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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211554Generated: October 29, 2026

3,6-Dichlorophthalic anhydride → N-[2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-3,6-dichlorophthalimide

https://huagongshe.com/reaction/2211554

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,6-Dichlorophthalic anhydrideHCID 78218—
Reactant2-(4-(6-Fluorobenzo[d]isoxazol-3-yl)piperidin-1-yl)ethan-1-amineHCID 14699857—
SolventDichloromethaneHCID 6344—
ProductN-[2-[4-(6-Fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-3,6-dichlorophthalimideHCID 15340828—

Reaction Steps

A mixture of 2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethylamine (2.44 gm, 9.24 mmoles) and 3,6-dichlorophthalic anhydride (2.01 gm; 9.27 mmoles) in dichloromethane (DCM, 50 ml) was stirred at room temperature for hr. White precipitates formed and the TLC of the reaction mixture showed that there was no starting amine remaining. The solvent was stripped down and the white solids which were poorly soluble in DCM were loaded onto a flash chromatography column. (SiO2; 30 gm) and the column was eluted with a solution of 1% CH3OH in DCM. The desired product thus obtained weighed 2.29 gm (54%). Recrystallization from hot ethanol yielded 2.15 gm of white crystals, m.p.=163°-164° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE039265E1
Source datasetuspto-grants-2006_09
ORD IDord-28c2d9ab68a742e08c90bcfd5f6a1f21
Source noteuspto-grants-2006_09