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

HRID 54340

반응식

HRID 54340 반응식
C(C[N:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[NH:8][C:7](=[O:15])[C:6]1=[O:16])(O)=O.[CH:17]1[C:22]([NH2:23])=[CH:21][CH:20]=[C:19](N)[CH:18]=1.[CH2:25]1CCC(N=C=NC2CCCCC2)CC1.C[N:41]([CH:43]=[O:44])C>>[C:17]1([CH3:25])[CH:18]=[CH:19][CH:20]=[CH:21][C:22]=1[NH:23][C:43]([NH:41][N:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[NH:8][C:7](=[O:15])[C:6]1=[O:16])=[O:44]

참가 물질

5

반응물 4

HCID 6228DimethylformamideHCID 7814P-PhenylenediamineHCID 10868DicyclohexylcarbodiimideHCID 129386642-(2,3-Dioxo-1,2,3,4-tetrahydroquinoxalin-1-yl)acetic acid

생성물 1

HCID 199585841-[[(o-Tolylamino)carbonyl]amino]-1,4-dihydro-2,3-quinoxalinedione

반응 조건

온도
28 °C

실험 절차

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: δ4.84 (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.

후처리

  1. filtrationThe precipitated solid was filtered
  2. additionthe clear filtrate was poured into water (10 mL)
  3. customThe solid thus obtained
  4. filtrationwas filtered
  5. dry with materialdried under vacuum (water aspirator)
  6. customto obtain 180 mg crude product as a brown powder
  7. customThe product was purified by Soxhlet extraction
  8. customat 120° C.
  9. waitfor 4 h
  10. customThe insoluble material (in the thimble) was dried under vacuum

출처 및 근거

ORD 기록
ord-303e98e6f5d64578824523a46575e45d
출처 데이터셋
uspto-grants-1997_04
특허 번호
US05622952

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