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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236639Generated: October 26, 2026

2-Methoxy-5-[(methylamino)methyl]phenol → (4Z)-6-bromo-4-{[(3-hydroxy-4-methoxybenzyl)(methyl)amino]methylene}isoquinoline-1,3(2H,4H)-dione

https://huagongshe.com/reaction/2236639

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methoxy-5-[(methylamino)methyl]phenolHCID 1519937—
Reactant(E)-6-bromo-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dioneHCID 68692760—
SolventTetrahydrofuranHCID 8028—
Product(4Z)-6-bromo-4-{[(3-hydroxy-4-methoxybenzyl)(methyl)amino]methylene}isoquinoline-1,3(2H,4H)-dioneHCID 4262551895%

Reaction Steps

(4E)-6-Bromo-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione (0.15 g, 0.53 mmol) and 2-methoxy-5-methylaminomethyl-phenol (80 mg, 0.48 mmol) were stirred in tetrahydrofuran (10 mL) at room temperature. The reaction mixture is concentrated under reduced pressure. The solid material is then collected, washed with diethyl ether, water, and methanol, and then dried under vacuum to give (4Z)-6-bromo-4-{[(3-hydroxy-4-methoxybenzyl)(methyl)amino]methylene}isoquinoline-1,3(2H,4H)-dione as a yellow solid (0.19 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-a0d916b536804624a7cca8fce0f46ee8
Source noteuspto-grants-2010_05