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5-Trifluoromethyl-pyridin-3-ylamine

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5-Trifluoromethyl-pyridin-3-ylamine Basic information

Product Name:
5-Trifluoromethyl-pyridin-3-ylamine
Synonyms:
  • 5-Trifluoromethyl-pyridin-3-ylamine
  • 5-(Trifluoromethyl)-3-pyridinamine
  • 5-(TrifluorMethyl)-3-aMinopyridine
  • 5-(TrifluoroMethyl)pyridin-3-aMine
  • 3-Pyridinamine,5-(trifluoromethyl)
  • 3-Amino-5-trifluoromethyl-pyridine
  • 5-Trifluoromethyl-pyridin-3-ylamine ISO 9001:2015 REACH
CAS:
112110-07-3
MF:
C6H5F3N2
MW:
162.11
Product Categories:
  • Fluorine series
Mol File:
112110-07-3.mol
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5-Trifluoromethyl-pyridin-3-ylamine Chemical Properties

Melting point:
40-41.5 °C
Boiling point:
105.5-106 °C(Press: 11 Torr)
Density 
1.368
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
3.74±0.20(Predicted)
Appearance
Colorless to light yellow <40°C Solid,>41.5°C Liquid
InChI
InChI=1S/C6H5F3N2/c7-6(8,9)4-1-5(10)3-11-2-4/h1-3H,10H2
InChIKey
NJFRBMFEAGFNDC-UHFFFAOYSA-N
SMILES
C1=NC=C(C(F)(F)F)C=C1N
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Safety Information

RIDADR 
UN2811
HS Code 
2933399990
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5-Trifluoromethyl-pyridin-3-ylamine Usage And Synthesis

Synthesis

72587-15-6

112110-07-3

Step Ia: 5-(Trifluoromethyl)-2-chloro-3-nitropyridine (0.850 g, 3.75 mmol) was dissolved in methanol (17 mL), and palladium carbon (800 mg, 10% wetted, 0.375 mmol) was added. The reaction mixture was hydrogenated for 16 h at 60 psi hydrogen pressure and 20 °C. The progress of the reaction was monitored by LCMS to confirm that the starting material (M + H 213/215, 3:1) and hydroxylamine intermediate were completely consumed and a mixture of partially reduced product (M + H 163; UVmax 214, 258, 332 nm) and completely reduced product (M + H 169; no UV absorption) was detected. After completion of the reaction, the reaction mixture was filtered and the filter cake was washed well with methanol. The filtrate was concentrated in vacuum to give 0.74 g of product in the form of HCl salt. Subsequently, the product was purified by preparative HPLC/MS using a 30 mm × 100 mm C18 column; the mobile phase was 20% acetonitrile-water (containing 0.1% NH4OH), with an initial hold of 1 min and a gradient up to 40% over 6 min; the flow rate was 60 mL/min; the detector was set at m/z 163; and the product retention time was 4.4 min. Fractions containing the pure product were collected, combined and concentrated to give 52 mg of the product as an oil in 8% yield.1H NMR (CDCl3) δ 8.26 (s, 1H); 8.24 (d, 1H); 7.15 (t, 1H); 4.00 (s, 2H).

References

[1] Patent: WO2008/79965, 2008, A1. Location in patent: Page/Page column 72-73
[2] Patent: US2006/4018, 2006, A1. Location in patent: Page/Page column 14; 35-36

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