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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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물FlupimazineHCID 218089—
반응물2-Methylheptanoyl chlorideHCID 14234519—
용매BenzeneHCID 241—
생성물2-Trifluoromethyl-10-[3-(4-beta-{2-methylheptanoyloxy}ethoxypiperidino)-propyl]-phenothiazineHCID 5372154730%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04018922
출처 데이터셋uspto-grants-1977_04
ORD IDord-f1c30b42051d48ec83d999ce52d27245
출처 메모uspto-grants-1977_04