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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850763Generated: November 1, 2026

2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 10-bromo-2-methoxy-4H-pyrido[3,2,1-jk]carbazole-4-one

https://huagongshe.com/reaction/850763

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantSodium HydroxideHCID 14798—
Reactant10-bromo-5,6-dihydro-2-methoxy-4H-pyrido[3,2,1-jk]carbazole-4-oneHCID 9883956—
Solvent1,4-DioxaneHCID 31275—
Product10-bromo-2-methoxy-4H-pyrido[3,2,1-jk]carbazole-4-oneHCID 2125288281.1%

Reaction Steps

10-bromo-5,6-dihydro-2-methoxy-4H-pyrido[3,2,1-jk]carbazole-4-one (3.6 g) obtained in Example 1, step 3 was dissolved in anhydrous dioxane (300 ml), and DDQ (3.0 g) was added at room temperature. The mixture was heated under reflux in an argon atmosphere for 5 hours. After allowing to cool, the reaction mixture was added to 1N aqueous solution of sodium hydroxide (500 ml), and extracted with ethyl acetate. The ethyl acetate layer was washed with 1N aqueous solution of sodium hydroxide and saturated aqueous solution of sodium chloride in succession, dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: methylene chloride containing 3% methanol) to obtain the title compound (2.9 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06018046
Source datasetuspto-grants-2000_01
ORD IDord-30c22d1c54134759bd88abb72bddf8bd
Source noteuspto-grants-2000_01