4-Chloro-2-nitrophenyl isocyanate → N-(4-Chloro-2-nitrophenyl)-N'-{4-[(6,7-dimethoxy-4-quinolyl)oxy]phenyl}urea

HRID 1857253Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1857253
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[N:9]=[CH:8][CH:7]=[C:6]2[O:15][C:16]1[CH:21]=[CH:20][C:19]([NH2:22])=[CH:18][CH:17]=1.[Cl:23][C:24]1[CH:29]=[CH:28][C:27]([N:30]=[C:31]=[O:32])=[C:26]([N+:33]([O-:35])=[O:34])[CH:25]=1>C1(C)C=CC=CC=1>[Cl:23][C:24]1[CH:29]=[CH:28][C:27]([NH:30][C:31]([NH:22][C:19]2[CH:18]=[CH:17][C:16]([O:15][C:6]3[C:5]4[C:10](=[CH:11][C:12]([O:13][CH3:14])=[C:3]([O:2][CH3:1])[CH:4]=4)[N:9]=[CH:8][CH:7]=3)=[CH:21][CH:20]=2)=[O:32])=[C:26]([N+:33]([O-:35])=[O:34])[CH:25]=1

Komponenten

4

Versuchsvorschrift

6,7-Dimethoxy-4-(4-aminophenoxy)quinoline (123 mg) was dissolved in toluene (12 ml) with heat, 4-chloro-2-nitrophenyl isocyanate (172 mg) was added, and the admixture was refluxed with heat for 14 minutes. The separated crystals were filtered and then washed with toluene to obtain 174 mg of the title compound (yield: 85%).

Aufarbeitung

  1. temperaturewith heat
  2. temperaturethe admixture was refluxed
  3. temperaturewith heat for 14 minutes
  4. filtrationThe separated crystals were filtered
  5. washwashed with toluene

Quellen und Nachweise

ORD-Eintrag
ord-ecca966c00e14bdda99cd97484f9fd01
Quelldatensatz
uspto-grants-2000_11
Patentnummer
US06143764

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