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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1636277Generated: November 1, 2026

1-(2-Pyrimidinyl)piperazine → HCID 464016, compound

https://huagongshe.com/reaction/1636277

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Pyrimidinyl)piperazineHCID 88747—
Reactant1-Cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxo-8-trifluoromethyl-3-quinolinecarboxylic acidHCID 14278830—
SolventPyridineHCID 1049—
ProductHCID 464016HCID 46401647.5%

Reaction Conditions

Temperature105 °C

Reaction Steps

In 20 ml of pyridine were dissolved 1.0 g (0.003 mole) of 1-cyclopropyl-6,7-difluoro-8-trifluoromethyl-1,4-dihydro-4-oxoquinoline-3-carboxylic acid and 1.23 g (0.0075 mole) of 1-(2-pyrimidinyl)piperazine, and the mixture was stirred at 105° C. for 3 hours. Then, the solvent was removed by evaporation under reduced pressure, and the residue was applied to silica gel column chromatography (eluent; a chloroform:methanol=9.5:0.5 mixed solution) to obtain 0.68 g of 1-cyclopropyl-6-fluoro-8-trifluoromethyl-1,4-dihydro-4-oxo-7-[4-(2-pyrimidinyl)piperazin-1-yl]quinoline-3-carboxylic acid as yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06034086
Source datasetuspto-grants-2000_03
ORD IDord-d956571309424f93a77dbd0d5ef3e08c
Source noteuspto-grants-2000_03