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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814441Generated: October 27, 2026

1-(4-Ethylpiperazin-1-yl)-3-(4-methoxyphenyl)isoquinoline → 1-(1-Ethylpiperazin-4-yl)-3-(4-hydroxyphenyl)isoquinoline

https://huagongshe.com/reaction/1814441

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Ethylpiperazin-1-yl)-3-(4-methoxyphenyl)isoquinolineHCID 9950168—
SolventHydrogen BromideHCID 260—
Product1-(1-Ethylpiperazin-4-yl)-3-(4-hydroxyphenyl)isoquinolineHCID 13571904275%

Reaction Steps

1-(4-Ethylpiperazin-1-yl)-3-(4-methoxyphenyl)isoquinoline (1.50 g) obtained in Example 10 was dissolved in 48% hydrobromic acid (15 ml) and reacted at 120° C. for 1.5 hr. The reaction solution was evaporated to a final half volume, and ice-cooled. The resulting precipitates were collected by filtration, and then washed with a small amount of ice-cooled water. The precipitates were treated with a 2N aqueous solution of sodium hydroxide, followed by collecting the precipitates by filtration, washed with water and ether/n-hexane, and then dried in warm air, to give the title compound (1.08 g, yield; 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-6df015cfc08f4395b2b080a6922a4e10
Source noteuspto-grants-2005_04