HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413040Generated: October 29, 2026
1-(3-fluoro-4-methylphenyl)piperazine → HCID 18523254, compound
https://huagongshe.com/reaction/413040
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(3-fluoro-4-methylphenyl)piperazine | HCID 4738806 | — |
| Reactant | HCID 18523246 | HCID 18523246 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 18523254 | HCID 18523254 | 42.8% |
Reaction Steps
A stirred suspension of 1 g of ethyl 8-chloro-7,9-difluoro-4-methyl-1-oxo-1,4-dihydrobenzo[f][1,7]naphthyridine-2-carboxylate and 1.2 g of 1-(3-fluoro-4-methylphenyl)piperazine in 15 cm3 of dimethyl sulphoxide was heated to a temperature in the region of 80° C. After 20 hours, 0.6 g of 1-(3-fluoro-4-methylphenyl)piperazine was added and the heating was continued for an additional 8 hours. After 28 hours, the reaction mixture was cooled and then filtered. The precipitate was washed twice with 10 cm3 of water, twice with 5 cm3 of ethanol, and twice with 5 cm3 of diisopropyl ether. 0.64 g of ethyl 8-chloro-7-fluoro-9-[4-(3-fluoro-4-methylphenyl)piperazin-1-yl]-4-methyl-1-oxo-1,4-dihydrobenzo[f][1,7]naphthyridine-2-carboxylate was obtained in the form of a greenish-yellow solid, which melted at 350° C. with decomposition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06566362B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-7d192d0cf96d47d38f2c320cc1c12b57 |
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| Source note | uspto-grants-2003_05 |
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