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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 10-(3-Chloropropyl)-2-(trifluoromethyl)-10H-phenothiazine | HCID 74294 | — |
| 반응물 | 2-(4-Ethyl-4-piperidyloxy)-ethanol | HCID 21440904 | — |
| 용매 | Sodium Iodide | HCID 5238 | — |
| 용매 | Methyl Ethyl Ketone | HCID 6569 | — |
| 생성물 | 2-Trifluoromethyl-10-[3-(4-beta-hydroxyethoxy-4-ethyl-piperidino)-propyl]-phenothiazine hydrochloride | HCID 70634718 | 47.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04018922 |
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| 출처 데이터셋 | uspto-grants-1977_04 |
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| ORD ID | ord-05916d27420145eebeb59d07122a90c9 |
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| 출처 메모 | uspto-grants-1977_04 |
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