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HRID 265498作成日:2026年10月25日

Potassium Carbonate → 2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]methyl-1,4-benzodioxan

https://huagongshe.com/reaction/265498

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2,3-Dihydro-1,4-benzodioxin-2-ylmethyl methanesulfonateHCID 263445—
反応物3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
溶媒AcetonitrileHCID 6342—
生成物2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]methyl-1,4-benzodioxanHCID 15384968—

反応手順

A stirred mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (3.0 g, 13.6 mmol), K2CO3 (2.45 g, 17.7 mmol), 2-methanesulfonyloxymethyl-1,4-benzodioxan (3.35 g, 13.7 mmole) in acetonitrile (100 ml) was heated at reflux for 12 hours. At the end of the reaction, the insolubles were filtered and rinsed with dichloromethane. The organic solution was concentrated. The crude oil was purified by flash chromatography on a silica gel column. The fractions containing the pure product were pooled and concentrated to a light yellow oil (3.94 g, 74%). Crystallization from ethanol and petroleum ether gave 2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]methyl-1,4-benzodioxan as off-white crystals, 2.22 g, m.p.=86°-87° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05648363
出典データセットuspto-grants-1997_07
ORD IDord-5d1bd3cdccc74d369c0df6b376b36f32
出典メモuspto-grants-1997_07