Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Edukt | 4-Nitroindazole | HCID 18057 | — |
| Edukt | Sodium Bisulfite | HCID 23665763 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 178526562 | HCID 178526562 | 84,8% |
Reaktionsschritte
A solution of 4-nitro-1H-indazole (50.0 g; 306 mmol) in N,N-dimethylformamide (600 mL) was cooled to 5° C. under a nitrogen atmosphere with stirring. Powdered potassium hydroxide (68.8 g; 1226 mmol) was added. A solution of iodine (156 g; 613 mmol) in DMF (200 mL) was added slowly to the reaction mixture over 2 hours maintaining the temperature between 5 and 10° C. The mixture was stirred at 25° C. for 24 hours. Additional iodine (39.0 g; 153.2 mmol) and potassium hydroxide (17.2 g; 306.5 mmol) was added. The mixture was stirred at 25° C. for a further 12 hours. The reaction mixture was added to an aqueous solution of sodium bisulfite (10% solution; 3300 mL) with stirring. The resulting precipitate was collected by filtration and washed with water. The material was dried in a vacuum oven at 40° C. The material was dissolved in methylene chloride/methanol (10:1; 1.5 L) and filtered through Celite® to remove inorganic impurities. Concentration of the solution under vacuum gave 3-iodo-4-nitro-1H-indazole as a yellow solid (75 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08841455B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-8fd7602e27f64a30b95606b1836bde8a |
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| Quellennotiz | uspto-grants-2014_09 |
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