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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449935Generated: October 31, 2026

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

https://huagongshe.com/reaction/1449935

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. ANALYSIS: Calculated for C17H24FN3O2.C4H4O4 : 55.86%C 6.00%H 7.82%N Found: 56.11%C 5.94%H 7.86%N

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599821
Source datasetuspto-grants-1997_02
ORD IDord-a556b3bef2ce420eb0ba2fc9e2e1a7ae
Source noteuspto-grants-1997_02