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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2184608Generated: October 29, 2026

Acetonitrile → 2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-ethoxyphtalimide hemihydrate

https://huagongshe.com/reaction/2184608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethoxy)-HCID 199875—
Reactant3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
Product2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-ethoxyphtalimide hemihydrateHCID 131719737—

Reaction Steps

A mixture of 3-(4-piperidinyl)-6-fluorobenzisoxazole (3.42 g, 15 mmol), N-(2-bromoethoxy)-phthalimide (4.3 g, 16 mmol) and K2CO3 (26 g, 18 mmol) in acetonitrile (150 ml) was heated at reflux for 2 hours. The solids were removed and the solvent was evaporated. The residue was purified over a flash chromatography column (packed with SiO2, 60 g: eluted with dichloromethane (DCM) and 1% CH3OH in DCM. The pure product thus obtained, weighing 6.8 g was crystallized from DCM:ethanol. Recrystallization from ethanol and i-propyl ether yielded white crystals (2.4 g, m.p. 125°-127° C.) as the hemihydrate. ANALYSIS: Calculated for C22H20N3O4.0.5.H2O: 63.15%C 5.05%H 10.04%N 2.15%H2O Found: 63.20%C 5.16%H 9.80%N 2.32%H2O

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037729E1
Source datasetuspto-grants-2002_06
ORD IDord-1e430b41ba724747931ee9073fc125f8
Source noteuspto-grants-2002_06