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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814585Generated: November 3, 2026

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

https://huagongshe.com/reaction/1814585

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 numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-d02cc860ed2449429f4b50ca4e01316f
Source noteuspto-grants-2005_04