5-Trifluoromethyl-pyridin-3-ylamine
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
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
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
5-Trifluoromethyl-pyridin-3-ylamineSupplier
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5-Trifluoromethyl-pyridin-3-ylamine(112110-07-3)Related Product Information
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- 3-PHENYL-8-(TRIFLUOROMETHYL)PYRIDO[2,3-E][1,2,3]TRIAZOLO[1,5-A]PYRIMIDIN-5-AMINE
- 5-AMINO-8-(TRIFLUOROMETHYL)PYRIDO[2,3-E][1,2,3]TRIAZOLO[1,5-A]PYRIMIDINE-3-CARBOXAMIDE
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- 5-AMINO-8-(TRIFLUOROMETHYL)PYRIDO[2,3-E][1,2,3]TRIAZOLO[1,5-A]PYRIMIDINE-3-CARBONITRILE
- (4-CHLOROPHENYL)[3-(DIMETHYLAMINO)-5-(TRIFLUOROMETHYL)-2-PYRIDINYL]METHANONE