Basic information Safety Supplier Related

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

Basic information Safety Supplier Related

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

Product Name:
2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE
Synonyms:
  • 2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE
  • 2,3-Dihydro-7-azaindole 98%
  • 7-azaindoline
  • 1H-Pyrrolo[2,3-b]pyridine,2,3-dihydro-(6CI,8CI,9CI)
  • 2,3-Dihydro-1H-pyrrolo[2,3-b]pyridine 7-azaindoline
  • 2,3-Dihydro-7-azaindole
  • 1H,2H,3H-pyrrolo[2,3-b]pyridine
  • 2,3-Dihydropyrrolo[2,3-b]pyridine, 97+%
CAS:
10592-27-5
MF:
C7H8N2
MW:
120.15
Product Categories:
  • PYRROLIDINE
  • API intermediates
Mol File:
10592-27-5.mol
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2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE Chemical Properties

Melting point:
78-83 °C
Boiling point:
114°C/10mmHg(lit.)
Density 
1.23
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
soluble in Methanol
pka
10.75±0.20(Predicted)
form 
Powder
color 
White
Water Solubility 
Slightly soluble in water.
λmax
306nm(Cyclohexane)(lit.)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36
Safety Statements 
36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29339900
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2,3-DIHYDRO-1H-PYRROLO[2,3-B]PYRIDINE Usage And Synthesis

Chemical Properties

Beige powder

Uses

It can be used as pharmaceutical raw material and intermediate.

Synthesis

271-63-6

10592-27-5

a) 7-azaindole (100 g, 0.846 mol), Ni/Al?O? catalyst (12 g, 10 wt%), and toluene (200 g) were added to the autoclave and stirred and mixed homogeneously to obtain the reaction solution A; b) the autoclave was replaced with nitrogen for 8 times, followed by hydrogen for 4 times to ensure that the reaction system was oxygen-free; c) the reaction solution A was subjected to hydrogenation reaction at a pressure of 2 MPa hydrogen and 130 °C; d) after the completion of the reaction, the hydrogenation mixture was filtered to remove the catalyst to obtain the filtrate B; e) after distillation and recovery of the organic solvent from the filtrate B, 2,3-dihydro-1H-pyrrolo[2,3-b]pyridine (94.59 g, 93.4% yield) was obtained, and the purity of the product was analyzed by gas chromatography, which was ≥98%.

References

[1] Patent: CN107987076, 2018, A. Location in patent: Paragraph 0043-0047; 0058-0063; 0075-0079
[2] Patent: CN106188050, 2016, A. Location in patent: Paragraph 0016
[3] Patent: US2011/144105, 2011, A1. Location in patent: Page/Page column 16
[4] Synthesis, 2005, # 15, p. 2503 - 2506
[5] Patent: WO2004/78757, 2004, A2. Location in patent: Page 32; 48-49

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