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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyrimidines >  Thiophene pyrimidine >  4-CHLORO-6-METHYLTHIENO[2,3-D]PYRIMIDINE

4-CHLORO-6-METHYLTHIENO[2,3-D]PYRIMIDINE

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4-CHLORO-6-METHYLTHIENO[2,3-D]PYRIMIDINE Basic information

Product Name:
4-CHLORO-6-METHYLTHIENO[2,3-D]PYRIMIDINE
Synonyms:
  • 4-chloro-6-methylthieno[2,3-d]pyrimidine(SALTDATA: FREE)
  • 4-Chloro-6-Methylthieno[2...
  • AKOS 92593
  • 4-CHLORO-6-METHYLTHIENO[2,3-D]PYRIMIDINE
  • Thieno[2,3-d]pyrimidine, 4-chloro-6-methyl-
  • 4-CHLORO-6-METHYLTHIENO[2,3-D]PYRIMIDINE ISO 9001:2015 REACH
CAS:
106691-21-8
MF:
C7H5ClN2S
MW:
184.65
Mol File:
106691-21-8.mol
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4-CHLORO-6-METHYLTHIENO[2,3-D]PYRIMIDINE Chemical Properties

Melting point:
88-91℃ (sublm)
Boiling point:
301.3±37.0 °C(Predicted)
Density 
1.445±0.06 g/cm3 (20 ºC 760 Torr)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
0.56±0.40(Predicted)
Appearance
light yellow solid
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Safety Information

Risk Statements 
36
Safety Statements 
26
WGK Germany 
3
HS Code 
2934999090
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4-CHLORO-6-METHYLTHIENO[2,3-D]PYRIMIDINE Usage And Synthesis

Synthesis

108831-66-9

106691-21-8

GENERAL METHOD: A mixture of 6-methyl-3H-thieno[2,3-d]pyrimidin-4-one (0.01 mol), phosphorus trichloride (11 mL), and phosphorus pentachloride (1.5 g) was rapidly heated to 105°C and the reaction was carried out at reflux for 5-6 hours. After completion of the reaction, excess solvent was removed by distillation under reduced pressure. The crude product was dissolved in dichloromethane (12 mL) and neutralized with cold sodium hydroxide solution (0.5 N). The organic phase was separated, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was recrystallized with isopropanol to afford the target product 4-chloro-6-methylthieno[2,3-d]pyrimidine in 80% yield.

References

[1] Pharmaceutical Chemistry Journal, 1987, vol. 21, # 2, p. 126 - 129
[2] Khimiko-Farmatsevticheskii Zhurnal, 1987, vol. 21, # 2, p. 197 - 200
[3] European Journal of Medicinal Chemistry, 2016, vol. 115, p. 148 - 160
[4] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 2, p. 305 - 308
[5] European Journal of Medicinal Chemistry, 2011, vol. 46, # 3, p. 870 - 876

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