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HRID 233833作成日:2026年10月25日

Potassium Carbonate → 1-[4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3methylphenyl]ethanone hemifumarate

https://huagongshe.com/reaction/233833

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Fumaric AcidHCID 444972—
反応物1-[4-(3-Bromopropoxy)-3-methylphenyl]ethanoneHCID 9993319—
反応物R-56109 hydrochlorideHCID 11334359—
溶媒EthanolHCID 702—
溶媒DimethylformamideHCID 6228—
溶媒AcetonitrileHCID 6342—
生成物1-[4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3methylphenyl]ethanone hemifumarateHCID 131718779—

反応条件

温度95 °C

反応手順

A stirred mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole hydrochloride (3.0 g; 11.7 mmol), K2CO3 (3.0 g), and 1-[4-(3-bromopropoxy)-3-methylphenyl]ethanone (3.19 g) in dimethylformamide (20 ml) and acetonitrile (50 ml) was heated at 95° C. for 4 hours. At the end of the reaction, the solvent was concentrated down to about 30 ml, then partitioned between water (200 ml) and dichloromethane (300 ml). The dichloromethane solution was separated and washed with water and brine, then dried over MgSO4. The crude product from the evaporated solution was purified by flash chromatography over a silica gel column (SiO2, 60 g, eluted with 1% methanol in dichloromethane, 600 ml; 2% methanol in dichloromethane, 600 ml). The material thus obtained was a light yellow oil, weight: 2.07 g (43%). This oil was dissolved in ethanol and treated with a solution of fumaric acid (585 mg) in ethanol. The 1-[4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methylphenyl]-ethanone hemifumarate crystals formed on cooling at 0° C. This was collected and weighed 1.5 g, m.p.=185°-187° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05593995
出典データセットuspto-grants-1997_01
ORD IDord-9148b7f3e71e413499835376a9ee763f
出典メモuspto-grants-1997_01