Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Glyceraldehyde | HCID 751 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Edukt | HCID 178478620 | HCID 178478620 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | HCID 178521766 | HCID 178521766 | — |
Reaktionsschritte
To a solution of 6-piperazin-1-yl-2-(2-trifluoromethylphenylamino)-1H-benzimidazole-5-carboxylic acid (1H-indazol-6-yl)-amide trihydrochloride (0.2 mmol; see Example 88) in methanol (2 mL) was added glyceraldehyde (2 mmol), and the resulting mixture was stirred at RT for 60 min. The reaction mixture was then charged with solid sodium cyanoborohydride (1 mmol), and the stirring was continued at RT for 10h. The reaction mixture was then concentrated in vacuo, and the residue was suspended in water (10 mL) with vigorous stirring. After 30 min, the solid was filtered, washed with water, and dried under vacuum to afford 6-[4-(2-hydroxyethyl)-piperazin-1-yl]-2-(2-trifluoromethyl-phenylamino)-1H-benzimidazole-5-carboxylic acid (1H-indazol-6-yl)amide as a white solid. MS: m/z 565 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07820821B2 |
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| Quelldatensatz | uspto-grants-2010_10 |
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| ORD ID | ord-bc02f4da6c374bb89d661ef97cca3c1e |
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| Quellennotiz | uspto-grants-2010_10 |
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