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HRID 53754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/53754

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物3-NitroanilineHCID 7423—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物1-Carboxymethyl-6,7-dibromo-1,4-dihydroquinoxaline-2,3-dioneHCID 19958556—
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-6,7-dibromo-1,4-dihydroquinoxaline-2,3-dione (100 mg, 0.260 mmol) and m-nitroaniline (40 mg, 0.29 mmol) in dry DMF (2 mL) under N2 at 28° C., DCC (60 mg, 0.29 mmol) was added in one portion. The solution was stirred for 4 h at 28° C. The insoluble solid was filtered and washed with DMF (1 mL). The clear filtrate was then poured into water (30 mL). The precipitated solid was filtered and dried under vacuum (water aspirator) to obtain 65 mg crude product as a yellow powder. The 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 30 mg pure (1H NMR) N-(N'-(m-nitrophenyl)carboxamidyl)-methyl-6,7-dibromo-1,4-dihydroquinox-aline-2,3-dione as a white solid (some of the product also ends up being extracted by hot ethanol which accounts for the low yield of pure product). M.p. >300° C. (decomposes). 1H NMR: δ 4.98 (s, 1H), 7.45 (s, 1H), 7.61 (d of d seen as at, J=8.1Hz) 7.79(s, 1H), 7.86 (d, 1H, J=9 Hz), 7.91 (d, 1H, J=8.4 Hz), 8.54 (s, 1H), 10.76 (s, 1H), 12.28 (s, 1H). IR (KBr, cm4): 3444, 3289, 1707, 1686, 1672, 1602. HRMS: Calculated for C16H10Br2N4O5, 495.9018; Observed, 495.9008.

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-a1b0218abebe4c8cacff79bbf9fe808c
出典メモuspto-grants-1997_04