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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477013Generated: October 29, 2026

1-Piperazinecarboxaldehyde → HCID 14304585, compound

https://huagongshe.com/reaction/477013

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PiperazinecarboxaldehydeHCID 82191—
Reactant1-Cyclopropyl-5,6,7,8-tetrafluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 13825515—
SolventPyridineHCID 1049—
ProductHCID 14304585HCID 1430458560.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 1-cyclopropyl-5,6,7,8-tetrafluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (2.0 g), 4-formylpiperazine (0.75 g), and pyridine (30 ml) was stirred at 50° C. for 1 hour. The reaction mixture was concentrated to dryness under reduced pressure. The residue was mixed with water and extracted with chloroform. The extract was dried, and chloroform was evaporated. Ethanol was added to the residue, and the precipitated crystals were collected by filtration. Recrystallization from chloroform-ethanol gave 1-cyclopropyl-5,6,8-trifluoro-7-(4-formyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (1.58 g), m.p. 290°-297° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886810
Source datasetuspto-grants-1989_12
ORD IDord-0a3cfa4dd6f54e39beac71158c90bb25
Source noteuspto-grants-1989_12