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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 329047Erstellt: 24. Oktober 2026

Triethylamine → 2-Trifluoromethyl-10-[3-(4-beta-hydroxyethoxy-4-ethyl-piperidino)-propyl]-phenothiazine hydrochloride

https://huagongshe.com/de/reaction/329047

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt10-(3-Chloropropyl)-2-(trifluoromethyl)-10H-phenothiazineHCID 74294—
Edukt2-(4-Ethyl-4-piperidyloxy)-ethanolHCID 21440904—
LösungsmittelSodium IodideHCID 5238—
LösungsmittelMethyl Ethyl KetoneHCID 6569—
Produkt2-Trifluoromethyl-10-[3-(4-beta-hydroxyethoxy-4-ethyl-piperidino)-propyl]-phenothiazine hydrochlorideHCID 7063471847,6%

Reaktionsschritte

37.7 g of 10-(3-chloropropyl)-2-trifluoromethyl-phenothiazine were dissolved in 100 ml of methyl ethyl ketone and 16.5 g of sodium iodide, 11.1 g of triethylamine and then 19 g of 2-(4-ethyl-4-piperidyloxy)-ethanol dissolved in 100 ml of methyl ethyl ketone were successively added thereto. The mixture was refluxed for 20 hours and after cooling, the precipitate formed was removed by vacuum filtration. The filtrate was evaporated to dryness and the residue was dissolved in methylene chloride. The organic solution was washed with an aqueous solution of sodium bicarbonate, then with water, dried and concentrated to dryness. The residue was dissolved in an ethanol-ether mixture to which was added an ether solution of hydrogen chloride. The precipitate formed was recovered by vacuum filtration and was crystallized from isopropanol, then from acetonitrile to obtain 27 g of 2-trifluoromethyl-10-[3-(4-β-hydroxyethoxy-4-ethyl-piperidino)-propyl]-phenothiazine hydrochloride as white crystals, melting at 204° C and soluble in chloroform, water, dilute hydrochloride acid and methylene chloride.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04018922
Quelldatensatzuspto-grants-1977_04
ORD IDord-05916d27420145eebeb59d07122a90c9
Quellennotizuspto-grants-1977_04