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5-FLUOROINDOLE-3-CARBOXYLIC ACID

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5-FLUOROINDOLE-3-CARBOXYLIC ACID Basic information
Application
Product Name:5-FLUOROINDOLE-3-CARBOXYLIC ACID
Synonyms:RARECHEM AL BE 0942;1H-INDOLE-3-CARBOXYLIC ACID,5-FLUORO;5-Fluoro-1H-indol-3-carboxylic acid;5-FLUOROINDOLE-3-CARBOXYLIC ACID;5-fluoro-indol-3-carboxylic acid;5-FLUORO-1H-INDOLE-3-CARBOXYLIC ACID
CAS:23077-43-2
MF:C9H6FNO2
MW:179.15
EINECS:
Product Categories:Indole;pharmacetical
Mol File:23077-43-2.mol
5-FLUOROINDOLE-3-CARBOXYLIC ACID Structure
5-FLUOROINDOLE-3-CARBOXYLIC ACID Chemical Properties
Melting point 234-236 °C (decomp)
Boiling point 422.2±25.0 °C(Predicted)
density 1.510±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka3.76±0.30(Predicted)
AppearanceOff-white to light yellow Solid
Safety Information
HS Code 2933998090
MSDS Information
5-FLUOROINDOLE-3-CARBOXYLIC ACID Usage And Synthesis
Application5-Fluoroindole-3-carboxylic acid can be used as an organic synthesis intermediate and a pharmaceutical intermediate in laboratory research and development processes and in the synthesis of pharmaceutical chemicals.
Synthesis
2,2,2-Trifluoro-1-(5-fluoro-3-indolyl)ethanone

1260793-83-6

5-FLUOROINDOLE-3-CARBOXYLIC ACID

23077-43-2

General procedure for the synthesis of 5-fluoro-1H-indole-3-carboxylic acid from 2,2,2-trifluoro-1-(5-fluoro-1H-indol-3-yl)ethanone: 2,2,2-trifluoro-1-[5-fluoro-1-(pyrimidin-2-yl)-1H-indol-3-yl]ethan-1-one (1.6 g) and 5 N aqueous sodium hydroxide were added to the reaction flask. The reaction mixture was stirred under heated reflux conditions for 1.5 hours. After completion of the reaction, the reaction solution was cooled to room temperature and extracted by adding water and ethyl acetate. After separating the organic and aqueous layers, the aqueous layer was made acidic with concentrated hydrochloric acid. The acidic aqueous layer was again extracted with ethyl acetate, the organic layers were combined and washed with saturated saline. The organic layer was dried with anhydrous sodium sulfate and the solvent was removed by distillation under reduced pressure to give 785 mg of 5-fluoro-1H-indole-3-carboxylic acid (88% yield).

References[1] Journal of Medicinal Chemistry, 2014, vol. 57, # 17, p. 7293 - 7316
[2] Patent: EP2548864, 2013, A1. Location in patent: Paragraph 0178; 0179
[3] Patent: WO2013/14102, 2013, A1. Location in patent: Page/Page column 26; 32; 33
[4] Patent: JP2017/171619, 2017, A. Location in patent: Paragraph 0168; 0170
5-FLUOROINDOLE-3-CARBOXYLIC ACID Preparation Products And Raw materials
Raw materials2,2,2-Trifluoro-1-(5-fluoro-3-indolyl)ethanone-->Trifluoroacetic anhydride-->Carbon dioxide-->Sodium hydroxide-->5-Fluoroindole
Tag:5-FLUOROINDOLE-3-CARBOXYLIC ACID(23077-43-2) Related Product Information
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