5-Amino-2-fluoropyridine
5-Amino-2-fluoropyridine Basic information
- Product Name:
- 5-Amino-2-fluoropyridine
- Synonyms:
-
- 2-FLUORO-5-AMINO PYRIDINE
- 6-FLUORO-3-PYRIDINAMINE
- 6-FLUOROPYRIDIN-3-AMINE
- 6-FLUORO-PYRIDIN-3-YLAMINE
- 5-AMINO-2-FLUOROPYRIDINE
- 2-FLUOROPYRIDIN-5-AMINE
- 5-Amino-2-fluoropyridine 98%
- 5-Amino-2-fluoropyridine98%
- CAS:
- 1827-27-6
- MF:
- C5H5FN2
- MW:
- 112.11
- EINECS:
- 675-011-2
- Product Categories:
-
- Pyridine
- pharmacetical
- Pyridine series
- Pyridines
- Boronic Acid
- Fluorin-contained pyridine series
- Fluorine series
- Building Blocks
- C5
- C5 to C6
- Chemical Synthesis
- Fluorinated Building Blocks
- Halogenated Heterocycles
- Heterocyclic Building Blocks
- Heterocyclic Fluorinated Building Blocks
- Other Fluorinated Heterocycles
- Mol File:
- 1827-27-6.mol
5-Amino-2-fluoropyridine Chemical Properties
- Melting point:
- 86-87°C
- Boiling point:
- 264.0±20.0 °C(Predicted)
- Density
- 1.257±0.06 g/cm3(Predicted)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- pka
- 2?+-.0.10(Predicted)
- form
- powder to crystal
- color
- Purple to Dark purple to Dark red
- CAS DataBase Reference
- 1827-27-6(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38-41-37/38
- Safety Statements
- 26-36/37/39
- WGK Germany
- 3
- Hazard Note
- Irritant
- HazardClass
- 6.1
- HS Code
- 29333990
5-Amino-2-fluoropyridine Usage And Synthesis
Chemical Properties
Light yellow Cryst
Uses
5-Amino-2-fluoropyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Synthesis
456-24-6
1827-27-6
General procedure for the synthesis of 2-fluoro-5-aminopyridine from 2-fluoro-5-nitropyridine: 50 mL of toluene and 50 mmol of 2-fluoro-5-nitropyridine were added to a 100 mL round-bottomed flask, followed by 0.282 g of 5% Pd/C catalyst and 10 mmol of anhydrous sodium sulfate. The reaction system was placed under hydrogen atmosphere, heated and stirred for 15 hours. Upon completion of the reaction, the mixture was cooled to room temperature, the catalyst was removed by filtration and the filtrate was concentrated by rotary evaporation. The resulting crude product was purified by recrystallization and finally dried under vacuum to give 1.6806 g of 2-fluoro-5-aminopyridine solid in 75% yield.
References
[1] Journal of the Chemical Society - Perkin Transactions 1, 1996, # 18, p. 2221 - 2226
[2] Patent: CN103755744, 2016, B. Location in patent: Paragraph 0065; 0066
[3] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 6, p. 1411 - 1416
[4] Patent: US6355636, 2002, B1. Location in patent: Page column 64
[5] Patent: EP1171440, 2004, B1. Location in patent: Page 53
5-Amino-2-fluoropyridine Preparation Products And Raw materials
Preparation Products
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