HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535472Generated: October 29, 2026
Water → Ethyl 6-[(2-methylindolizin-3-yl)carbonyl]-1-methyl-4-oxo-1,4-dihydroquinoline-3-carboxylate
https://huagongshe.com/reaction/535472
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 6-[(2-methylindolizin-3-yl)carbonyl]-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 66653314 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 6-[(2-methylindolizin-3-yl)carbonyl]-1-methyl-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 66652940 | 87.5% |
Reaction Steps
1.53 g (11.12 mmol) of potassium carbonate and 0.69 ml (11.12 mmol) of methyl iodide are added, at ambient temperature under an inter atmosphere, to 3.73 g (9.27 mmol) of ethyl 6-[(2-methylindolizin-3-yl)carbonyl]-4-oxo-1,4-dihydroquinoline-3-carboxylate in 100 ml of DMF. The reaction medium is heated at 90° C. for 2 h. 0.384 g (2.78 mmol) of potassium carbonate and 0.173 ml (2.78 mmol) of methyl iodide are added and then the heating is continued for 40 minutes. The reaction medium is hydrolysed with water and then extracted with ethyl acetate and with dichloromethane. The organic phase is washed with a saturated solution of sodium chloride, dried over sodium sulphate, and then concentrated under reduced pressure. The residue obtained is purified by silica gel column chromatography, elution being carried out with a dichloromethane/methanol (90/10) mixture. 3.15 g of a yellow solid 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-c1c23ad86939454a9a14ae50864b4a7f |
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| Source note | uspto-grants-2014_10 |
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