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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329048생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/329048

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물10-(3-Chloropropyl)-2-(trifluoromethyl)-10H-phenothiazineHCID 74294—
반응물2-(4-Propyl-4-piperidyloxy)-ethanolHCID 21440879—
용매Sodium IodideHCID 5238—
용매Methyl Ethyl KetoneHCID 6569—
생성물2-Trifluoromethyl-10-[3-(4-beta-hydroxyethoxy-4-propylpiperidino)-propyl]-phenothiazineHCID 5426432799.6%

반응 단계

10 g of 2-trifluoromethyl-10-(3-chloropropyl)-phenothiazine were dissolved in 50 ml of methyl ethyl ketone and 4.36 g of sodium iodide, 2.9 g of triethylamine, then dropwise a solution of 5.4 g of 2-(4-propyl-4-piperidyloxy)-ethanol in 50 ml of methyl ethyl ketone were added successively thereto. The mixture was refluxed for 24 hours and after cooling, the precipitate formed was removed by vacuum filtration. The precipitate formed was removed by filtration and the filtrate was evaporated in vacuo and the residue was dissolved in methylene chloride. The organic solution was washed with an aqueous solution of sodium bicarbonate, then with water and the solution was dried and concentrated in vacuo to obtain 14.2 g of 2-trifluoromethyl-10-[3-(4-β-hydroxyethoxy-4-propylpiperidino)-propyl]-phenothiazine as a beige product which was dissolved in 50 ml of ethanol. The resulting solution was reacted with an ether solution of hydrogen chloride and the hydrochloride was precipitated by the addition of ether. The said precipitate was recovered by vacuum filtration and was washed with ether and crystallized from acetonitrile to obtain 7 g of 2-trifluoromethyl-10-[3-(4-β-hydroxyethoxy-4-propylpiperidino)-propyl]-phenothiazine hydrochloride as white crystals melting at 192° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04018922
출처 데이터셋uspto-grants-1977_04
ORD IDord-cb32354199474c3facec98c1d8c1246b
출처 메모uspto-grants-1977_04