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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211488Generated: October 30, 2026

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

https://huagongshe.com/reaction/2211488

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
Reactant1-[4-(3-Bromopropoxy)-3-methoxyphenyl]propanoneHCID 57102976—
SolventAcetonitrileHCID 6342—
Product1-[4-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl] propoxy]-3-methoxyphenyl]propanoneHCID 2196003331.8%

Reaction Steps

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2- benzisoxazole (2.8 g, 15.2 mmoles), K2CO3 (3 g), 1-[4-(3- bromopropoxy)-3-methoxyphenyl]propanone (4.6 g, 18.2 mmoles). in acetonitrile (100 ml) was heated at reflux for 2 hours. At the end of the reaction, the mixture was filtered and the solvent was concentrated and the residue was extracted into dichloromethane (300 ml). The dichloromethane was filtered and concentrate again. The crude material (6.4 g) was purified by flash chromatography over a silica gel column (SiO2, 50 g; eluted with dichloromethane, 700 ml; 1% methanol in dichloromethane, 1.4 1). The material thus purified (weight: 2.87 g, 51%) was recrystallized from ethanol (25 ml) to give 2.13 g of 1-[4-[3-[4-(6-fluoro-1,2- benzisoxazol-3-yl)-1-piperidinyl]propoxy]-3- methoxyphenyl]propanone as beige colored crystals, m.p.=118°-119° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039265E1
Source datasetuspto-grants-2006_09
ORD IDord-4b11aaf6bcc249d99cf3f56b59ea0226
Source noteuspto-grants-2006_09