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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073761Generated: November 3, 2026

1-Cyclopropyl-6-fluoro-7-(4-formyl-3-methyl-1-piperazinyl)-5-methyl-4-oxo-3-formyl1,2,3,4-tetrahydroquinoline → 1-Cyclopropyl-6-fluoro-7-(4-formyl-3-methyl-1-piperazinyl)-5-methyl-3-formyl-1,4-dihydro-4oxoquinoline

https://huagongshe.com/reaction/1073761

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Cyclopropyl-6-fluoro-7-(4-formyl-3-methyl-1-piperazinyl)-5-methyl-4-oxo-3-formyl1,2,3,4-tetrahydroquinolineHCID 15712725—
CatalystHCID 178418406HCID 178418406—
SolventMethanolHCID 887—
Product1-Cyclopropyl-6-fluoro-7-(4-formyl-3-methyl-1-piperazinyl)-5-methyl-3-formyl-1,4-dihydro-4oxoquinolineHCID 1571272798%

Reaction Steps

1-Cyclopropyl-6-fluoro-7-(4-formyl-3-methyl-1-piperazinyl)-5-methyl-4-oxo-3-formyl-1,2,3,4-tetrahydroquinoline (4.0 g) is dissolved in methanol (150 ml) and thereto is added manganese dioxide (9.3 g), and the mixture is stirred at room temperature for 2 hours. After removing manganese dioxide by filtration with celite, the filtrate is concentrated, and the resulting residue is recrystallized from ethanol to give 1-cyclopropyl-6-fluoro-7-(4-formyl-3 -methyl-1-piperazinyl)-5-methyl-3-formyl-1,4-dihydro-4oxoquinoline (3.9 g), as pale yellow powdery crystals, m.p. 258°-260° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971970
Source datasetuspto-grants-1990_11
ORD IDord-5d328b6897474bb191e0dc07d4a43907
Source noteuspto-grants-1990_11