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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 704634Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/704634

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Chloro-6,7-dimethoxyisoquinolineHCID 10640708—
Edukt6-(piperazin-1-yl)-3,4-dihydroquinolin-2(1H)-oneHCID 11117896—
LösungsmittelChloroformHCID 6212—
Lösungsmittel6-[4-(2-tert-Butoxycarbonylamino-4-methylthiazole-5-carbonyl)-1-piperazinyl]-3,4-dihydro-2(1H)-quinolinoneHCID 20072891—
Produkt6-[4-(6,7-dimethoxyisoquinolin-1-yl)-1-piperazinyl]-3,4-dihydro-2(1H)-quinolinoneHCID 2007278737,3%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04988698
Quelldatensatzuspto-grants-1991_01
ORD IDord-130cfb6250e6439a9b4430a99d55c35f
Quellennotizuspto-grants-1991_01