ChemicalBook > Product Catalog >Pharmaceutical intermediates >Heterocyclic compound >Pyrimidines >Bromopyrimidine >4-Bromo-2-(methylsulfonyl)pyrimidine

4-Bromo-2-(methylsulfonyl)pyrimidine

4-Bromo-2-(methylsulfonyl)pyrimidine Suppliers list
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4-Bromo-2-(methylsulfonyl)pyrimidine manufacturers

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
EINECS:
Product Categories:Heterocycle-Pyrimidine series
Mol File:1208538-52-6.mol
4-Bromo-2-(methylsulfonyl)pyrimidine Structure
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)
AppearanceOff-white to light yellow Solid
Safety Information
MSDS Information
4-Bromo-2-(methylsulfonyl)pyrimidine Usage And Synthesis
Synthesis
2-METHYLTHIO-4-BROMOPYRIMIDINE

959236-97-6

4-Bromo-2-(methylsulfonyl)pyrimidine

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
4-Bromo-2-(methylsulfonyl)pyrimidine Preparation Products And Raw materials
Raw materials2-Methylthio-4-bromopyrimidine
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