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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329037생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/329037

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물TriethylamineHCID 8471—
반응물10-(3-Chloropropyl)-2-(trifluoromethyl)-10H-phenothiazineHCID 74294—
반응물2-(Piperidin-4-yloxy)ethan-1-olHCID 20295332—
용매Methyl Ethyl KetoneHCID 6569—
생성물Ethanol, 2-((1-(3-(2-(trifluoromethyl)-10H-phenothiazin-10-yl)propyl)-4-piperidinyl)oxy)-, hydrochloride (1:1)HCID 21808871%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04018922
출처 데이터셋uspto-grants-1977_04
ORD IDord-889f9245fe624fdbbb11d67bcb861e23
출처 메모uspto-grants-1977_04