Sodium hydride → 5-amino-1-(2-chlorobenzyl)-7-(trifluoromethyl)-1,3-dihydro-2H-benzimidazol-2-one
Reaktionsgleichung
[Cl:1][C:2]1[CH:26]=[CH:25][CH:24]=[CH:23][C:3]=1[CH2:4][N:5]([C:11]1[C:16]([C:17]([F:20])([F:19])[F:18])=[CH:15][C:14]([NH2:21])=[CH:13][C:12]=1[NH2:22])[C:6](=[O:10])OCC.[H-].[Na+].C(=O)(O)[O-].[Na+]>C(O)C>[NH2:21][C:14]1[CH:15]=[C:16]([C:17]([F:18])([F:20])[F:19])[C:11]2[N:5]([CH2:4][C:3]3[CH:23]=[CH:24][CH:25]=[CH:26][C:2]=3[Cl:1])[C:6](=[O:10])[NH:22][C:12]=2[CH:13]=1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Ethyl 2-chlorobenzyl[2,4-diamino-6-(trifluoromethyl)phenyl]carbamate (85.6 mg) was dissolved in ethanol (10 ml), and to the solution was added sodium hydride (17.7 mg). The reaction mixture was heated at reflux for 24 hours. After allowing to cool, to the reaction mixture was added saturated aqueous sodium bicarbonate solution, and the mixture was extracted 4 times with chloroform. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated in vacuo. The resultant residue was purified by preparative TLC (2 mm, 20×20 cm, CHCl3-methanol=5:1) to give the title compound (46.0 mg).
Aufarbeitung
- temperatureThe reaction mixture was heated
- temperatureat reflux for 24 hours
- temperatureto cool, to the reaction mixture
- extractionthe mixture was extracted 4 times with chloroform
- washThe organic layer was washed with saturated brine
- dry with materialdried over anhydrous sodium sulfate
- concentrationconcentrated in vacuo
- customThe resultant residue was purified by preparative TLC (2 mm, 20×20 cm, CHCl3-methanol=5:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-5f92d9fbca3e4bc7aa638c6258538e88
- Quelldatensatz
- uspto-grants-2005_09
- Patentnummer
- US06939887B2
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