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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2184489생성일: 2026년 10월 25일

Acetonitrile → 1-[4-[3-[4-(5-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanone

https://huagongshe.com/reaction/2184489

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Potassium CarbonateHCID 11430—
반응물5-Fluoro-3-(4-piperidinyl)-1,2-benzisoxazoleHCID 2794755—
반응물4-(3-Chloropropoxy)-3-methoxyacetophenoneHCID 7314264—
용매WaterHCID 962—
생성물1-[4-[3-[4-(5-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxyphenyl]ethanoneHCID 1032025293.8%

반응 단계

A mixture of 5-fluoro -3-(4-piperidinyl)-1,2-benzisoxazole (2.2 g, 10 mmol), 1-[4-(3-chloropropoxy)-3-methoxyphenyl]ethanone (2.4 g, 10 mmol). K2CO3 (1.4 g), a few crystals of Kl and acetonitrile (100 ml) was stirred and refluxed for 8 hours. The reaction was poured into water and the aqueous mixture was extracted with ethyl acetate. The ethyl acetate extract was washed (brine), dried (MgSO4), and concentrated to afford 4.0 g of a white solid. The solid was chromatographed on a Waters Prep 500 HPLC utilizing silica get columns and eluting with methylene chloride/methanol (5%). Concentration of the appropriate fractions afforded 2.0 g (47%) of 1-[4-[3-[4-(5-fluoro-1,2-benzisoxazol-3-yl)-1-methoxyphenyl]ethanone as a white crystalline solid, m.p.=103°-105° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE037729E1
출처 데이터셋uspto-grants-2002_06
ORD IDord-2eaac86dc63841d1bbf7b1a8c1c0f630
출처 메모uspto-grants-2002_06