1962)). A mixture of diethyl oxalate (3.90 g, 27.6 mmol) and 3,4-diaminobenzonitrile (275 mg, 2.06 mmol) was heated to reflux under N2 for 2 h. The reaction was allowed to cool to room temperature and the solid collected by vacuum filtration and rinsed with EtOH. The yellow brown solid was air dried to yield 156.6 mg (40.8%) which was >98% pure by 1H NMR. An analytically pure sample was prepared by recrystallization of 100 mg in 10 mL glacial acetic acid to give 21.2 mg of fine white crystals. 1H NMR (d6 -DMSO) δ 7.20 (d, J=8.1, 1H, ArH), 7.39 (d, J=1.2, 1H, ArH), 7.50 (dd, J=1.2, J=8.4, 1H, ArH), 12.09 (s, 1H, NH), 12.22 (s, 1H, NH). EIMS m/z 187(87, M+), 159 (100, bp), 131(83), 104 (77), 77 (65), 53 (43), 28 (30). EIHRMS calc. for C9H5N3O2 187.0381, found 187.0377.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05620979
Quelldatensatzuspto-grants-1997_04
ORD IDord-43a14b57f9c843fa86a1a55678f693ee
Quellennotizuspto-grants-1997_04