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HRID 1734090作成日:2026年10月25日

Potassium Iodide → 6-Acetyl-3-ethyl-2-(2-(4-(6-fluorobenzo-(b)thiophen-3-yl)piperidin-1-yl)ethyl)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine hydrochloride

https://huagongshe.com/reaction/1734090

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物6-Acetyl-2-(2-chloroethyl)-3-ethyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridineHCID 21472043—
反応物4-(6-Fluorobenzo(b)thiophen-3-yl)piperidine hydrochlorideHCID 22649334—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
生成物6-Acetyl-3-ethyl-2-(2-(4-(6-fluorobenzo-(b)thiophen-3-yl)piperidin-1-yl)ethyl)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine hydrochlorideHCID 2147194634.5%

反応条件

温度70 °C

反応手順

A mixture of 0.7 g of 6-acetyl-2-(2-chloroethyl)-3-ethyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine, 0.7 g of 4-(6-fluorobenzo(b)thiophen-3-yl)piperidine hydrochloride, 1.8 g of potassium carbonate and 0.6 g of potassium iodide in 25 ml of dimethylformamide and 25 ml of toluene was stirred at 70° C. for 7 hours and poured into water. The toluene layer was washed with water, dried over magnesium and concentrated. The residue was purified by column chromatography on a silica gel and dissolved in ethanol to convert hydrochloride thereof, and then recrystallized from methanol to give 0.45 g of 6-acetyl-3-ethyl-2-(2-(4-(6-fluorobenzo-(b)thiophen-3-yl)piperidin-1-yl)ethyl)-4,5,6,7-tetrahydrothieno[2,3-c]pyridine hydrochloride, m.p. 240° C. (decomposition).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05532240
出典データセットuspto-grants-1996_07
ORD IDord-61311feb51e642fcb40ffd919e0b24b2
出典メモuspto-grants-1996_07