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HRID 1762806Erstellt: 25. Oktober 2026

Acetic Anhydride → 5,14-Dihydro-2-hydroxy-7-methylbenz[5,6]isoindolo[2,1-b]isoquinoline-8,13-dione

https://huagongshe.com/reaction/1762806

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AnhydrideHCID 7918—
Edukt1,4-NaphthoquinoneHCID 8530—
Edukt1,2,3,4-Tetrahydro-6-hydroxy-3-isoquinolinecarboxylic acidHCID 2733174—
Produkt5,14-Dihydro-2-hydroxy-7-methylbenz[5,6]isoindolo[2,1-b]isoquinoline-8,13-dioneHCID 20039736—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 6-hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (2 g) and 1,4-naphthalenedione (3.4 g) in acetic anhydride (150 ml) was stirred in an oil bath at 100° C. for 15 minutes. It was then allowed to cool to room temperature and the green solid (2.74 g) was collected by filtration, washed with acetic anhydride and ether and dried at 100° C. for 2 h in vacuo, to give the title compound m.p. 275°-320° C. (decomp), λmax (in ethanol) 244.5 nm (ε26,220) 318 nm (ε4,510) and 383 nm (ε6,390).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04835158
Quelldatensatzuspto-grants-1989_05
ORD IDord-6198ae7700ac4ce88b270b9d86940696
Quellennotizuspto-grants-1989_05