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26893-12-9

26893-12-9 Structure

26893-12-9 Structure
IdentificationBack Directory
[Name]

ETHYL 4-HYDROXY-6-(TRIFLUOROMETHYL)QUINOLINE-3-CARBOXYLATE
[CAS]

26893-12-9
[Synonyms]

BUTTPARK 10\01-32
ETHYL 4-HYDROXY-6-(TRIFLUOROMETHYL)-3-QUINOLINECARBOXYLATE
ETHYL 4-HYDROXY-6-(TRIFLUOROMETHYL)QUINOLINE-3-CARBOXYLATE
ethyl 4-oxo-6-(trifluoromethyl)-1H-quinoline-3-carboxylate
4-HYDROXY-6-TRIFLUOROMETHYLQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER
4-oxo-6-(trifluoromethyl)-1H-quinoline-3-carboxylic acid ethyl ester
3-Quinolinecarboxylic acid, 4-hydroxy-6-(trifluoromethyl)-, ethyl ester
3-(Ethoxycarbonyl)-6-(trifluoromethyl)quinolin-4-ol, 3-(Ethoxycarbonyl)-4-hydroxy-6-(trifluoromethyl)quinoline
[Molecular Formula]

C13H10F3NO3
[MDL Number]

MFCD00173369
[MOL File]

26893-12-9.mol
[Molecular Weight]

285.22
Chemical PropertiesBack Directory
[Melting point ]

336(dec.)
[Boiling point ]

343.5±37.0 °C(Predicted)
[density ]

1.404±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[pka]

1.84±0.50(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280-P301+P312-P261
[Hazard Codes ]

Xi
[Hazard Note ]

Irritant
[HS Code ]

2933499090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

(4-Trifluoromethylphenylamino)methylenemalonic acid diethyl ester
Spectrum DetailBack Directory
[Spectrum Detail]

ETHYL 4-HYDROXY-6-(TRIFLUOROMETHYL)QUINOLINE-3-CARBOXYLATE(26893-12-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

(4-TRIFLUOROMETHYLPHENYLAMINO)METHYLENEMALONIC ACID DIETHYL ESTER

49713-39-5

ETHYL 4-HYDROXY-6-(TRIFLUOROMETHYL)QUINOLINE-3-CARBOXYLATE

26893-12-9

GENERAL METHODS: Polyphosphoric acid (PPA) (2 eq. by weight) was mixed with Intermediate 1 (40 mmol), followed by the addition of phosphoryl chloride (POCl3) (10 mmol). The reaction mixture was heated to 75 °C and maintained for 8 h. The reaction progress was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the mixture was quenched by slowly pouring it into 10% sodium hydroxide solution in an ice bath while adjusting the pH to about 7. The resulting solid was separated by filtration, dried, and washed with ether (3 x 20 mL) to afford ethyl 4-hydroxy-6-trifluoromethylquinoline-3-carboxylate in good yield.

[References]

[1] European Journal of Medicinal Chemistry, 2015, vol. 103, p. 1 - 16
[2] Organic Process Research and Development, 2014, vol. 18, # 11, p. 1482 - 1491
[3] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 6, p. 1577 - 1580
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