Basic information Safety Supplier Related

5-Bromo-3-chloro-1H-pyrrolo[2,3-b]pyridine

Basic information Safety Supplier Related

5-Bromo-3-chloro-1H-pyrrolo[2,3-b]pyridine Basic information

Product Name:
5-Bromo-3-chloro-1H-pyrrolo[2,3-b]pyridine
Synonyms:
  • 5-Bromo-3-chloro-1H-pyrrolo[2,3-b]pyridine
  • 5-Bromo-3-chloro-7-azaindole
  • 5-Bromo-3-chloro-7-azaindole 96%
  • 1H-Pyrrolo[2,3-b]pyridine, 5-bromo-3-chloro-
  • 3-chloro-5-Bromo-7-azaindole
CAS:
951626-91-8
MF:
C7H4BrClN2
MW:
231.48
Product Categories:
  • Heterocycle-Pyridine series
Mol File:
951626-91-8.mol
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5-Bromo-3-chloro-1H-pyrrolo[2,3-b]pyridine Chemical Properties

Melting point:
216-220 °C
Density 
1.878±0.06 g/cm3(Predicted)
storage temp. 
2-8°C
pka
11.33±0.40(Predicted)
form 
powder
Appearance
Off-white to pink Solid
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-37/38-41
Safety Statements 
26-36/37/39-45
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
HS Code 
2933998090
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5-Bromo-3-chloro-1H-pyrrolo[2,3-b]pyridine Usage And Synthesis

Synthesis

183208-35-7

951626-91-8

The general procedure for the synthesis of 5-bromo-3-chloro-1H-pyrrolo[2,3-b]pyridine from 5-bromo-7-azaindole was as follows: 0.50 g (2.54 mmol) of 5-bromo-1H-pyrrolo[2,3-b]pyridine was dissolved in 10 mL of N,N-dimethylformamide, followed by the addition of 0.37 g (2.79 mmol) of N-chloro-butanedi imide and 0.38 g (2.79 mmol) of dibenzoyl peroxide. The reaction mixture was stirred at room temperature for 18 hours. Upon completion of the reaction, it was extracted with ethyl acetate and distilled water and the organic layer was concentrated under reduced pressure. The residue was purified by column chromatography to afford 0.50 g (85.0% yield) of the target compound 5-bromo-3-chloro-1H-pyrrolo[2,3-b]pyridine.1H NMR (DMSO-d6) δ: 12.24 (br s, 1H), 8.35 (s, 1H), 8.14 (s, 1H), 8.03 (d, 1H), 7.81 (m, 1H ), 7.77 (s, 1H), 7.64 (t, 1H).

References

[1] Journal of Organic Chemistry, 2018, vol. 83, # 2, p. 930 - 938
[2] Patent: WO2016/129933, 2016, A2. Location in patent: Page/Page column 48

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