HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525958Generated: October 28, 2026
Sodium → Ethyl 1-ethyl-5,6-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate
https://huagongshe.com/reaction/525958
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 1-ethyl-5,6-dimethoxy-1H-benzo[d][1,3]oxazine-2,4-dione | HCID 86732823 | — |
| Reactant | (Z)-3-ethoxy-3-oxoprop-1-en-1-olate | HCID 86732825 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 1-ethyl-5,6-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 86732824 | 33.9% |
Reaction Steps
Under N2, 1-ethyl-5,6-dimethoxy-1H-benzo[d][1,3]oxazine-2,4-dione (12 g, 43.5 mmol) in N,N-Dimethylformamide (DMF) (250 mL) was added to a solution of (Z)-3-ethoxy-3-oxoprop-1-en-1-olate, Sodium salt (18.01 g, 130 mmol) in N,N-Dimethylformamide (DMF) (150 mL) with stirring. The resulting solution was stirred at 110° C. for 3 h. After cooling down, the mixture was concentrated in vacuo and the orange residue was taken up in water. The aqueous solution was washed with ethyl ether (3×), acidified to pH˜2 with 6 N HCl, and extracted with DCM (4×). The organic extracts were dried over Na2SO4, filtered and concentrated. The residue was purified by normal phase silica gel chromatography (CombiFlash), eluting with MeOH/DCM (0-15%) to afford ethyl 1-ethyl-5,6-dimethoxy-4-oxo-1,4-dihydroquinoline-3-carboxylate (4.5 g, 14.74 mmol, 33.9% yield) as a brown oil that turned into a brown solid after overnight. LCMS: (M+H)+: 306.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09340556B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-67ed1d5c32ca43eabcea7efd539ba8a0 |
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| Source note | uspto-grants-2016_05 |
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