Hydrochloric Acid → N-[6-chloro-5-(2-methoxyphenoxy)-2-(2-pyrimidinyl)-4-pyrimidinyl]-2-phenylethenesulfonamide

HRID 2287360Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2287360
[H-].[Na+].[C:3]1([CH:9]=[CH:10][S:11]([NH2:14])(=[O:13])=[O:12])[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[Cl:15][C:16]1[C:21]([O:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=2[O:29][CH3:30])=[C:20](Cl)[N:19]=[C:18]([C:32]2[N:37]=[CH:36][CH:35]=[CH:34][N:33]=2)[N:17]=1.Cl>CN(C)C=O>[Cl:15][C:16]1[N:17]=[C:18]([C:32]2[N:37]=[CH:36][CH:35]=[CH:34][N:33]=2)[N:19]=[C:20]([NH:14][S:11]([CH:10]=[CH:9][C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=2)(=[O:12])=[O:13])[C:21]=1[O:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=1[O:29][CH3:30]

Komponenten

6

Versuchsvorschrift

Sodium hydride (60%) (480 mg) was added to a solution of 1.00 g of 2-phenylethenesulfonamide in 10 ml of dimethylformamide with ice cooling followed by stirring at room temperature for 15 minutes. To this reaction solution was added 1.91 g of 4,6-dichloro-5-(2-methoxyphenoxy)-2-(2-pyrimidinyl)-pyrimidine with stirring. The reaction mixture was stirred at room temperature for 2.5 hours and poured into a mixture of 1N hydrochloric acid and ice. The resulting crystals were collected by filtration and pulverized in hot ethanol. After allowing to cool, the crystals were collected by filtration to give 1.91 g of N-[6-chloro-5-(2-methoxyphenoxy)-2-(2-pyrimidinyl)-4-pyrimidinyl]-2-phenylethenesulfonamide.

Aufarbeitung

  1. stirringwith stirring
  2. stirringThe reaction mixture was stirred at room temperature for 2.5 hours
  3. filtrationThe resulting crystals were collected by filtration
  4. temperatureto cool
  5. filtrationthe crystals were collected by filtration

Quellen und Nachweise

ORD-Eintrag
ord-e1e7b0678d6c4405a758250dd1da664a
Quelldatensatz
uspto-grants-2000_07
Patentnummer
US06083955

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