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4-Chloro-6-methoxy-2-(methylthio)pyrimidine

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4-Chloro-6-methoxy-2-(methylthio)pyrimidine Basic information

Product Name:
4-Chloro-6-methoxy-2-(methylthio)pyrimidine
Synonyms:
  • 4-Chloro-6-methoxy-2-(methylthio)pyrimidine ,98%
  • 4-CHLORO-6-METHOXY-2-(METHYLTHIO)PYRIMIDINE
  • 4-Chloro-6-methoxy-2-(methylthio)
  • Pyrimidine, 4-chloro-6-methoxy-2-(methylthio)-
  • 6-methoxy-2-methylthio-4-chlorpyrimidine
CAS:
89466-42-2
MF:
C6H7ClN2OS
MW:
190.65
EINECS:
604-604-1
Mol File:
89466-42-2.mol
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4-Chloro-6-methoxy-2-(methylthio)pyrimidine Chemical Properties

Melting point:
38-39℃
Boiling point:
288℃
Density 
1.36
refractive index 
1.
Flash point:
128℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-2.26±0.30(Predicted)
Appearance
white solid
InChI
InChI=1S/C6H7ClN2OS/c1-10-5-3-4(7)8-6(9-5)11-2/h3H,1-2H3
InChIKey
FNYLFWGITLMOHA-UHFFFAOYSA-N
SMILES
C1(SC)=NC(OC)=CC(Cl)=N1
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Safety Information

Risk Statements 
22
Safety Statements 
36/37
HS Code 
29335990
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4-Chloro-6-methoxy-2-(methylthio)pyrimidine Usage And Synthesis

Chemical Properties

White solid

Uses

4-chloro-6-methoxy-2-(methylthio)pyrimidine is a versatile scaffold and can undergo Suzuki-Miyaura coupling to afford 4-aryl-6-methoxy-2-(methylthio)pyrimidines, as well as amine or alcohol displacement of the chloride, oxidation to sulfone, and condensation reactions to give polycyclic systems][1].

Synthesis

67-56-1

6299-25-8

89466-42-2

To a reaction vial containing an ethanol solution (20 mL) of sodium (0.28 g, 12 mmol) was added 4,6-dichloro-2-(methylthio)pyrimidine (1.95 g, 10 mmol) and stirred at room temperature until the reaction was complete, the progress of the reaction was monitored by thin layer chromatography (TLC). After completion of the reaction, the solvent was removed by evaporation under reduced pressure and quenched by addition of water. Subsequently extracted with dichloromethane (CH2Cl2), the organic phase was washed with water and dried with anhydrous sodium sulfate (Na2SO4). The organic phase was concentrated under reduced pressure and the residue was recrystallized with ether to afford the target compound 6-methoxy-2-methylthio-4-chloropyrimidine (4 g) as a white solid in 70% yield with a melting point of 39-40°C. IR spectra (KBr, cm-1 ): 3003, 2939, 1544, 1328, 1274, 1505, 1030, 820. NMR hydrogen spectra ( 1H NMR, 400 MHz, CDCl3) δ: 2.55 (s, 3H, SCH3), 3.97 (s, 3H, OCH3), 6.41 (s, 1H, pyrimidine-H). Nuclear magnetic resonance carbon spectrum (13C NMR, 100 MHz, CDCl3): δ14.29, 54.52, 102.43, 160.34, 169.90, 172.92. liquid chromatography-mass spectrometry (LC-MS, m/z): 190.0. calculated elemental analysis values (C6H7ClN2OS): C, 37.80; H, 3.70; N 14.69. Measured values: C, 37.72; H, 3.75; N, 14.78.

References

[1] A. Kalogirou, P. Koutentis. “4-Chloro-6-ethoxy-2-(methylthio)pyrimidine.” Molbank 2017 1 (2016).

4-Chloro-6-methoxy-2-(methylthio)pyrimidine Preparation Products And Raw materials

Raw materials

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