HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398420Generated: November 3, 2026
Selenium Dioxide → 8-Chloro-6-methyl-5-oxo-5,6-dihydrobenzo[c][2,7]naphthyridine-4-carbaldehyde
https://huagongshe.com/reaction/1398420
Participants
| Role | Name | HCID | Charge |
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| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | 8-Chloro-4,6-dimethyl-5H,6H-benzo[c]2,7-naphthyridin-5-one | HCID 86710337 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 8-Chloro-6-methyl-5-oxo-5,6-dihydrobenzo[c][2,7]naphthyridine-4-carbaldehyde | HCID 86710409 | 52.2% |
Reaction Steps
To a solution of 8-chloro-4,6-dimethylbenzo[c][2,7]naphthyridin-5(6H)-one (100 mg, 0.387 mmol), prepared as described in Example 16, Part G, in AcOH (4 mL) was added selenium dioxide (51.5 mg, 0.464 mmol). The reaction mixture was allowed to stir at 70° C. for 3 h. Volatiles were removed under reduced pressure and the residue so obtained was dissolved in dichloromethane (2 mL). The mixture was filtered through diatomaceous earth (Celite®) and the filtrate was concentrated under reduced pressure to afford the title product (0.1 g, 0.202 mmol, 52% crude yield) as pale yellow solid. The material was carried on without further purification. LC/MS, (ESI) m/z 273.0 [(M+H)+, calcd for C14H10ClN2O2, 273.0]; LC/MS retention time (method H): tR=1.89 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901305B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-188646fe07af48278ef7b964391dacd7 |
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| Source note | uspto-grants-2014_12 |
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