戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 53719作成日:2026年10月25日

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

https://huagongshe.com/reaction/53719

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl OxalateHCID 7268—
反応物3,4-DiaminobenzonitrileHCID 737285—
溶媒Acetic AcidHCID 176—
生成物2,3-Dioxo-1,2,3,4-tetrahydroquinoxaline-6-carbonitrileHCID 5100691—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05620979
出典データセットuspto-grants-1997_04
ORD IDord-43a14b57f9c843fa86a1a55678f693ee
出典メモuspto-grants-1997_04