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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329047생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/329047

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물10-(3-Chloropropyl)-2-(trifluoromethyl)-10H-phenothiazineHCID 74294—
반응물2-(4-Ethyl-4-piperidyloxy)-ethanolHCID 21440904—
용매Sodium IodideHCID 5238—
용매Methyl Ethyl KetoneHCID 6569—
생성물2-Trifluoromethyl-10-[3-(4-beta-hydroxyethoxy-4-ethyl-piperidino)-propyl]-phenothiazine hydrochlorideHCID 7063471847.6%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04018922
출처 데이터셋uspto-grants-1977_04
ORD IDord-05916d27420145eebeb59d07122a90c9
출처 메모uspto-grants-1977_04