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HRID 53753作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/53753

反応式

関与物質

役割名称HCID仕込み量
反応物AnilineHCID 6115—
反応物DimethylformamideHCID 6228—
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, 0.250 mmol) and aniline (25 mg, 0.25 mmol) in dry DMF (1.5 mL) under N2 at 28° C., DCC (55 mg, 0.25 mmol) was added in one portion. The solution was stirred at 28° C. for 18 h. The insoluble white solid was filtered and the clear filtrate was poured into water (6 mL). The precipitated solid was filtered and air dried to obtain 113 mg crude product as a grey powder. The crude product was then purified by Soxhlet extraction in boiling ethanol (20 mL), keeping the oil bath temperature at 120° C., for 5 h. The residue (in the thimble) was dried in the oven (approx. 70°-80° C.) overnight to furnish 35 mg pure (1H NMR) N-(N'-phenylcarboxamidyl)methyl-6,7-dibromo-1,4-dihydroquinox-aline-2,3-dione as a light grey powder; m.p. >300° C. (decomposes). 1H NMR: δ 4.97 (s, 1H), 6.99-7.11 (m, 1H), 7.23-7.37 (m, 2H), 7.44 (s, 1H), 7.52 (d, 2H, J=8.4 Hz), 7.73 (s, 1H), 10.25 (s, 1H), 12.25 (s, 1H). IR (KBr, cm-1): 3620, 3468, 1714, 1694, 1595, 1542. HRMS: Calculated for C16H11Br2N3O3, 450.9168; Observed, 450.9177.

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-f353e0c4d077491b84d0174268e2ebf0
出典メモuspto-grants-1997_04