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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085782Generated: November 1, 2026

Piperazine → ethyl 6,8-difluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate

https://huagongshe.com/reaction/1085782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium CarbonateHCID 11430—
Reactantethyl 6,7,8-trifluoro-1-methyl-4-oxo-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylateHCID 9973824—
SolventDimethylformamideHCID 6228—
Productethyl 6,8-difluoro-1-methyl-4-oxo-7-(1-piperazinyl)-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylateHCID 1000076473.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

Ethyl 6,7,8-trifluoro-1-methyl-4-oxo-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylate (0.33 g) and 0.14 g of potassium carbonate were suspended in 10 ml of N,N-dimethylformamide, 0.13 g of anhydrous piperazine was added and the mixture was stirred at 60° C. for 2 hours. N,N-Dimethylformamide was evaporated therefrom in vacuo, the residue was dissolved in chloroform, the solution was washed with water, dried over magnesium sulfate, the solvent was evaporated therefrom, the residue was subjected to a silica gel column chromatography (30 g of Wakogel C-300 being used) and eluted with chloroform-methanol (4:1) to give 0.29 g of the title product, m.p. 195°-198° C. (decompn).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011831
Source datasetuspto-grants-1991_04
ORD IDord-02a4579fc57b49e782eaf4c5f508d360
Source noteuspto-grants-1991_04