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ChemicalBook >  Product Catalog >  Pharmaceutical intermediates >  Heterocyclic compound >  Pyridine compound >  Dihydropyridine >  5-BROMO-2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE

5-BROMO-2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE

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5-BROMO-2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE Basic information

Product Name:
5-BROMO-2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE
Synonyms:
  • 5-BROMO-2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE
  • 5-BROMO-2,3-DIHYDRO-7-AZAINDOLE
  • BROMO-2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE
  • 3-dihydro-1H-pyrrolo[2
  • 5-broMo-2
  • 5-broMo-1H,2H,3H-pyrrolo[2,3-b]pyridine
  • 5-Bromo-7-azaindoline
  • 1H-Pyrrolo[2,3-b]pyridine, 5-bromo-2,3-dihydro-
CAS:
115170-40-6
MF:
C7H7BrN2
MW:
199.05
EINECS:
634-550-3
Product Categories:
  • CHIRAL CHEMICALS
  • Non-Chiral heterocyclic compounds
  • Heterocycle-Pyridine series
  • Amines and Anilines
  • Heterocycles
Mol File:
115170-40-6.mol
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5-BROMO-2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE Chemical Properties

Melting point:
186-191 (Decomposition)
Boiling point:
315.8±42.0 °C(Predicted)
Density 
1.606
Flash point:
136℃
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
solid
pka
9.31±0.20(Predicted)
color 
Brown
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
24/25
WGK Germany 
3
HS Code 
29339900
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5-BROMO-2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE Usage And Synthesis

Uses

5-Bromo-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine is a useful intermediate for organic synthesis.

Synthesis

10592-27-5

115170-40-6

a) 16.8 g (0.14 mol) of 2,3-dihydro-1H-pyrrolo[2,3-b]pyridine, 24.13 g (0.143 mol) of 48% hydrobromic acid and 260 g of methylene chloride were added to a reaction flask and stirred thoroughly to obtain reaction mixture C; b) The temperature of reaction mixture C was controlled at 25~30°C, and 20.20 g of 20% hydrogen peroxide solution was added slowly dropwise. hydrogen peroxide solution to obtain mixture D; c) Neutralize mixture D using 60 g of saturated aqueous sodium bisulfite solution until the red color of the reaction solution completely disappeared, and carry out partitioning to obtain the organic phase E and the aqueous phase F; d) Wash the organic phase E with 200 g of water; e) Recover the dichloromethane solvent from the organic phase E obtained in step d) to obtain 26.6 g of 5-bromo-2,3-dihydro-1H-pyrrolo[ 2,3-b]pyridine in 95.6% yield and the product was ≥99% pure by liquid chromatography.

References

[1] Patent: CN107987076, 2018, A. Location in patent: Paragraph 0048-0053; 0064-0069; 0074; 0080-0085
[2] Patent: CN105461718, 2016, A. Location in patent: Paragraph 0016
[3] Patent: WO2004/78757, 2004, A2. Location in patent: Page 48; 50-51
[4] Patent: WO2015/157504, 2015, A1. Location in patent: Page/Page column 37
[5] Patent: EP1782811, 2007, A1. Location in patent: Page/Page column 63

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