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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968067Generated: October 31, 2026

Water → Ethyl 3-(4-(dimethylcarbamoyl)phenyl)-2-(4-fluorophenyl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylate

https://huagongshe.com/reaction/1968067

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium ethoxideHCID 2723922—
Reactant4-formyl-N,N-dimethylbenzamideHCID 10559205—
ReactantHCID 178519076HCID 178519076—
SolventEthyl PropionateHCID 7749—
SolventEthyl AcetateHCID 8857—
ProductEthyl 3-(4-(dimethylcarbamoyl)phenyl)-2-(4-fluorophenyl)-4-oxo-1,2,3,4-tetrahydroquinoline-5-carboxylateHCID 6726167044%

Reaction Conditions

Temperature30 °C

Reaction Steps

Sodium (115 mg, 5 mmol) was added to EtOH (10 mL) to afford sodium ethoxide. (E)-4-(4-fluorobenzylideneamino)isobenzofuran-1(3H)-one (500 mg, 1.96 mmol) and 4-formyl-N,N-dimethylbenzamide (382 mg, 2.16 mmol) were dissolved in ethyl propionate (10 mL), and the sodium ethoxide solution was added dropwise to the mixture at 0° C., then the mixture were heated to 30° C. for 1 h. To the reaction mixture was added water and EtOAc, the organic phase was separated, washed with water and brine. The organic phase was dried over anhydrous sodium sulfate and then concentrated to afford the crude product. The crude product was purified by flash chromatography (MeOH:DCM 1:25) to give the title compound (400 mg, yield 44%). LC-MS (ESI) m/z: 461 (M+1)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420650B2
Source datasetuspto-grants-2013_04
ORD IDord-bbace241b0cb42d0a24b854d8e1f546f
Source noteuspto-grants-2013_04