HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535471Generated: October 30, 2026
Diethyl (ethoxymethylene)malonate → Ethyl 6-[(2-methylindolizin-3-yl)carbonyl]-4-oxo-1,4-dihydroquinoline-3-carboxylate
https://huagongshe.com/reaction/535471
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | (4-Aminophenyl)(2-methylindolizin-3-yl)methanone | HCID 66653274 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diphenyl Ether | HCID 7583 | — |
| Product | Ethyl 6-[(2-methylindolizin-3-yl)carbonyl]-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 66653314 | — |
Reaction Steps
1.69 ml of diethyl ethoxymethylene malonate are added, under an inert atmosphere at ambient temperature, to 1.83 g (6.8 mmol) of (4-aminophenyl)(2-methylindolizin-3-yl)methanone in 23 ml of toluene. The reaction medium is heated at 110° C. for 1 h 45 and then concentrated under reduced pressure. The residue obtained is dissolved in 45 ml of diphenyl ether and then heated at 230° C. for 30 minutes. After the addition of diisopropyl ether at ambient temperature, the precipitate formed is filtered off, rinsed with diisopropyl ether, with methanol and then with dichloromethane, and dried under reduced pressure at 50° C. overnight 1.2 g of a yellow powder are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859544B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-87f3b63dde16412587c986174b51708d |
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| Source note | uspto-grants-2014_10 |
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