Phenyl isocyanate → 4-(6,7-Dimethoxy-4-quinazolinyl)-N-phenyl-1-piperazinecarboxamide

HRID 353126

Reaktionsgleichung

Reaktionsgleichung von HRID 353126
[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][N:7]=[C:6]2[N:15]1[CH2:20][CH2:19][NH:18][CH2:17][CH2:16]1.[C:21]1([N:27]=[C:28]=[O:29])[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>C(O)C>[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][N:7]=[C:6]2[N:15]1[CH2:16][CH2:17][N:18]([C:28]([NH:27][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[O:29])[CH2:19][CH2:20]1

Komponenten

4

Edukt 2

HCID 7672Phenyl isocyanateHCID 27584846,7-Dimethoxy-4-piperazin-1-yl-quinazoline

Produkt 1

HCID 110366394-(6,7-Dimethoxy-4-quinazolinyl)-N-phenyl-1-piperazinecarboxamideAusbeute 44,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

In 5 ml of ethanol was dissolved 278 mg (1.0 mmol) of 6,7-dimethoxy-4-piperazinylquinazoline obtained by the method described in South African Patent No. 67 06512 (1968), and 0.109 ml (1.0 mmol) of phenyl isocyanate was added thereto. The mixture was heated under reflux for 10 minutes and then allowed to cool to room temperature. The precipitated crystals were collected by filtration and recrystallized from ethanol to give 174.3 mg of the desired compound as colorless crystals. yield: 44%

Aufarbeitung

  1. customobtained by the method
  2. temperatureThe mixture was heated
  3. temperatureunder reflux for 10 minutes
  4. filtrationThe precipitated crystals were collected by filtration
  5. customrecrystallized from ethanol

Quellen und Nachweise

ORD-Eintrag
ord-5ffd5bb6f69f4aa7829f9648c102a026
Quelldatensatz
uspto-grants-2004_06
Patentnummer
US06750218B2

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