Reaktionsgleichung
[N:1]1([CH2:6][CH2:7][CH2:8][NH2:9])[CH:5]=[CH:4][N:3]=[CH:2]1.[OH:10][C:11]1[CH:12]=[CH:13][CH:14]=[C:15]2[C:20]=1[N:19]=[C:18]([CH:21]=O)[CH:17]=[CH:16]2.C[Si]([N:27]=[N+:28]=[N-:29])(C)C.[N+:30]([CH2:32][C:33]([CH3:36])([CH3:35])[CH3:34])#[C-:31]>CO>[CH3:34][C:33]([CH3:36])([CH3:35])[CH2:32][N:30]1[C:31]([CH:21]([NH:9][CH2:8][CH2:7][CH2:6][N:1]2[CH:5]=[CH:4][N:3]=[CH:2]2)[C:18]2[CH:17]=[CH:16][C:15]3[C:20](=[C:11]([OH:10])[CH:12]=[CH:13][CH:14]=3)[N:19]=2)=[N:29][N:28]=[N:27]1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
3-Imidazol-1-yl-propylamine (1 mmol) and 8-Hydroxy-quinoline-2-carbaldehyde (1 mmol) were combined in methanol (2 ml, dry). After 2 hours Trimethylsilylazide (5 mmol) and 1-Isocyano-2,2-dimethyl-propane (1 mmol) was added. The reaction was stirred at room temperature for 48 h. After evaporation of the solvent the residue was purified with chromatographic methods.
Aufarbeitung
- customAfter evaporation of the solvent the residue
- customwas purified with chromatographic methods
Quellen und Nachweise
- ORD-Eintrag
- ord-3470187e804f4bbabac598a8116168a6
- Quelldatensatz
- uspto-grants-2010_06
- Patentnummer
- US07741354B2
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