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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251267Generated: November 3, 2026

1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinoline → HCID 22502713, compound

https://huagongshe.com/reaction/1251267

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Ethylpiperazin-4-yl)-3-bromoisoquinolineHCID 22502447—
ReactantHCID 178467830HCID 178467830—
CatalystHCID 178418745HCID 178418745—
SolventDiethyl EtherHCID 3283—
ProductHCID 22502713HCID 2250271359.5%

Reaction Steps

To a mixture solution of 1-(4-ethylpiperazin-1-yl)-3-bromoisoquinoline (0.71 g) cooled to 0° C. and [1,3-bis(diphenylphosphino)propane]dichloronickel(II) (0.05 g) in diethyl ether (20 ml) was dropwise added 1M benzylmagnesium chloride/ether solution (4.5 ml) in nitrogen atmosphere. The reaction mixture was stirred at room temperature overnight. The reaction solution was diluted with ether (30 ml), washed with water and brine, and then dried over magnesium sulfate. The solvent was removed, and the resulting residue was purified by silica gel column chromatography (ethyl acetate/acetone system), to give the title compound (0.44 g; 59.5%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340759B1
Source datasetuspto-grants-2002_01
ORD IDord-21c92eb7b9924b16bcc993ecf304f125
Source noteuspto-grants-2002_01