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HRID 55578作成日:2026年10月27日

Potassium Carbonate → 1-[2-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)1-piperidinyl]propoxy]-5-methylphenyl]ethanone

https://huagongshe.com/reaction/55578

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1-[2-(3-Bromopropoxy)-5-methylphenyl]ethanoneHCID 10423299—
反応物R-56109 hydrochlorideHCID 11334359—
溶媒DimethylformamideHCID 6228—
溶媒AcetonitrileHCID 6342—
生成物1-[2-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)1-piperidinyl]propoxy]-5-methylphenyl]ethanoneHCID 1047668146.2%

反応条件

温度95 °C

反応手順

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole hydrochloride (2.87 g, 11.23 mmol), K2CO3 (2.5 g), 1-[2-(3-bromopropoxy)-5-methylphenyl]ethanone (3.74 g, 13.8 mmol) in dimethylformamide (10 ml) and acetonitrile (.50 ml) was heated at 95° C. for 6 hours. At the end of the reaction, the solvent was concentrated and the mixture was extracted into dichloromethane (300 ml). The organic solution was washed with water and brine, dried over MgSO4, then concentrated down to a crude oil. The purification was done by flash chromatography over a silica gel column (SiO2, 60 g, eluted with 1% CH3OH:dichloromethane: 1.2 l; 3% CH3OH:dichloromethane: 600 ml). The material thus obtained was crystallized from a small volume of ether and hexane to provide 2.13 g (46%) of off-white 1-[2-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-5-methylphenyl]ethanone, m.p.=92°-93° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624927
出典データセットuspto-grants-1997_04
ORD IDord-ee1fee9fa2914c37889ebdbe2e9175a4
出典メモuspto-grants-1997_04