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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887806Generated: November 2, 2026

Dimethylformamide → 3-azidomethyl-7-chloro-1-(2-chloro-phenyl)-1H-quinolin-4-one

https://huagongshe.com/reaction/1887806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium AzideHCID 33557—
Reactant3-bromomethyl-7-chloro-1-(2-chloro-phenyl)-1H-quinolin-4-oneHCID 86675766—
SolventEthyl AcetateHCID 8857—
Product3-azidomethyl-7-chloro-1-(2-chloro-phenyl)-1H-quinolin-4-oneHCID 7120867658.2%

Reaction Steps

To a 25 mL round-bottom flask containing the crude 3-bromomethyl-7-chloro-1-(2-chloro-phenyl)-1H-quinolin-4-one (410 mg, 1.07 mmol) was added sodium azide (83.5 mg, 1.28 mmol) and DMF (9 mL). The reaction mixture was stirred overnight at room temperature. The mixture was diluted with ethyl acetate (100 mL) and washed with brine (100 mL). The organic layer was dried over magnesium sulfate, filtered, and concentrated. The crude was purified by flash chromatography (silica gel, 24 g, 0-50% ethyl acetate in hexanes) to yield 3-azidomethyl-7-chloro-1-(2-chloro-phenyl)-1H-quinolin-4-one (215 mg, 58%) as a light yellow solid. 1H NMR (DMSO-d6) δ ppm 8.17-8.36 (m, 2H) 7.83 (ddd, J=9.8, 7.9, 1.7 Hz, 2H) 7.68 (ddd, J=9.8, 7.8, 1.6 Hz, 2H) 7.48 (dd, J=8.7, 1.8 Hz, 1H) 6.70 (d, J=1.8 Hz, 1H) 4.09-4.44 (m, 2H). MS calcd. for C16H10Cl2N4O [(M+H)+] 346.0, obsd. 345.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501732B2
Source datasetuspto-grants-2013_08
ORD IDord-46b9c8e864ed4dd5804ade0684c85239
Source noteuspto-grants-2013_08