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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyrimidines >  Chloropyrimidine >  ETHYL 2-CHLORO-4-METHYLPYRIMIDINE-5-CARBOXYLATE

ETHYL 2-CHLORO-4-METHYLPYRIMIDINE-5-CARBOXYLATE

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ETHYL 2-CHLORO-4-METHYLPYRIMIDINE-5-CARBOXYLATE Basic information

Product Name:
ETHYL 2-CHLORO-4-METHYLPYRIMIDINE-5-CARBOXYLATE
Synonyms:
  • ETHYL 2-CHLORO-4-METHYLPYRIMIDINE-5-CARBOXYLATE
  • 2-Chloro-5-(ethoxycarbonyl)-4-methylpyrimidine
  • 2-Chloro-4-methyl-5-pyrimidinecarboxylic acid ethyl ester
  • Ethyl 2-chloro-4-methylpyrimidine-5-carboxylate ,97%
  • 2-Chloro-5-(ethoxycarbonyl)-4-methylpyrimidine, 2-Chloro-5-(ethoxycarbonyl)-4-methyl-1,3-diazine
  • 5-Pyrimidinecarboxylic acid, 2-chloro-4-methyl-, ethyl ester
  • 5-Pyrimidinecarboxylic acid, 2-chloro-4-methyl-, ethyl ester (9CI, ACI)
  • 2-chloro-4-methyl-5-Pyrimidinecarboxylic acid ethyl ester (9CI ACI)
CAS:
188781-08-0
MF:
C8H9ClN2O2
MW:
200.62
Product Categories:
  • pyrimidine
  • Heterocycle-Pyrimidine series
Mol File:
Mol File
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ETHYL 2-CHLORO-4-METHYLPYRIMIDINE-5-CARBOXYLATE Chemical Properties

Boiling point:
302.7±22.0 °C(Predicted)
Density 
1.265
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
solid
pka
-2.56±0.29(Predicted)
color 
white
Water Solubility 
Slightly soluble in water.
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HS Code 
29335990
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ETHYL 2-CHLORO-4-METHYLPYRIMIDINE-5-CARBOXYLATE Usage And Synthesis

Chemical Properties

White solid

Uses

It is an active pharmaceutical intermediates.

Synthesis

6214-64-8

188781-08-0

The general procedure for the synthesis of ethyl 4-methyl-2-chloropyrimidine-5-carboxylate from ethyl 4-methyl-2-hydroxypyrimidine-5-carboxylate was as follows: ethyl 4-methyl-2-hydroxypyrimidine-5-carboxylate (10 mmol) was dissolved in phosphorochloride (10 mL), and heated and refluxed for 30 min. Upon completion of the reaction, the excess phosphorus trichloride was removed by distillation under reduced pressure. Subsequently, residual phosphorous trichloride was removed by azeotropic distillation with dried benzene. Finally, the crude product was purified by column chromatography to afford pure ethyl 4-methyl-2-chloropyrimidine-5-carboxylate.

References

[1] European Journal of Medicinal Chemistry, 2011, vol. 46, # 6, p. 2290 - 2294
[2] Patent: WO2016/37578, 2016, A1. Location in patent: Page/Page column 70
[3] European Journal of Medicinal Chemistry, 2013, vol. 66, p. 314 - 323

ETHYL 2-CHLORO-4-METHYLPYRIMIDINE-5-CARBOXYLATE Preparation Products And Raw materials

Raw materials

ETHYL 2-CHLORO-4-METHYLPYRIMIDINE-5-CARBOXYLATESupplier

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