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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235479Generated: October 30, 2026

Hydrochloric Acid → 3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl-2-hydroxy-1-propyl]-2,3-dihydro-1H-isoindole dihydrochloride

https://huagongshe.com/reaction/235479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactanto-Bis(bromomethyl)benzeneHCID 66665—
Reactant3-Amino-2-hydroxypropyl-4-(6-fluoro-1,2-benzisoxazol-yl)piperidineHCID 86749761—
SolventEthanolHCID 702—
Product3-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl-2-hydroxy-1-propyl]-2,3-dihydro-1H-isoindole dihydrochlorideHCID 86750249—

Reaction Steps

To a stirred mixture of 1-(3-amino-2-hydroxypropyl-4-(6-fluoro-1,2-benzisoxazol3-yl)piperidine (2.24 g, 7.6 mmol), K2CO3 (1.61 g, 11.7 mmol) in acetonitrile (100 ml) was added α,α'-dibromo-o-xylene (1.54 g, 6.1 mmol). The mixture was heated at reflux for 4 hours then cooled. The insolubles were filtered. The dark red solution was concentrated down. The residue was purified by flash chromatography over s silica gel column (SiO2, 30 g; eluted with 1% CH3OH in dichloromethane). The product so obtained weighed 940 mg as an oil. This oil was dissolved in ethanol and was treated with a solution of HCl in ethanol (188 mg of AcCl in ethanol). The dark solids were collected and recrystallized again in ethanol to yield off-white crystals (1.01 g), m.p. 240°-243° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597842
Source datasetuspto-grants-1997_01
ORD IDord-1517c296472343a1a962f207a244c54e
Source noteuspto-grants-1997_01