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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1456742Generated: October 31, 2026

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

https://huagongshe.com/reaction/1456742

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), K2 CO3 (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, m.p.=144°-146° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843977
Source datasetuspto-grants-1998_12
ORD IDord-410f199545084a828025da6b4e5eb283
Source noteuspto-grants-1998_12