HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887812Generated: October 28, 2026
Sodium Azide → 3-azidomethyl-7-fluoro-1-(2-fluoro-phenyl)-1H-quinolin-4-one
https://huagongshe.com/reaction/1887812
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,2'-Azobis(2,4-dimethylvaleronitrile) | HCID 91537 | — |
| Reactant | 7-fluoro-1-(2-fluoro-phenyl)-3-methyl-1H-quinolin-4-one | HCID 71208935 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-azidomethyl-7-fluoro-1-(2-fluoro-phenyl)-1H-quinolin-4-one | HCID 71209068 | 53.6% |
Reaction Steps
In a 50 mL round bottom flask, 7-fluoro-1-(2-fluoro-phenyl)-3-methyl-1H-quinolin-4-one (1.20 g, 4.42 mmol), N-bromosuccinimide (0.787 g, 4.42 mmol) and V65 [2,2′-azobis(2,4-dimethylvaleronitrile)](0.33 g, 1.33 mmol) were combined with carbon tetrachloride (35.0 mL). The reaction mixture was heated to reflux for 5 hr. The reaction was concentrated to dryness and the crude (containing 3-bromomethyl-7-fluoro-1-(2-fluoro-phenyl)-1H-quinolin-4-one) was redissolved in DMF (10.0 mL). To this reaction mixture was added sodium azide (1.44 g, 22.1 mmol) and the reaction was stirred at room temperature overnight. The reaction was partitioned between ethyl acetate and water and the organic layer was washed with saturated aqueous sodium bicarbonate solution. The organic layer was evaporated to dryness and purified by flash chromatography using 40% ethyl acetate-hexanes to afford 3-azidomethyl-7-fluoro-1-(2-fluoro-phenyl)-1H-quinolin-4-one (740 mg, 53.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501732B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-c4229f9e53f0439f9ad7542f2fb8c7cf |
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| Source note | uspto-grants-2013_08 |
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