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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53750생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/53750

반응식

참여 물질

역할이름HCID투입량
반응물AnilineHCID 6115—
반응물DimethylformamideHCID 6228—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물2-(2,3-Dioxo-1,2,3,4-tetrahydroquinoxalin-1-yl)acetic acidHCID 12938664—
생성물1-[[(o-Tolylamino)carbonyl]amino]-1,4-dihydro-2,3-quinoxalinedioneHCID 19958584—

반응 조건

온도28 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620979
출처 데이터셋uspto-grants-1997_04
ORD IDord-ab2997d5f3a743cf9955ce38dffdac4b
출처 메모uspto-grants-1997_04