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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370246Generated: October 30, 2026

1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)- → HCID 18467245, compound

https://huagongshe.com/reaction/370246

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-HCID 11325—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(Piperazin-1-YL)-1H-indazoleHCID 14823445—
SolventAcetonitrileHCID 6342—
ProductHCID 18467245HCID 18467245—

Reaction Steps

A suspension of 4-(1H-indazol-3-yl)piperazine (1.6 g, 7.9 mmol), N-(2-bromoethyl)phthalimide (2.1 g 7.9 mmol), and sodium bicarbonate (0.7 g, 8.3 mmol) in acetonitrile (160 ml) was warmed to reflux for 24 hours. Upon cooling to room temperature, the reaction mixture was filtered through a pad of celite and the solids were washed with DCM. The combined filtrates were concentrated to give the N-[2-[4-(1H-indazol-3-yl)-1-piperazinyl]ethyl]phthalimide which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06140345
Source datasetuspto-grants-2000_10
ORD IDord-762f4137d1b54401a33fd71f79411f65
Source noteuspto-grants-2000_10