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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744327Generated: October 30, 2026

Potassium Carbonate → HCID 21960019, compound

https://huagongshe.com/reaction/744327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantFumaric AcidHCID 444972—
Reactant6-Chloro-3-(piperidin-4-yl)benzo[d]isoxazoleHCID 13076430—
Reactant1-[4-(4-Bromobutoxy)3-methoxyphenyl]ethanoneHCID 14407171—
SolventEthanolHCID 702—
SolventAcetonitrileHCID 6342—
ProductHCID 21960019HCID 2196001971.9%

Reaction Steps

A stirred mixture of 6-chloro-3-(4-piperidinyl)-1,2-benzisoxazole (4.7 g, 20 mmol), 1-[4-(4-bromobutoxy)-3-methoxyphenyl]ethanone (6.0 g, 20 mmol), K2CO3 (2.8 g) and acetonitrile (120 ml) was refluxed for 16 hours. The reaction was allowed to cool, filtered, and the filtrate was concentrated to 9.9 g of a brown oil. The oil was chromatographed on a Waters Prep 500 utilizing silica gel columns and eluting with methylene chloride/methanol (5%). Concentration of the appropriate fractions afforded 2:3 g of an off-white solid. The solid was dissolved in ethanol and fumaric acid (0.62 g, 1.1 eq.) was added. Upon concentration of the ethanol, a crude, brown solid was collected, which was taken up in refluxing acetone. Upon cooling, a white solid crystallized from solution yielding 2.2 g (19%) of 1-[4-[4-[4-(6-chloro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-butoxy]-3-methoxyphenyl]ethanone fumarate as a white solid, m.p.=139°-141° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05559117
Source datasetuspto-grants-1996_09
ORD IDord-2889a049af6d448b87272e14c604f5c8
Source noteuspto-grants-1996_09