ChemicalBook--->CAS DataBase List--->127199-27-3

127199-27-3

127199-27-3 Structure

127199-27-3 Structure
IdentificationBack Directory
[Name]

3-Quinolinecarboxylic acid, 8-chloro-6,7-difluoro-1-[(1R,2S)-2-fluorocyclopropyl]-1,4-dihydro-4-oxo-
[CAS]

127199-27-3
[Synonyms]

Sitafloxacin Impurity 63
8-Chloro-6,7-difluoro-1-((1R,2S)-2-fluorocyclopropyl)--4-oxo-1,4-dihydroquinoline-3-carboxylic
8-Chloro-6,7-difluoro-1-[(1R,2S)-2-fluorocyclopropyl]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
8-chloro-6,7-difluoro-1-((1R,2S)-2-fluorocyclopropyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
(1R-cis)-8-Chloro-6,7-difluoro-1-(2-fluorocyclopropyl)-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
3-Quinolinecarboxylic acid, 8-chloro-6,7-difluoro-1-[(1R,2S)-2-fluorocyclopropyl]-1,4-dihydro-4-oxo-
[EINECS(EC#)]

1312995-182-4
[Molecular Formula]

C13H7ClF3NO3
[MDL Number]

MFCD23701744
[MOL File]

127199-27-3.mol
[Molecular Weight]

317.65
Chemical PropertiesBack Directory
[Boiling point ]

475.6±45.0 °C(Predicted)
[density ]

1.71
[storage temp. ]

2-8°C
[pka]

6.33±0.50(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
Hazard InformationBack Directory
[Synthesis]

3-Quinolinecarboxylic acid, 8-chloro-6,7-difluoro-1-(2-fluorocyclopropyl)-1,4-dihydro-4-oxo-,ethyl ester

127199-25-1

3-Quinolinecarboxylic acid, 8-chloro-6,7-difluoro-1-[(1R,2S)-2-fluorocyclopropyl]-1,4-dihydro-4-oxo-

127199-27-3

Ethyl 8-chloro-6,7-difluoro-1-((1R,2S)-2-fluorocyclopropyl)-4-ethyl-1,4-dihydroquinoline-3-carboxylate (Compound 3, 12.4 g, 34.3 mmol) was used as raw material. Compound 3 was dissolved in a mixture of hydrochloric acid (125 mL) and acetic acid (125 mL). The reaction mixture was stirred at 120-130°C for 2 hours. After completion of the reaction, the reaction solution was diluted with deionized water (500 mL) and the precipitate was collected by filtration. The precipitate was washed sequentially with deionized water and ether and then dried under reduced pressure to afford the target product 8-chloro-6,7-difluoro-1-((1R,2S)-2-fluorocyclopropyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (Compound 4, 8.72 g, 76.2% yield) as a colorless solid.

[References]

[1] Journal of Medicinal Chemistry, 1994, vol. 37, # 20, p. 3344 - 3352
[2] Asian Journal of Chemistry, 2014, vol. 26, # 20, p. 7049 - 7051
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