4-METHYLAMINO-2-METHYLSULFANYL-PYRIMIDINE-5-CARBALDEHYDE
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
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
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
4-METHYLAMINO-2-METHYLSULFANYL-PYRIMIDINE-5-CARBALDEHYDESupplier
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4-METHYLAMINO-2-METHYLSULFANYL-PYRIMIDINE-5-CARBALDEHYDE(185040-32-8)Related Product Information
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