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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-fluoro-4-methylphenyl)piperazineHCID 4738806—
ReactantHCID 18523246HCID 18523246—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 18523254HCID 1852325442.8%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566362B2
Source datasetuspto-grants-2003_05
ORD IDord-7d192d0cf96d47d38f2c320cc1c12b57
Source noteuspto-grants-2003_05