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2,3-DICHLORO-5-FORMYLPYRIDINE

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2,3-DICHLORO-5-FORMYLPYRIDINE Basic information

Product Name:
2,3-DICHLORO-5-FORMYLPYRIDINE
Synonyms:
  • 2,3-DICHLORO-5-FORMYLPYRIDINE
  • 5,6-DICHLOROPYRIDINE-3-CARBALDEHYDE
  • 5,6-Dichloropyridine-3-carboxaldehyde
  • 5,6-Dichloro-3-pyridinecarboxaldehyde
  • 5,6-Dichloropyridyl-3-carboxaldehyde
  • 3-Pyridinecarboxaldehyde, 5,6-dichloro-
  • 2,3-DICHLORO-5-FORMYLPYRIDINE ISO 9001:2015 REACH
CAS:
71690-05-6
MF:
C6H3Cl2NO
MW:
176
Product Categories:
  • Heterocycle-Pyridine series
  • Boronic Acid
  • Pyridine
Mol File:
71690-05-6.mol
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2,3-DICHLORO-5-FORMYLPYRIDINE Chemical Properties

storage temp. 
Inert atmosphere,2-8°C
Appearance
Off-white to light yellow Solid
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933399990
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2,3-DICHLORO-5-FORMYLPYRIDINE Usage And Synthesis

Uses

5,6-Dichloropyridyl-3-carboxaldehyde is used to prepare [(pyridyl)piperazinyl]benzimidazoles analogs as potent, orally available antagonists of the transient receptor potential vanilloid 1 and analgesics. It is also used to synthesize heterocyclic aryl isoxazolines with insecticidal activities.

Synthesis

54127-30-9

71690-05-6

General procedure for the synthesis of 2,3-dichloro-5-formylpyridine from 5,6-dichloro-3-pyrimidinemethanol: To a 500 mL round-bottomed flask was added an anhydrous dichloromethane (150 mL) solution of 2,3-dichloro-5-hydroxymethylpyridine (64.810 g, 50.0 mmol), followed by manganese oxide (43.5 g, 0.50 mol). The reaction mixture was stirred at 25 °C for 48 hours. Upon completion of the reaction, it was filtered through Celite and the filtrate was concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography using ethyl acetate (0%-40%)/hexane gradient elution to afford 2,3-dichloro-5-formylpyridine (7.2 g, 90% yield). The product was confirmed by 1H NMR (400 MHz, CDCl3): δ10.08 (1H, s), 8.77 (1H, d, J=1.97 Hz), 8.25 (1H, d, J=1.97 Hz). the LC/MS analysis showed the molecular ion peak (M+1) was 176.

References

[1] Patent: US2010/120862, 2010, A1. Location in patent: Page/Page column 94
[2] Patent: US2010/137306, 2010, A1. Location in patent: Page/Page column 169
[3] Patent: US2010/130499, 2010, A1. Location in patent: Page/Page column 122
[4] Patent: WO2008/132600, 2008, A2. Location in patent: Page/Page column 258
[5] Patent: WO2008/133973, 2008, A1. Location in patent: Page/Page column 68-69

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