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3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE

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3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE Basic information

Product Name:
3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE
Synonyms:
  • 3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE
  • 2-Methoxy-3-Bromo-5-Chloropyridine
  • Pyridine,3-bromo-5-chloro-2-methoxy-
  • oro-2-methoxypyridine
  • 3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE ISO 9001:2015 REACH
  • 2-methoxy-3-bromo-5-clopyridine
CAS:
102830-75-1
MF:
C6H5BrClNO
MW:
222.47
Product Categories:
  • Pyridine Series
  • Boronic Acid
  • Pyridine
  • Indoles ,Indazoles
Mol File:
102830-75-1.mol
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3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE Chemical Properties

Melting point:
49.0 to 53.0 °C
Boiling point:
215.8±35.0 °C(Predicted)
Density 
1.650±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
soluble in Chloroform
form 
powder to crystal
pka
-1.24±0.20(Predicted)
color 
White to Almost white
CAS DataBase Reference
102830-75-1
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Safety Information

Hazard Codes 
T
Risk Statements 
25
Safety Statements 
45
RIDADR 
UN 2811 6.1 / PGIII
HazardClass 
IRRITANT
HS Code 
2933399990
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3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE Usage And Synthesis

Synthesis

13473-01-3

102830-75-1

General procedure for the synthesis of 2-methoxy-3-bromo-5-chloropyridine from 2-methoxy-5-chloropyridine: 1. Glacial acetic acid solution of bromine was prepared by slowly adding bromine (1.5 mL, 29.28 mmol) to glacial acetic acid (7 mL). 2. 5-chloro-2-methoxypyridine (2.1 g, 14.63 mmol) and sodium acetate (1.2 g, 14.63 mmol) were dissolved in glacial acetic acid (7 mL) to form a mixture. 3. The bromine solution prepared in step 1 was slowly added to the mixture in step 2. 4. The resulting reaction mixture was stirred at 80 °C for 6 hours. 5. Upon completion of the reaction, the mixture was allowed to cool to room temperature. 6. Add ether and water to the cooled reaction mixture and extract. 7. The organic layer was separated and washed sequentially with 1N aqueous sodium hydroxide solution and 4% aqueous sodium bisulfite solution. 8. The organic layer was dried with magnesium sulfate and then the solvent was removed under reduced pressure. 9. The residue was purified by fast chromatography (100% hexane as eluent) to afford 2-methoxy-3-bromo-5-chloropyridine (2.1 g, 64% yield) as a white solid. 1H-NMR (300MHz, CDCl3) δ: 3.99 (s, 3H), 7.81 (d, 1H), 8.05 (d, 1H).

References

[1] Journal of Heterocyclic Chemistry, 1985, vol. 22, p. 1583 - 1592
[2] Journal of Medicinal Chemistry, 1986, vol. 29, # 9, p. 1590 - 1595
[3] Patent: WO2012/69202, 2012, A1. Location in patent: Page/Page column 53
[4] Patent: EP2463289, 2012, A1. Location in patent: Page/Page column 21
[5] Patent: US5512575, 1996, A

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