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5-BROMO-2-ISOPROPOXYPYRIDINE

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5-BROMO-2-ISOPROPOXYPYRIDINE Basic information

Product Name:
5-BROMO-2-ISOPROPOXYPYRIDINE
Synonyms:
  • 5-BroMo-2-isopropyloxypyridine
  • 5-broMo-2-(propan-2-yloxy)pyridine
  • 5-BroMo-2-isopropylpyridine
  • 5-BROMO-2-ISOPROPOXYPYRIDINE
  • 3-Bromo-6-(i-propoxy)pyridine
  • Pyridine, 5-bromo-2-(1-methylethoxy)-
  • 5-BROMO-2-ISOPROPOXYPYRIDINE ISO 9001:2015 REACH
CAS:
870521-31-6
MF:
C8H10BrNO
MW:
216.08
Product Categories:
  • alkyl bromide
  • Pyridine Series
  • Boronic Acid
Mol File:
870521-31-6.mol
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5-BROMO-2-ISOPROPOXYPYRIDINE Chemical Properties

Boiling point:
228.3±20.0 °C(Predicted)
Density 
1.383±0.06 g/cm3(Predicted)
refractive index 
1.5305
storage temp. 
Inert atmosphere,Room Temperature
pka
1.88±0.22(Predicted)
Appearance
Colorless to light yellow Liquid
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-37/38-41
Safety Statements 
26-39
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5-BROMO-2-ISOPROPOXYPYRIDINE Usage And Synthesis

Uses

5-Bromo-2-isopropylpyridine is used to prepare azepino[4,?5-?b]?indoles as histamine receptor modulators for treating cognitive and psychotic disorders.

Synthesis

75-30-9

13466-38-1

870521-31-6

The general procedure for the synthesis of 5-bromo-2-isopropoxypyridine from 2-iodopropane and 2-hydroxy-5-bromopyridine was as follows: with reference to Example 17, 5-bromo-2-isopropoxypyridine was prepared as follows: 5-bromopyridin-2(1H)-one (5 g, 28.7 mmol) and potassium carbonate (9.93 g, 71.8 mmol) were mixed in dimethyl sulfoxide. 2-Iodopropane (3.73 ml, 37.3 mmol) was slowly added to the reaction mixture at room temperature and stirred continuously at the same temperature for 4 hours. After completion of the reaction, the reaction solution was diluted with ethyl acetate and washed sequentially with water and saturated saline. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to remove the solvent. The resulting crude product was purified by silica gel column chromatography (eluent ratio: ethyl acetate/hexane = 20/80 to 50/50) to afford the target compound 5-bromo-2-isopropoxypyridine (4.72 g, 76% yield) as a colorless oil. Its 1H-NMR (400 MHz, CDCl3) data were as follows: δ1.33 (6H, d, J=6.3 Hz), 5.18-5.28 (1H, m), 6.59 (1H, d, J=8.8 Hz), 7.61 (1H, dd, J=8.8,2.9 Hz), 8.17 (1H, d, J=2.0 Hz).

References

[1] Patent: EP1892241, 2008, A1. Location in patent: Page/Page column 124
[2] ACS Medicinal Chemistry Letters, 2018, vol. 9, # 7, p. 761 - 767
[3] Patent: WO2005/123675, 2005, A1. Location in patent: Page/Page column 54

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