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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 329037Erstellt: 24. Oktober 2026

Sodium Iodide → Ethanol, 2-((1-(3-(2-(trifluoromethyl)-10H-phenothiazin-10-yl)propyl)-4-piperidinyl)oxy)-, hydrochloride (1:1)

https://huagongshe.com/de/reaction/329037

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktTriethylamineHCID 8471—
Edukt10-(3-Chloropropyl)-2-(trifluoromethyl)-10H-phenothiazineHCID 74294—
Edukt2-(Piperidin-4-yloxy)ethan-1-olHCID 20295332—
LösungsmittelMethyl Ethyl KetoneHCID 6569—
ProduktEthanol, 2-((1-(3-(2-(trifluoromethyl)-10H-phenothiazin-10-yl)propyl)-4-piperidinyl)oxy)-, hydrochloride (1:1)HCID 21808871%

Reaktionsschritte

17.6 g (0.117 mole) of sodium iodide were added to a solution of 40 g (0.17 mole) of 10-(3-chloropropyl)-2-trifluoromethyl-phenothiazine in 350 ml of methyl ethyl ketone followed by the addition of first 11.8 g (0.117 mole) of triethylamine and then 17 g (0.117 mole) of 2-(4-piperidyloxy)-ethanol. The resulting solution was refluxed for 20 hours and after cooling, the precipitate was removed by vacuum filtration. The filtrate was evaporated to dryness. The oil residue was stirred with a mixture of ether and dilute hydrochloric acid and the precipitate formed was recovered by vacuum filtration and crystallized from a 95% ethanol-ether mixture to obtain 40.5 g (71% yield) of 10-[3-(4-β-hydroxyethoxypiperidino) propyl]-2-trifluoromethyl-phenothiazine hydrochloride in the form of white crystals melting at 218°-219° C on a heated microscopic stage.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04018922
Quelldatensatzuspto-grants-1977_04
ORD IDord-889f9245fe624fdbbb11d67bcb861e23
Quellennotizuspto-grants-1977_04