Basic information Uses Safety Supplier Related
ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyrimidines >  Thio pyrimidine >  2-CHLORO-4-METHYLSULFANYL-PYRIMIDINE

2-CHLORO-4-METHYLSULFANYL-PYRIMIDINE

Basic information Uses Safety Supplier Related

2-CHLORO-4-METHYLSULFANYL-PYRIMIDINE Basic information

Product Name:
2-CHLORO-4-METHYLSULFANYL-PYRIMIDINE
Synonyms:
  • 2-CHLORO-4-METHYLSULFANYL-PYRIMIDINE
  • 2-Chloro-4-(methylsulphanyl)pyrimidine, 2-Chloro-4-(methylsulphonyl)-1,3-diazine
  • Pyrimidine, 2-chloro-4-(methylthio)-
  • 2-CHLORO-4-METHYLSULFANYL-PYRIMIDINE ISO 9001:2015 REACH
CAS:
49844-93-1
MF:
C5H5ClN2S
MW:
160.62
Product Categories:
  • Building Blocks
  • Pyrimidine
  • Heterocycle-Pyrimidine series
Mol File:
49844-93-1.mol
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2-CHLORO-4-METHYLSULFANYL-PYRIMIDINE Chemical Properties

Melting point:
67-68 °C
Boiling point:
125-126 °C(Press: 15 Torr)
Density 
1.37±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
-0.45±0.20(Predicted)
color 
white
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HS Code 
29335990
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2-CHLORO-4-METHYLSULFANYL-PYRIMIDINE Usage And Synthesis

Uses

2-Chloro-4-methylthiopyrimidine can be used as a pharmaceutical synthesis intermediate.

Synthesis

3934-20-1

5188-07-8

49844-93-1

At -10 °C, 2,4-dichloropyrimidine (20.0 g, 0.13 mol) was dissolved in 150 mL of anhydrous tetrahydrofuran, and sodium methanethiol (49.30 mL, 0.15 mol) was added slowly. The reaction mixture was gradually warmed up to room temperature with continuous stirring for 5 h, during which the reaction progress was monitored by liquid chromatography-mass spectrometry (LC-MS) or thin-layer chromatography (TLC). Upon completion of the reaction, the reaction mixture was diluted with ethyl acetate and washed twice with saturated saline (x2). The organic layers were combined, dried with anhydrous sodium sulfate and subsequently concentrated under reduced pressure. The resulting solid was recrystallized with ether and collected by filtration to afford the target product 2-chloro-4-methylthiopyrimidine (Intermediate 10) as a white solid (11.2 g, 52% yield).

References

[1] Journal of Heterocyclic Chemistry, 2007, vol. 44, # 4, p. 967 - 971
[2] Organic Letters, 2016, vol. 18, # 9, p. 2180 - 2183
[3] Patent: WO2013/109882, 2013, A1. Location in patent: Page/Page column 63
[4] Patent: US2016/83365, 2016, A1. Location in patent: Paragraph 0841-0843
[5] Journal of Organic Chemistry, 2017, vol. 82, # 5, p. 2664 - 2671

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