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HRID 357345作成日:2026年10月25日

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

https://huagongshe.com/reaction/357345

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3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
反応物4-(3-Bromopropoxy)-3-methoxybenzonitrileHCID 10423230—
溶媒AcetonitrileHCID 6342—
生成物4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxybenzonitrileHCID 1004711368.2%

反応手順

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (3.0 g, 13.6 mmol), K2CO3 (2.8 g), 4-(3-bromopropoxy)-3-methoxybenzonitrile (4.0 g, 14.8 mmol) in acetonitrile (70 ml) was heated at reflux for 3 hours. At the end of the reaction, the solvent was removed on a rotary evaporator. The organic material was extracted into dichloromethane (250 ml) and the inorganics were filtered off. The dichloromethane solution was concentrated to a crude oil. The purification was done by flash chromatography over a silica gel column (SiO2, 55 g; eluted with dichloromethane, 600 ml; 1% methanol in dichloromethane, 600 ml). The material thus obtained was crystallized from a small amount of dichloromethane. Recrystallization from ethanol (25 ml) provided 3.8 g (68%) of 4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-propoxy]-3-methoxybenzonitrile as white crystals, m.p.=107°-108° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05840727
出典データセットuspto-grants-1998_11
ORD IDord-6f1d2e97cb9b4ac897bfc77b3d5e7d4c
出典メモuspto-grants-1998_11