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4-METHYLAMINO-2-METHYLSULFANYL-PYRIMIDINE-5-CARBALDEHYDE

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4-METHYLAMINO-2-METHYLSULFANYL-PYRIMIDINE-5-CARBALDEHYDE Basic information

Product Name:
4-METHYLAMINO-2-METHYLSULFANYL-PYRIMIDINE-5-CARBALDEHYDE
Synonyms:
  • 4-METHYLAMINO-2-METHYLSULFANYL-PYRIMIDINE-5-CARBALDEHYDE
  • 4-(Methylamino)-2-(methylthio)pyrimidine-5-carbaldehyde
  • 4-(Methylamino)-2-(methylthio)pyrimidine-5-carboxaldehyde
  • 5-Pyrimidinecarboxaldehyde, 4-(methylamino)-2-(methylthio)-
  • 4-MethylaMino-2-Methanesulfanyl-pyriMidine-5-carboxaldehyde
  • 4-MethylaMino-2-MethylsulfanylpyriMidine
  • 4-(MethylaMino)-2-(Met hylsulfanyl)pyriMidine-5-carboxaldehyde
  • 4-(MethylaMino)-2-(Methylthio)-5-pyriMidinecarboxaldehyde
CAS:
185040-32-8
MF:
C7H9N3OS
MW:
183.23
Product Categories:
  • Building Blocks
  • Pyrimidine
  • Amines
  • Aromatics
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Sulfur & Selenium Compounds
  • Heterocycle-Pyrimidine series
Mol File:
185040-32-8.mol
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4-METHYLAMINO-2-METHYLSULFANYL-PYRIMIDINE-5-CARBALDEHYDE Chemical Properties

Melting point:
99-101 °C
Boiling point:
377.1±27.0 °C(Predicted)
Density 
1.27±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
solubility 
Chloroform, Dichloromethane, DMSO, Ethyl Acetate, Methanol
form 
Solid
pka
3.15±0.10(Predicted)
color 
White
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4-METHYLAMINO-2-METHYLSULFANYL-PYRIMIDINE-5-CARBALDEHYDE Usage And Synthesis

Chemical Properties

White Solid

Uses

Intermediate in the preparation of p38 kinase inhibitors

Synthesis

17759-30-7

185040-32-8

In a dry 3L three-necked round-bottomed flask equipped with an overhead mechanical stirrer and an argon inlet, 32.74 g (176.7 mmol) of (4-methylamino-2-methanesulfonyl-pyrimidin-5-yl)-methanol was dissolved in 1.6 L of chloroform. Under stirring conditions, 152 g (1.75 mol) of manganese dioxide was added in batches. The reaction mixture was slightly heated and stirred continuously for 7 hours. Upon completion of the reaction, vacuum filtration was performed through a diatomaceous earth pad to remove the manganese dioxide and the filter cake was washed well with two 300mL portions of chloroform. The filtrates were combined and concentrated to give a white solid product. After vacuum drying, 30.6 g (94% yield) of 4-methylamino-2-methylthio-5-formylpyrimidine was obtained. The spectral data of the obtained product were in agreement with the values reported in the literature.

References

[1] Patent: WO2004/63195, 2004, A1. Location in patent: Page 53-54
[2] Journal of Medicinal Chemistry, 1998, vol. 41, # 17, p. 3276 - 3292
[3] Patent: WO2006/71940, 2006, A2. Location in patent: Page/Page column 355
[4] Patent: WO2008/33999, 2008, A2. Location in patent: Page/Page column 88
[5] Patent: WO2014/11900, 2014, A2. Location in patent: Page/Page column 31; 32

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