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HRID 329049作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物10-(3-Chloropropyl)-2-(trifluoromethyl)-10H-phenothiazineHCID 74294—
反応物2-(4-Heptyl-4-piperidyloxy)-ethanolHCID 21440901—
溶媒Sodium IodideHCID 5238—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物2-Trifluoromethyl-10-[3-(4-heptyl-4-beta-hydroxy-ethoxy-piperidino)-beta-propyl]-phenothiazine hydrochlorideHCID 7063461332.4%

反応手順

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.

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-2ac11dbfba764ba3a22b4f086f28994b
出典メモuspto-grants-1977_04