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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53752생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/53752

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물P-PhenylenediamineHCID 7814—
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 acid N-carboxymethyl-1,4-dihydroquinoxaline-2,3-dione (200 mg, 0.910 mmol) and p-phenylenediamine (98 mg, 0.91 mmol) in DMF (2 mL) under N2 at 0° C., DCC (190 mg, 0.910 mmol) was added in one portion. The solution was allowed to warm to 28° C. and stirred at that temperature overnight. The precipitated solid was filtered and the clear filtrate was poured into water (10 mL). The solid thus obtained was filtered and dried under vacuum (water aspirator) to obtain 180 mg crude product as a brown 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 135 mg pure (1H NMR) N-(N'-(p-aminophenyl)carboxamidyl)methyl-1,4-dihydroquinoxaline-2,3-dione as a white powder. M.p. >300° C. (decomposes). 1H NMR: δ 4.84 (s, 2H), 4.93 (s,2H), 6.5 (d, 2H, J=8.4 Hz), 7.15-7.25 (m, 6H), 9.83 (s, 1H), 12.15 (s, 1H). IR (KBr, cm-1): 3462, 3143, 1793, 1693, 1593, 1443. HRMS: Calculated for C16H14N4O3, 310.1066; Observed, 310.1071.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620979
출처 데이터셋uspto-grants-1997_04
ORD IDord-fae12e89ba3a4d22aea0c38432ce4d1a
출처 메모uspto-grants-1997_04