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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850748Generated: November 2, 2026

Butyl iodide → 10-bromo-2-butoxy-5-(3-pyridylmethyl)-4H-pyrido[3,2,1-jk]carbazole-4-one

https://huagongshe.com/reaction/850748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl iodideHCID 10962—
ReactantPotassium CarbonateHCID 11430—
Reactant10-bromo-2-hydroxy-5-(3-pyridylmethyl)-4H-pyrido[3,2,1-jk]carbazole-4-oneHCID 15886910—
SolventDimethyl SulfoxideHCID 679—
Product10-bromo-2-butoxy-5-(3-pyridylmethyl)-4H-pyrido[3,2,1-jk]carbazole-4-oneHCID 1588692173%

Reaction Steps

10-bromo-2-hydroxy-5-(3-pyridylmethyl)-4H-pyrido[3,2,1-jk]carbazole-4-one (0.3 g) obtained in Example 2 was suspended in dimethyl sulfoxide (30 ml), and to the suspension was added potassium carbonate (0.2 g), and the mixture was stirred at room temperature for 30 minutes. 1-iodobutane (0.1 ml) was added and the mixture was stirred at room temperature for 12 hours. The reaction mixture was poured into ice water, and extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous solution of sodium chloride, washed with anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel flash column chromatography (eluent: ethyl acetate) to obtain the title compound (0.25 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06018046
Source datasetuspto-grants-2000_01
ORD IDord-82641fd2053a4f7ca6de790104f1f1a0
Source noteuspto-grants-2000_01