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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Butyl iodide | HCID 10962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 10-bromo-2-hydroxy-5-(3-pyridylmethyl)-4H-pyrido[3,2,1-jk]carbazole-4-one | HCID 15886910 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 10-bromo-2-butoxy-5-(3-pyridylmethyl)-4H-pyrido[3,2,1-jk]carbazole-4-one | HCID 15886921 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06018046 |
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| Source dataset | uspto-grants-2000_01 |
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| ORD ID | ord-82641fd2053a4f7ca6de790104f1f1a0 |
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| Source note | uspto-grants-2000_01 |
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