Basic information Application Safety Supplier Related

2-FLUORO-3-PYRIDINEMETHANAMINE

Basic information Application Safety Supplier Related

2-FLUORO-3-PYRIDINEMETHANAMINE Basic information

Product Name:
2-FLUORO-3-PYRIDINEMETHANAMINE
Synonyms:
  • (2-Fluoropyridin-3-yl)MethanaMine hydrochloride
  • 2-Fluoro-3-pyridinemethanamine,hydrochloride
  • (2-Fluoropyridin-3-yl)methanamine dihydrochloride
  • 2-fluoro-3-(aminomethyl)pyridine hydrochloride
  • RARECHEM AL BW 2476
  • 2-FLUORO-3-PYRIDINEMETHANAMINE
  • (2-FLUOROPYRIDIN-3-YL)METHANAMINE
  • 2-fluoro-3-pyridineMethanaMine dihydrochloride
CAS:
859164-64-0
MF:
C6H7FN2
MW:
126.13
Mol File:
859164-64-0.mol
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2-FLUORO-3-PYRIDINEMETHANAMINE Chemical Properties

storage temp. 
Inert atmosphere,Room Temperature
Appearance
White to off-white Solid
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2-FLUORO-3-PYRIDINEMETHANAMINE Usage And Synthesis

Application

2-Fluoro-3-pyridinemethylmethylamine is an amine organic compound that can be used as a pharmaceutical synthesis intermediate.

Synthesis

3939-13-7

859164-64-0

General procedure for the synthesis of 2-fluoro-3-pyridinylmethylamine from 2-fluoro-3-cyanopyridine: first, C-(2-fluoro-pyridin-3-yl)-methylamine hydrochloride was prepared. Concentrated hydrochloric acid (0.46 mL) was slowly added to a suspension of methanol (10 mL) containing 2-fluoro-3-cyanopyridine (0.34 g, 2.8 mmol) and 5% Pd/C (0.5 g) at room temperature. Subsequently, the reaction suspension was stirred continuously for 6 hours under a hydrogen atmosphere at 1 atmosphere. Upon completion of the reaction, the reaction mixture was filtered and the filtrate concentrated. Ether was added to the concentrated residue and HCl gas was passed through the suspension bulge. The resulting precipitate was filtered and dried to give the target product 2-fluoro-3-pyridylmethylmethylamine (0.37 g, 82% yield). Substance spectral analysis (ES) of the product showed a m/z of 127.1 ([M + H]+). The NMR hydrogen spectrum (400 MHz, DMSO-d6) data were as follows: δ 8.65 (broad single peak, 3H), 8.24 (multiple peaks, 1H), 8.16 (multiple peaks, 1H), 7.41 (multiple peaks, 1H), 4.06 (multiple peaks, 2H).

References

[1] Patent: WO2005/66126, 2005, A1. Location in patent: Page/Page column 59

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