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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850756Generated: October 31, 2026

Potassium Iodide → 10-bromo-5-methyl-2-i-propoxycarbonylmethyloxy-5-(3-pyridylmethyl)-4H-pyrido[3,2,1-jk]carbazole-4-one

https://huagongshe.com/reaction/850756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantIsopropyl bromoacetateHCID 121593—
Reactant10-bromo-2-hydroxy-5-methyl-4H-pyrido [3,2,1-jk]carbazole-4-oneHCID 21252842—
SolventDimethyl SulfoxideHCID 679—
Product10-bromo-5-methyl-2-i-propoxycarbonylmethyloxy-5-(3-pyridylmethyl)-4H-pyrido[3,2,1-jk]carbazole-4-oneHCID 1936489367%

Reaction Steps

10-bromo-2-hydroxy-5-methyl-4H-pyrido[3,2,1-jk]carbazole-4-one (250 mg) obtained in Example 49 was suspended in dimethyl sulfoxide (10 ml), and potassium carbonate (210 mg) was added to the suspension. The mixture was stirred at room temperature for 30 minutes and i-propyl bromoacetate (0.12 ml) and potassium iodide (1 grain) were added in succession, and the mixture was stirred at room temperature for 12 hours. The reaction mixture was poured into ice water (50 ml) and extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel flash column chromatography (eluent: ethyl acetate), and the crude purification product was washed with ether and recovered by filtration to obtain the title compound (220 mg, 67%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06018046
Source datasetuspto-grants-2000_01
ORD IDord-e78a6e8adf514b3aa2286388a3aaaa0c
Source noteuspto-grants-2000_01