HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394956Generated: October 25, 2026
Diethyl (ethoxymethylene)malonate → diethyl [N-cyclopropyl-N-[3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitrophenyl]amino-methylene]malonate
https://huagongshe.com/reaction/2394956
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| Reactant | 3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitro-N-cyclopropylaniline | HCID 18974495 | — |
| Product | diethyl [N-cyclopropyl-N-[3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitrophenyl]amino-methylene]malonate | HCID 19418744 | — |
Reaction Steps
To 3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitro-N-cyclopropylaniline (1.57 g) is added diethyl ethoxymethylenemalonate (1.45 ml) and the mixture is heated at 150° C. for 25 hours. After cooling, the reaction product is purified by silica-gel column-chromatography (dichloromethane:methanol=100:1) to give diethyl [N-cyclopropyl-N-[3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitrophenyl]aminomethylene]malonate (1.50 g). The product is dissolved in acetic anhydride (7.9 ml) and thereto conc. sulfuric acid (3.16 ml) is added dropwise at 50°-60° C., followed by stirring for 30 minutes. The resultant mixture is poured into ice-water, neutralized, extracted with dichloromethane and the extract is dried. The solvent is distilled off under reduced pressure. Purification by silica-gel column-chromatography (dichloromethane:methanol=10:1) to give ethyl 7-(1-piperazinyl)-1-cyclopropyl-6-fluoro-5-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylate (26 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05811576 |
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| Source dataset | uspto-grants-1998_09 |
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| ORD ID | ord-4afaba8e2a2d4501bbf300fead1ee85c |
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| Source note | uspto-grants-1998_09 |
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