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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073062Generated: October 25, 2026

Pyridine → 7-chloro-2,3-dihydro-l-(2-dimethylaminobenzoyl)-4(lH)-quinolinone

https://huagongshe.com/reaction/1073062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1,4-DioxaneHCID 31275—
Reactant7-Chloro-2,3-dihydro-4-quinoloneHCID 88974—
Reactant2-(Dimethylamino)benzoyl chlorideHCID 22157979—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product7-chloro-2,3-dihydro-l-(2-dimethylaminobenzoyl)-4(lH)-quinolinoneHCID 2316685496.7%

Reaction Steps

To a mixture of 7-chloro-2,3-dihydro-4(lH)-quinolinone (20 g), pyridine (26 g) and dioxane (200 ml) was added dropwise 2-dimethylaminobenzoyl chloride (30 g) under cooling at 0° C. to 5° C. with stirring. The mixture was allowed to react at room temperature for additional 3 hours. The reaction mixture was poured into 500 ml of water, then shaken with additional dichloromethane (1000 ml). The organic layer was washed once with 1 N HCl (100 ml), twice with water (200 ml each) then once with saturated aqueous NaCl solution and dried over anhydrous sodium sulfate. Dichloromethane was removed in vacuo and the residue was recrystallized with dichloromethane and n-hexane to obtain 7-chloro-2,3-dihydro-l-(2-dimethylaminobenzoyl)-4(lH)-quinolinone (yield 35 g) as white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968680
Source datasetuspto-grants-1990_11
ORD IDord-2aee0c3fa5394b8281ce63ebaae96816
Source noteuspto-grants-1990_11