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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantN-bromobutanimideHCID 67184—
Reactant2,2'-Azobis(2,4-dimethylvaleronitrile)HCID 91537—
Reactant7-fluoro-1-(2-fluoro-phenyl)-3-methyl-1H-quinolin-4-oneHCID 71208935—
SolventCarbon TetrachlorideHCID 5943—
Product3-azidomethyl-7-fluoro-1-(2-fluoro-phenyl)-1H-quinolin-4-oneHCID 7120906853.6%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501732B2
Source datasetuspto-grants-2013_08
ORD IDord-c4229f9e53f0439f9ad7542f2fb8c7cf
Source noteuspto-grants-2013_08