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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704634Generated: October 25, 2026

1-Chloro-6,7-dimethoxyisoquinoline → 6-[4-(6,7-dimethoxyisoquinolin-1-yl)-1-piperazinyl]-3,4-dihydro-2(1H)-quinolinone

https://huagongshe.com/reaction/704634

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-6,7-dimethoxyisoquinolineHCID 10640708—
Reactant6-(piperazin-1-yl)-3,4-dihydroquinolin-2(1H)-oneHCID 11117896—
SolventChloroformHCID 6212—
Solvent6-[4-(2-tert-Butoxycarbonylamino-4-methylthiazole-5-carbonyl)-1-piperazinyl]-3,4-dihydro-2(1H)-quinolinoneHCID 20072891—
Product6-[4-(6,7-dimethoxyisoquinolin-1-yl)-1-piperazinyl]-3,4-dihydro-2(1H)-quinolinoneHCID 2007278737.3%

Reaction Steps

1-Chloro-6,7-dimethoxyisoquinoline (0.63 g) and 6-(1-piperazinyl)-3,4-dihydro-2(1H)-quinolinone (1.30 g) were mixed at 200° C. for 1.5 hours under stirring. The mixture was dissolved in a mixture of chloroform and methanol (10:1 V/V) and subjected to a column chromatography on silica gel (eluent:methanol in chloroform, 0-2% V/V). The fractions containing the object compound were combined and concentrated and the residue was triturated with diisopropyl ether to give 6-[4-(6,7-dimethoxyisoquinolin-1-yl)-1-piperazinyl]-3,4-dihydro-2(1H)-quinolinone (0.44 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988698
Source datasetuspto-grants-1991_01
ORD IDord-130cfb6250e6439a9b4430a99d55c35f
Source noteuspto-grants-1991_01