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HRID 53751作成日:2026年10月23日

Dimethylformamide → 1-[[(o-Tolylamino)carbonyl]amino]-1,4-dihydro-2,3-quinoxalinedione

https://huagongshe.com/ja/reaction/53751

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物4-NitroanilineHCID 7475—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物2-(2,3-Dioxo-1,2,3,4-tetrahydroquinoxalin-1-yl)acetic acidHCID 12938664—
生成物1-[[(o-Tolylamino)carbonyl]amino]-1,4-dihydro-2,3-quinoxalinedioneHCID 19958584—

反応条件

温度28 °C

反応手順

To a stirred solution of N-carboxymethyl-1,4-dihydroquinoxaline-2,3-dione (250 mg, 1.140 mmol) and p-nitroaniline (156 mg, 1.140 mmol) in DMF (3 mL) under N2 at 0° C., DCC (233 mg, 1.140 mmol) was added in one portion. The solution was allowed to warm to 28° C. and stirred at that temperature overnight. The precipitated solid was filtered and the clear filtrate was poured into water (30 mL). The solid thus obtained was filtered and dried under vacuum (water aspirator) to obtain 100 mg crude product as a yellow powder. The crude product was purified by Soxhlet extraction in boiling ethanol (20 mL), keeping the oil bath temperature at 120° C., for 4 h. The insoluble material (in the thimble) was dried under vacuum to obtain 23 mg pure (1H NMR) N-(N'-(p-nitrophenyl)carboxamidyl)methyl-1,4-dihydroquinoxaline-2,3-dione as a light yellow powder (some of the product also ends up being extracted by hot ethanol which accounts for the low yield of the pure product). M.p. >300° C. (decomposes). 1H NMR: δ 5.02 (s, 1H), 7.13-7.3 (m, 4H), 7.78 (d, 1H, J=8.4 Hz), 8.21 (d, 1H, J=8.4 Hz), 10.92 (s, 1H), 12.16 (s, 1H). IR (KBr, cm-1): 3453, 1701, 1684, 1625, 1572, 1509. HRMS: Calculated for C16H12N4O5, 340.0808; Observed, 340.0811.

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-6f1926f06f3d458fadcdb003b53121f4
出典メモuspto-grants-1997_04