돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 55572생성일: 2026년 10월 26일

Dimethylformamide → 1-[4-[4-[4-(6-Fluoro1,2-benzisoxazol-3-yl)-1-piperidinyl]butoxy]-3-methoxyphenyl]ethanone

https://huagongshe.com/reaction/55572

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Potassium CarbonateHCID 11430—
반응물R-56109 hydrochlorideHCID 11334359—
반응물1-[4-(4-Bromobutoxy)3-methoxyphenyl]ethanoneHCID 14407171—
용매WaterHCID 962—
생성물1-[4-[4-[4-(6-Fluoro1,2-benzisoxazol-3-yl)-1-piperidinyl]butoxy]-3-methoxyphenyl]ethanoneHCID 1009479087.4%

반응 조건

온도75 °C

반응 단계

A stirred mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole hydrochloride (5.1 g, 0.02 mol), K2CO3 (5.2 g, 0.04 mol), 1-[4-(4-bromobutoxy)-3-methoxyphenyl]ethanone (6.6 g,: 22 mmol), and dimethylformamide (60 ml) was heated at 75° C. for 5 hours. The reaction was poured into water, and the aqueous mixture was extracted with ethyl acetate. The ethyl acetate was washed (water), dried (MgSO4), and the solvent was concentrated to yield initially an oil, which solidified upon standing. The solid was triturated with hexane and collected to afford 7.7 g of the product as a waxy solid. The compound was chromatographed on a Waters Prep 500 utilizing silica gel columns and eluting with dichloromethane/methanol (5%). Concentration of the appropriate fractions yielded 5.1 g of off-white solid 1-[4-[4-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-butoxy]-3-methoxyphenyl]ethanone, which when recrystallized from ethyl alcohol yielded 3.2 g (36%) of feathery-white needles, m.p.=88°-90° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05624927
출처 데이터셋uspto-grants-1997_04
ORD IDord-a6f77f6c15ed49f49233038e896d6b3c
출처 메모uspto-grants-1997_04