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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781652Generated: October 30, 2026

Potassium Carbonate → 1-[2-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)1-piperidinyl]propoxy]-5-methylphenyl]ethanone

https://huagongshe.com/reaction/1781652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-[2-(3-Bromopropoxy)-5-methylphenyl]ethanoneHCID 10423299—
ReactantR-56109 hydrochlorideHCID 11334359—
SolventDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
Product1-[2-[3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)1-piperidinyl]propoxy]-5-methylphenyl]ethanoneHCID 1047668146.2%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole hydrochloride (2.87 g, 11.23 mmol), K2CO3 (2.5 g), 1-[2-(3-bromopropoxy)-5-methylphenyl]ethanone (3.74 g, 13.8 mmol) in dimethylformamide (10 ml) and acetonitrile (50 ml) was heated at 95° C. for 6 hours. At the end of the reaction, the solvent was concentrated and the mixture was extracted into dichloromethane (300 ml). The organic solution was washed with water and brine, dried over MgSO4 then concentrated down to a crude oil. The purification was done by flash chromatography over a silica gel column (SiO2, 60 g, eluted with 1% CH3OH:dichloromethane: 1.2 l; 3% CH3OH:dichloromethane: 600 ml). The material thus obtained was crystallized from a small volume of ether and hexane to provide 2.13 g (46%) of off-white 1-[2-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]propoxy]-5-methylphenyl]ethanone, m.p.=92°-93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05633265
Source datasetuspto-grants-1997_05
ORD IDord-a7ccb7317b164ee4b3af29b418008271
Source noteuspto-grants-1997_05