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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073064Generated: November 1, 2026

Pyridine → HCID 23054596, compound

https://huagongshe.com/reaction/1073064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant7-Chloro-2,3-dihydro-4-quinoloneHCID 88974—
ReactantHCID 22414448HCID 22414448—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 23054596HCID 2305459683.2%

Reaction Steps

To a mixture of 7-chloro-2,3-dihydro-4(lH)-quinolinone (20.0 g), pyridine (26 g) and dichloromethane (200 ml) was added dropwise 2-methyl-3-thienylcarbonyl chloride (26 g) at room temperature with stirring. The mixture was stirred under reflux for 4 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) and once with saturated aqueous NaCl solution, then dried over anhydrous sodium sulfate. Solvent was removed in vacuo and 7-chloro-2,3-dihydro-l-(2-methyl-3-thienylcarbonyl)-4(lH)-quinolinone (yield 28 g) was obtained as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04968680
Source datasetuspto-grants-1990_11
ORD IDord-7c3fa7a32f314888a1740e943cb33069
Source noteuspto-grants-1990_11