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HRID 329038作成日:2026年10月26日

Sodium Iodide → 2-Butanol, 3-((1-(3-(2-(trifluoromethyl)-10H-phenothiazin-10-yl)propyl)-4-piperidinyl)oxy)-

https://huagongshe.com/reaction/329038

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物TriethylamineHCID 8471—
反応物10-(3-Chloropropyl)-2-(trifluoromethyl)-10H-phenothiazineHCID 74294—
反応物1,2-Dimethyl-2-(4-piperidyloxy)-ethanolHCID 21440907—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物2-Butanol, 3-((1-(3-(2-(trifluoromethyl)-10H-phenothiazin-10-yl)propyl)-4-piperidinyl)oxy)-HCID 21809348%

反応手順

22.5 g (0.15 mole) of sodium iodide were added to a solution of 51.5 g (0.15 mole) of 10-(3-chloropropyl)-2-trifluoromethyl-phenothiazine in 400 ml of methyl ethyl ketone followed by the addition of 15.2 g (0.15 mole) of triethylamine and then 26 g (0.15 mole) of 1,2-dimethyl-2-(4-piperidyloxy)-ethanol. The mixture was then refluxed for 20 hours and after cooling, the precipitate formed was removed by vacuum filtration. The filtrate was evaporated to dryness and the oil residue was chromatographed over 1 kg of neutral alumina. Elution with ethyl acetate gave 34.5 g (48% yield) of 2-trifluoromethyl-10-[3-(4-[1,2-dimethyl-2-hydroxyethoxy]-piperidino)-propyl]-phenothiazine in the form of a clear amber oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04018922
出典データセットuspto-grants-1977_04
ORD IDord-e8008bdff8df4e0796e205ef0c9844a3
出典メモuspto-grants-1977_04