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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369299Generated: October 28, 2026

Pyridine → 1-(5-Amino-2,4-difluorophenyl)-8-chloro-6-fluoro-7-(2,2,2-trifluoroethylamino)-4-oxo-1,4-dihydroquinoline-3-carboxylic Acid

https://huagongshe.com/reaction/369299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthanamine, 2,2,2-trifluoro-HCID 9773—
Reactant1-(3-Amino-4,6-difluorophenyl)-8-chloro-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acidHCID 10861999—
SolventDiethyl EtherHCID 3283—
Product1-(5-Amino-2,4-difluorophenyl)-8-chloro-6-fluoro-7-(2,2,2-trifluoroethylamino)-4-oxo-1,4-dihydroquinoline-3-carboxylic AcidHCID 2328472867.9%

Reaction Conditions

Temperature40 °C

Reaction Steps

2,2,2-Trifluoroethylamine (50 mg) and pyridine (300 ml) were added to 1-(5-amino-2,4-difluorophenyl)-8-chloro-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (110 mg), and the mixture was stirred at 40° C. for 2 days. Additional 2,2,2-trifluoroethylamine (50 mg) was added, and the mixture was stirred at 40° C. for 2 days. Diethyl ether was added to the reaction mixture, followed by stirring. A supernatant liquid was removed, and solids deposited were collected by filtration and washed with ethanol to obtain the title compound (90 mg) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136823
Source datasetuspto-grants-2000_10
ORD IDord-5bc60a61a04546088e6433649359800b
Source noteuspto-grants-2000_10