Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 329045생성일: 2026년 10월 24일
Triethylamine → 2-Trifluoromethyl-10-[3-(4-beta-{2-methylheptanoyloxy}ethoxypiperidino)-propyl]-phenothiazine
https://huagongshe.com/ko/reaction/329045
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Flupimazine | HCID 218089 | — |
| 반응물 | 2-Methylheptanoyl chloride | HCID 14234519 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | 2-Trifluoromethyl-10-[3-(4-beta-{2-methylheptanoyloxy}ethoxypiperidino)-propyl]-phenothiazine | HCID 53721547 | 30% |
반응 단계
13.55 g of 2-trifluoromethyl-10-[3-(4-β-hydroxyethoxypiperidino)-propyl]-phenothiazine (prepared by Example XLIII), 5.4 ml of triethylamine and 100 ml of anhydrous benzene were added to a flask and a solution of 5.7 g of 2-methyl-heptanoic acid chloride in 50 ml of anhydrous benzene was added thereto. The mixture was agitated at room temperature for 24 hours and then the precipitate formed was removed by filtration. The benzene filtrate was washed with an aqueous solution of sodium bicarbonate, then with water. After drying and concentration of the benzene solution, the resulting oil was purified by chromatography on silica gel. After elution with ethanol and evaporation of the solvent, 5.2 g of 2-trifluoromethyl-10-[3-(4-β-{2-methylheptanoyloxy}ethoxypiperidino)-propyl]-phenothiazine as a clear oil were obtained.
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-f1c30b42051d48ec83d999ce52d27245 |
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| 출처 메모 | uspto-grants-1977_04 |
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