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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233147생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/233147

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
반응물4-(3-Bromopropoxy)-3-methoxybenzonitrileHCID 10423230—
용매AcetonitrileHCID 6342—
생성물4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxybenzonitrileHCID 1004711368.2%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591745
출처 데이터셋uspto-grants-1997_01
ORD IDord-9be2f0bd822547af82a2b49d45fb9e30
출처 메모uspto-grants-1997_01