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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233180생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/233180

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2,3-Dihydro-1,4-benzodioxin-2-ylmethyl methanesulfonateHCID 263445—
반응물3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
용매AcetonitrileHCID 6342—
생성물2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]methyl-1,4-benzodioxanHCID 15384968—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591745
출처 데이터셋uspto-grants-1997_01
ORD IDord-4da3560faa4d44f68695ad89466862f7
출처 메모uspto-grants-1997_01