HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 329405Erstellt: 24. Oktober 2026
Sodium Iodide → 4-(4-(4-(4-(3-Trifluoromethylphenyl)piperazinyl)butyl)-phenyl)-2-aminothiazole
https://huagongshe.com/de/reaction/329405
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | Sodium Carbonate | HCID 10340 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | TFMPP hydrochloride | HCID 3084246 | — |
| Edukt | 4-(4-(4-Chlorobutyl)phenyl)-2-aminothiazole hydrobromide | HCID 14211429 | — |
| Lösungsmittel | Methyl Isobutyl Ketone | HCID 7909 | — |
| Produkt | 4-(4-(4-(4-(3-Trifluoromethylphenyl)piperazinyl)butyl)-phenyl)-2-aminothiazole | HCID 14211430 | — |
Reaktionsschritte
To a 125 ml round-bottomed flask equipped with condenser and N2 inlet were added 2.61 g (7.5 mmol) of 4-(4-(4-chlorobutyl)phenyl)-2-aminothiazole hydrobromide, 2.0 g (7.5 mmol) of N-(3-trifluoromethylphenyl)piperazine hydrochloride, 2.62 ml (15.0 mmol) of diisopropylethylamine, 1.59 g (15.0 mmol) of sodium carbonate, 5 mg of sodium iodide, and 50 ml of methylisobutylketone. The reaction was heated at reflux for 3.5 days, cooled, and the precipitate filtered, and the filtrate evaporated. The residue was chromatographed on silica gel using methylene chloride/ethyl acetate and ethyl acetate as eluents. The product fractions were concentrated, taken up in methylene chloride/methanol, precipitated by addition of ethyl acetate saturated with hydrochloride, evaporated, and the residue triturated with ether/ethyl acetate to afford a white solid, m.p. 174°-179° C., 0.87 g (23%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04891375 |
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| Quelldatensatz | uspto-grants-1990_01 |
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| ORD ID | ord-b0d66922660d400b8d55e72f93b0914f |
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| Quellennotiz | uspto-grants-1990_01 |
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