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DIETHYL 4-CHLORO-2,6-PYRIDINEDICARBOXYLATE

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DIETHYL 4-CHLORO-2,6-PYRIDINEDICARBOXYLATE Basic information

Product Name:
DIETHYL 4-CHLORO-2,6-PYRIDINEDICARBOXYLATE
Synonyms:
  • DIETHYL 4-CHLORO-2,6-PYRIDINEDICARBOXYLATE
  • DIETHYL 4-CHLOROPYRIDINE-2,6-DICARBOXYLATE
  • 4-Chloro-2,6-pyridinedicarboxylic acid diethyl ester
  • Diethyl 4-Chloropyridine- 2,6-pyridinedicarboxylate
  • 4-chloropyridine-2,6-dicarboxylate
  • 4-Chloro-2,6-(diethoxycarbonyl)pyridine
  • 4-chloropyidine-2,6-dicarboxylate
  • Ethyl 4-chloropyidine-2,6-dicarboxylate
CAS:
53389-01-8
MF:
C11H12ClNO4
MW:
257.67
Product Categories:
  • Pyridines
  • Esters
Mol File:
53389-01-8.mol
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DIETHYL 4-CHLORO-2,6-PYRIDINEDICARBOXYLATE Chemical Properties

Melting point:
91-93°
Boiling point:
378.5±37.0 °C(Predicted)
Density 
1.266
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
-2.14±0.10(Predicted)
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2933399990
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DIETHYL 4-CHLORO-2,6-PYRIDINEDICARBOXYLATE Usage And Synthesis

Uses

Diethyl 4-Chloropyridine-2,6-dicarboxylate is a chemical reagent used in the synthesis of luminescent lanthanide complexes. Also used in the production of metal chelating inhibitors against fructose 1,6-bisphosphate (FBP) aldolase in the treatment of infectious bacteria and fungi.

Synthesis

71022-75-8

64-17-5

53389-01-8

The crude 4-chloropyridine-2,6-dicarbonyl dichloride was dissolved in dichloromethane (100 mL) under cooling conditions in an ice bath, followed by the slow addition of a mixture of pyridine (6 mL) and ethanol (5 mL). The reaction mixture was stirred in an ice bath for 5 minutes, then removed from the ice bath and continued to stir at room temperature for 5 hours. Upon completion of the reaction, the volatile solvent was removed by distillation under reduced pressure. The residue was washed with a mixture of 1 M hydrochloric acid (30 mL) and saturated aqueous sodium chloride solution (50 mL) and subsequently extracted with dichloromethane (200 mL). The organic phases were combined, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel fast column chromatography using ethyl acetate-hexane (1:4, subsequently adjusted to 1:3) as eluent to give finally diethyl 4-chloro-2,6-pyridinedicarboxylate (800 mg, 62% yield). The product was characterized by 1H NMR (DMSO-d6): δ 1.36 (t, 6H, J = 7.1 Hz, CH3), 3.33 (s, 3H, CH3), 4.40 (q, 4H, J = 7.1 Hz, CH2), 8.31 (s, 2H, Ar).

References

[1] Patent: US2004/198728, 2004, A1. Location in patent: Page/Page column 8
[2] Canadian Journal of Chemistry, 1991, vol. 69, # 7, p. 1107 - 1116
[3] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 21, p. 4703 - 4707
[4] Chemical Communications, 2014, vol. 50, # 71, p. 10323 - 10326

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