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4-Bromo-2-(methylsulfonyl)pyrimidine

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4-Bromo-2-(methylsulfonyl)pyrimidine Basic information

Product Name:
4-Bromo-2-(methylsulfonyl)pyrimidine
Synonyms:
  • 4-Bromo-2-(methylsulfonyl)pyrimidine
  • 4-Bromo-2-(methylsulfonyl)
  • Pyrimidine, 4-bromo-2-(methylsulfonyl)-
  • 4-Bromo-2-(methylsulfonyl)pyrimidine ISO 9001:2015 REACH
CAS:
1208538-52-6
MF:
C5H5BrN2O2S
MW:
237.07
Product Categories:
  • Heterocycle-Pyrimidine series
Mol File:
1208538-52-6.mol
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4-Bromo-2-(methylsulfonyl)pyrimidine Chemical Properties

Melting point:
111-112 °C
Boiling point:
393.7±34.0 °C(Predicted)
Density 
1.771±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-4.97±0.20(Predicted)
Appearance
Off-white to light yellow Solid
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4-Bromo-2-(methylsulfonyl)pyrimidine Usage And Synthesis

Synthesis

959236-97-6

1208538-52-6

General procedure for the synthesis of 4-bromo-2-(methylthio)pyrimidine from 2-methylthio-4-bromopyrimidine: ammonium molybdate tetrahydrate (1.09 g, 0.88 mmol, 0.03 eq.) was added in batches to a stirred solution of 30% H2O2 (6 g, 29.4 mmol, 1 eq.) at 0 °C for 20 min. Subsequently, a solution of 4-bromo-2-(methylthio)pyrimidine (6 g, 29.41 mmol, 1 eq.) was slowly added, keeping the reaction temperature at 0 °C. After addition, the reaction mixture was brought to room temperature and stirred for 3 hours. The reaction progress was monitored by TLC. Upon completion of the reaction, the reaction mixture was concentrated to a crude residue, diluted with cold water and then extracted with dichloromethane (DCM, 3 x 100 mL). The organic layers were combined, washed sequentially with 5% H2SO4 solution and water, dried over anhydrous Na2SO4 and concentrated to give the crude product. The crude product was purified by silica gel column chromatography (100-200 mesh) with the eluent being a petroleum ether solution of 0-40% ethyl acetate, resulting in 4-bromo-2-(methylsulfonyl)pyrimidine (6 g, 86% yield) as an off-white solid.LCMS: [M + H]+ 238.84.

References

[1] ChemMedChem, 2016, vol. 11, # 22, p. 2522 - 2533
[2] Organic Letters, 2011, vol. 13, # 19, p. 5000 - 5003
[3] Patent: WO2017/147700, 2017, A1. Location in patent: Paragraph 001095

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