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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53753생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물AnilineHCID 6115—
반응물DimethylformamideHCID 6228—
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, 0.250 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620979
출처 데이터셋uspto-grants-1997_04
ORD IDord-f353e0c4d077491b84d0174268e2ebf0
출처 메모uspto-grants-1997_04