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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078855Generated: November 3, 2026

3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazole → HCID 15816944, compound

https://huagongshe.com/reaction/1078855

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Piperidyl)-6-fluoro-1,2-benzisoxazoleHCID 849421—
ReactantBromobutylphthalimideHCID 21960043—
SolventAcetonitrileHCID 6342—
ProductHCID 15816944HCID 1581694447.1%

Reaction Steps

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (5.5 g, 25 mmol), 4-bromobutylphthalimide (8.0 g, 28.3 mmol, 1.13 eq), K2CO 3 (4.55 g, 32 mmol) in acetonitrile (100 ml) was heated at reflux for 3 hours. At the end of the reaction, the mixture was filtered. The insolubles were washed with dichloromethane (200 ml). The organic solution was concentrated gradually to allow cystallization. The crude crystals (5.9 g) were collected. The mother liquor was concentrated to a solid (5.5 g). Purification was by flash chromatography over a silica gel column. The product (3.8 g) thus purified was recrystallized from ethanol (70 ml) to give 2.48 g of N-[4-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]butyl]phthalimide as white crystals,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05550130
Source datasetuspto-grants-1996_08
ORD IDord-00bdf6a93be843a68a5b5fc167a3b71f
Source noteuspto-grants-1996_08