Reaktionsgleichung
[NH2:1][C:2]1[CH:10]=[CH:9][C:5]2[N:6]=[CH:7][NH:8][C:4]=2[CH:3]=1.[F:11][C:12]1[C:19]([F:20])=[CH:18][C:17]([F:21])=[CH:16][C:13]=1[CH:14]=O.[Si]([C:26]#[N:27])(C)(C)C.Cl.[BH4-].[Na+].C([O:38][CH2:39]C)(OCC)OCC>>[NH:6]1[C:5]2[CH:9]=[CH:10][C:2]([N:1]3[CH:14]([C:13]4[CH:16]=[C:17]([F:21])[CH:18]=[C:19]([F:20])[C:12]=4[F:11])[C:39](=[O:38])[NH:27][CH2:26]3)=[CH:3][C:4]=2[N:8]=[CH:7]1Komponenten
7
Versuchsvorschrift
The compound was synthesized starting from 5-aminobenzimidazole (0.732 g, 5.5 mmol), 2,3,5-trifluorobenzaldehyde (0.57 mL, 5 mmol), TMSCN (0.625 mL, 5 mmol), concentrated aqueous HCl (15 mL), triethyl orthoformate (30 mL, excess), NaBH4 (0.157 g, 4.14 mmol) as described in method 4.
Aufarbeitung
- customThe compound was synthesized
Quellen und Nachweise
- ORD-Eintrag
- ord-e267de157ed245c98df1f1dc3ed94cdd
- Quelldatensatz
- uspto-grants-2013_07
- Patentnummer
- US08486940B2
Verknüpfte Notizen
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