Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463716Generated: October 30, 2026

1-(2-Methoxyphenyl)piperazine → Elziverine

https://huagongshe.com/reaction/463716

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantTriethylamineHCID 8471—
Reactant4-Chloromethyl-6,7-dimethoxy-1-[(3,4-dimethoxyphenyl)methyl]isoquinolineHCID 13560529—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductElziverineHCID 6583979.2%

Reaction Steps

A mixture of 10.0 g of 4-chloromethyl-6,7-dimethoxy-1-[(3,4-dimethoxyphenyl)methyl]isoquinoline, 5.5 g of 1-(2-methoxyphenyl)piperazine, and 7.6 ml of triethylamine in 100 ml of dimethylsulfoxide was heated at 80° for one hour under argon. The cooled solution was then diluted with water and extracted with methylene chloride. The organic layer was washed with sodium bicarbonate solution, dried over sodium sulfate, charcoaled, and evaporated. The residue was crystallized from ethanol to give 11.1 g of 6,7-dimethoxy-1-{(3,4-dimethoxyphenyl)methyl}-4-([4-(2-methoxyphenyl)-1-piperazinyl]methyl)isoquinoline as a yellow solid, mp 117°-119°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04544657
Source datasetuspto-grants-1985_10
ORD IDord-b3bcffabe65244d99a28b1e91f743bfb
Source noteuspto-grants-1985_10