HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615332Generated: October 30, 2026
Dimethylformamide → HCID 20427616, compound
https://huagongshe.com/reaction/615332
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | [7-Chloro-3-(ethoxycarbonyl)-6-fluoro-4-oxoquinolin-1(4H)-yl]methanimidic acid | HCID 3021289 | — |
| Product | HCID 20427616 | HCID 20427616 | — |
Reaction Steps
A mixture of 14.65 g (0.047 mole) of ethyl 7-chloro-6-fluoro-1-(formylamino)-1,4-dihydro-4-oxo-3-quinolinecarboxylate (Preparation 2), 12.9 g (0.094 mole) of potassium carbonate and 200 ml of dimethylformamide was stirred at 25° C. for 90 minutes. Methyl iodide (20.0 g, 0.141 mole) was then added and the reaction mixture was stirred at room temperature for 90 minutes. The dimethylformamide was removed in high vacuum at 50° C., and the residue was partitioned between 250 ml of water and 500 ml of chloroform. The chloroform layer was separated and dried over anhydrous magnesium sulfate. There was obtained from the chloroform solution upon concentration 13.8 g of ethyl 7-chloro-6-fluoro-1,4-dihydro-5-[(formyl)methylamino]-4-oxo-3-quinolinecarboxylate, m.p. 213°-216° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04499091 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-e95da60994f24d97ad839b4f273b6b29 |
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| Source note | uspto-grants-1985_02 |
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