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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329049생성일: 2026년 10월 24일

Triethylamine → 2-Trifluoromethyl-10-[3-(4-heptyl-4-beta-hydroxy-ethoxy-piperidino)-beta-propyl]-phenothiazine hydrochloride

https://huagongshe.com/ko/reaction/329049

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물10-(3-Chloropropyl)-2-(trifluoromethyl)-10H-phenothiazineHCID 74294—
반응물2-(4-Heptyl-4-piperidyloxy)-ethanolHCID 21440901—
용매Sodium IodideHCID 5238—
용매Methyl Ethyl KetoneHCID 6569—
생성물2-Trifluoromethyl-10-[3-(4-heptyl-4-beta-hydroxy-ethoxy-piperidino)-beta-propyl]-phenothiazine hydrochlorideHCID 7063461332.4%

반응 단계

14.1 g of 2-trifluoromethyl-10-(3-chloropropyl)-phenothiazine were dissolved in 50 ml of methyl ethyl ketone and 6.14 g of sodium iodide, 4.15 g of triethylamine, then 10 g of 2-(4-heptyl-4-piperidyloxy)-ethanol dissolved in 50 ml of methyl ethyl ketone were successively added thereto. The mixture was refluxed with agitation for 40 hours and after cooling, the precipitate formed was removed by vacuum filtration. The organic solution was washed with an aqueous solution of sodium bicarbonate, then with water, dried and then concentrated. The said product was reacted with an ether solution of hydrogen chloride and the obtained precipitate was recovered by vacuum filtration and was crystallized from an ethanol ether mixture to obtain 7.8 g of 2-trifluoromethyl-10-[3-(4-heptyl-4-β-hydroxy-ethoxy-piperidino)-β-propyl]-phenothiazine hydrochloride as white crystals melting at 180° C and soluble in ethanol and insoluble in water and ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04018922
출처 데이터셋uspto-grants-1977_04
ORD IDord-2ac11dbfba764ba3a22b4f086f28994b
출처 메모uspto-grants-1977_04