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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 7-Chloro-2,3-dihydro-4-quinolone | HCID 88974 | — |
| Reactant | 2-(Dimethylamino)benzoyl chloride | HCID 22157979 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-chloro-2,3-dihydro-l-(2-dimethylaminobenzoyl)-4(lH)-quinolinone | HCID 23166854 | 96.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04968680 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-2aee0c3fa5394b8281ce63ebaae96816 |
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| Source note | uspto-grants-1990_11 |
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