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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1792679Generated: November 3, 2026

Potassium Carbonate → N,N-dimethyl-4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxybenzamide

https://huagongshe.com/reaction/1792679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
ReactantN,N-dimethyl4 bromopropoxy-3-methoxybenzamideHCID 10358359—
SolventAcetonitrileHCID 6342—
ProductN,N-dimethyl-4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3-methoxybenzamideHCID 10049666—

Reaction Steps

A stirred mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzoisoxazole (3.9 g, 17.7 moles), N,N-dimethyl-4-bromopropoxy-3-methoxybenzamide (5.54 g, 17.5 mmoles) and K2CO3 (3 g) in acetonitrile (250 ml) was heated at reflux for one hour. At the end of the reaction, the insolubles were filtered and washed with dichloromethane. The solvent was removed on a rotary evaporator. The residue was purified by flash chromatography over a silica gel column. The product thus obtained as an oil weighted 7 . Crystallization from hot ethanol (45 ml) afforded analytically pure N,N-dimethyl-4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-propoxy]-3-methoxybenzamide, 3.95 g, 50%, as light yellow crystals, m.p.=126°-127° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039198E1
Source datasetuspto-grants-2006_07
ORD IDord-acbee8be9630420ebc838f58518b06d5
Source noteuspto-grants-2006_07