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HRID 53750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/53750

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 1-carboxymethyl-1,4-dihydroquinoxaline-2,3-dione (100 mg, 0.450 mmol) and aniline (62 mg, 0.66 mmol) in dry DMF (2 mL) under N2 at 28° C., DCC (95 mg, 0.46 mmol, Aldrich) 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 poured into water (30 mL). The solid thus obtained was filtered and dried under vacuum (water aspirator) to yield 133 mg crude product as a grey powder. It 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 55 mg of pure (1H NMR) N-(N'-phenylcarboxamidyl)methyl-1,4-dihydroquinoxaline-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 the pure product). M.p. >300° C. (decomposes). 1H NMR: δ 4.92 (s, 2H), 7.01-7.30 (m, 7H), 7.51 (d, 2H, J=6.9 Hz), 10.26 (s, 1H), 12.13 (s, 1H). IR (KBr, cm-1): 3148, 1715, 1671, 1600, 1557. HRMS: Calculated for C16H3N3O3, 295.0951; Observed, 296.1033.

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-ab2997d5f3a743cf9955ce38dffdac4b
出典メモuspto-grants-1997_04