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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744421Generated: October 28, 2026

3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazole → 4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-2-hydroxy-1-propoxy]-3-methoxyphenyl methanone

https://huagongshe.com/reaction/744421

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
Reactant3-Methoxy-4-(2-oxiranylmethoxy)benzaldehydeHCID 11344798—
SolventIsopropanolHCID 3776—
Product4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-2-hydroxy-1-propoxy]-3-methoxyphenyl methanoneHCID 1846736889.2%

Reaction Conditions

Temperature55 °C

Reaction Steps

A stirred mixture of 4-(2,3-epoxypropoxy)-3-methoxyphenyl methanone (4.5 g, 22.5 mmol) and 4-(6-fluoro-1,2-benzisoxazol-3-yl)piperidine (5.36 g, 24.3 retool) in isopropyl alcohol (150 ml) was heated at 55° C. for 16 hours. The mixture was cooled and the solvent was removed on a rotary evaporator. The residue was purified by flash chromatography over a silica gel column (SiO2, 80 g; eluted with dichloromethane, DCM, and 1% CH3OH in DCM). The oil thus obtained solidified quickly, weight: 9.47 g. Recrystallization from ethanol and isopropyl ether, then toluene provided 8.6 g (86%) of white crystals, m.p.=107°-108° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559117
Source datasetuspto-grants-1996_09
ORD IDord-6b35a197b26e44d8b9752d5c0fd7ac66
Source noteuspto-grants-1996_09