Basic information Safety Supplier Related

5-bromo-3-ethynylpyrazin-2-amine

Basic information Safety Supplier Related

5-bromo-3-ethynylpyrazin-2-amine Basic information

Product Name:
5-bromo-3-ethynylpyrazin-2-amine
Synonyms:
  • 5-BroMo-3-ethynyl-pyrazin-2-ylaMine
  • 2-Pyrazinamine, 5-bromo-3-ethynyl-
  • 5-Bromo-3-ethynyl-2-pyrazinamine
  • 5-bromo-3-ethynylpyrazin-2-amine
  • EOS-61574
  • 2-Amino-5-bromo-3-ethynylpyrazine - [A42148]
CAS:
1209289-08-6
MF:
C6H4BrN3
MW:
198.02
Mol File:
1209289-08-6.mol
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5-bromo-3-ethynylpyrazin-2-amine Chemical Properties

Boiling point:
313.7±42.0 °C(Predicted)
Density 
1.80±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
0.92±0.10(Predicted)
Appearance
Light yellow to yellow Solid
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Safety Information

HS Code 
2933998090
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5-bromo-3-ethynylpyrazin-2-amine Usage And Synthesis

Synthesis

875781-41-2

1209289-08-6

Step 2: Synthesis of 5-bromo-3-ethynylpyrazin-2-amine A solution of 5-bromo-3-[(trimethylsilyl)alkynyl]pyrazin-2-amine (2.5 g, 9.25 mmol) and potassium carbonate (1.279 g, 9.25 mmol) in methanol (40 mL) was added to a 150 mL round-bottomed flask, and the reaction mixture was brown in color. The reaction was stirred at room temperature for 30 minutes. After completion of the reaction, the mixture was extracted with dichloromethane and the organic layer was washed sequentially with water and brine. The organic layer was separated, dried with anhydrous magnesium sulfate, filtered and the solvent was concentrated under reduced pressure to give a brown solid product (1.54 g). Product Characterization: LCMS: retention time 0.78 min, mass-to-charge ratio m/z 200.2 [M + H]+; analytical method: 2 min low pH method. 1H NMR (400 MHz, DMSO-d6) δ 8.12 (1H, s), 6.86 (2H, br s), 4.81 (1H, s).

References

[1] Patent: WO2015/162459, 2015, A1. Location in patent: Page/Page column 328

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