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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079556Generated: October 30, 2026

Potassium Carbonate → 1-(3-Dimethylaminopropyl)-4-(6-fluoro-1,2-benzisoxazol-yl)piperidine difumarate

https://huagongshe.com/reaction/1079556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Dimethylamino)propyl chloride hydrochlorideHCID 94308—
ReactantFumaric AcidHCID 444972—
Reactant3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product1-(3-Dimethylaminopropyl)-4-(6-fluoro-1,2-benzisoxazol-yl)piperidine difumarateHCID 6707110056.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (3.05 g, 13.8 mmol), 3-dimethylaminopropyl chloride hydrochloride (3.4 g, 21 mmol), K2CO3 (6.2 g, 45 mmol), tetrabutylammonium hydrogen sulfate (phase transfer catalyst, 1.5 g) in acetonitrile (100 ml) and water (50 ml) was heated at 60° C. overnight. The aqueous phase was separated, and acetonitrile was removed at reduced pressure. The residue was extracted into DCM. The organic solution was washed with H2O and brine, then dried with MgSO4. The solvent was removed and the crude product (4.3 g) was treated with fumaric acid (1.58 g, 1.0 eq) in dilute ethanol. The crystals were collected (2.53 g), m.p.=192°-194° C. Recrystallization from ethanol yielded 2.08 g of white crystals, mp=194°-195° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580875
Source datasetuspto-grants-1996_12
ORD IDord-54630e49f0d2472f922e68864cabb8b4
Source noteuspto-grants-1996_12