HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899513Generated: October 28, 2026
Potassium Carbonate → 4-(6-Fluoro-1,2-benzisoxazoi-3-yl)-1-(2'-methoxyphenyl)butylpiperidine maleate
https://huagongshe.com/reaction/1899513
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Maleic Acid | HCID 444266 | — |
| Reactant | 3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazole | HCID 849421 | — |
| Reactant | 1-(4-Bromobutyl)-2-methoxybenzene | HCID 19072468 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(6-Fluoro-1,2-benzisoxazoi-3-yl)-1-(2'-methoxyphenyl)butylpiperidine maleate | HCID 86748255 | — |
Reaction Steps
A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (2.36 g, 10.7 mmole), K2CO3 (2 g, 14.5 mmol) and 2-(4-bromobutyl)anisole (2.4 g, 10 mmol) in acetonitrile (100 ml) was heated at reflux for 2.5 hours. At the end of reaction, the solvent was removed. The residue was extracted into dichloromethane (200 ml) and filtered. The dichloromethane solution was concentrated. The crude oil obtained was purified on a flash chromatography column. The material thus purified was a light yellow oil (2.73 g, 53%). This oil was dissolved in ethanol and treated with maleic acid (607 mg, 1.0 eq) in ethanol. The 4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-(2'-methoxyphenyl)butylpiperidine maleate crystals formed on concentration and subsequent cooling to 0° C. These were collected and dried to yield 2.05 g, m.p.=132°-133° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05571828 |
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| Source dataset | uspto-grants-1996_11 |
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| ORD ID | ord-d6da142b1e9442f6a806a3548e4413b8 |
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| Source note | uspto-grants-1996_11 |
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