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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktSodium CarbonateHCID 10340—
EduktDiisopropylethylamineHCID 81531—
EduktTFMPP hydrochlorideHCID 3084246—
Edukt4-(4-(4-Chlorobutyl)phenyl)-2-aminothiazole hydrobromideHCID 14211429—
LösungsmittelMethyl Isobutyl KetoneHCID 7909—
Produkt4-(4-(4-(4-(3-Trifluoromethylphenyl)piperazinyl)butyl)-phenyl)-2-aminothiazoleHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04891375
Quelldatensatzuspto-grants-1990_01
ORD IDord-b0d66922660d400b8d55e72f93b0914f
Quellennotizuspto-grants-1990_01