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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53754생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/53754

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물3-NitroanilineHCID 7423—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-Carboxymethyl-6,7-dibromo-1,4-dihydroquinoxaline-2,3-dioneHCID 19958556—
생성물1-[[(o-Tolylamino)carbonyl]amino]-1,4-dihydro-2,3-quinoxalinedioneHCID 19958584—

반응 조건

온도28 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620979
출처 데이터셋uspto-grants-1997_04
ORD IDord-a1b0218abebe4c8cacff79bbf9fe808c
출처 메모uspto-grants-1997_04