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1H-Pyrrolo[2,3-c]pyridine,7-methoxy-(9CI)

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1H-Pyrrolo[2,3-c]pyridine,7-methoxy-(9CI) Basic information

Product Name:
1H-Pyrrolo[2,3-c]pyridine,7-methoxy-(9CI)
Synonyms:
  • 1H-Pyrrolo[2,3-c]pyridine,7-methoxy-(9CI)
  • 7-methoxy pyrrolo[2,3-c]pyridine
  • 7-Metho×y-1H-pyrrolo[2,3-c]pyridine
  • 1H-Pyrrolo[2,3-c]pyridine, 7-methoxy-
  • 7-Methoxy-6-azaindole
  • 7-Methoxy-6-azaindole 98%
CAS:
160590-40-9
MF:
C8H8N2O
MW:
148.16
Product Categories:
  • Heterocycles series
  • PYRIDINE
  • API intermediates
  • Fused Ring Systems
Mol File:
160590-40-9.mol
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1H-Pyrrolo[2,3-c]pyridine,7-methoxy-(9CI) Chemical Properties

Melting point:
110-114℃
Boiling point:
304℃
Density 
1.244
Flash point:
105℃
storage temp. 
Sealed in dry,Room Temperature
form 
powder
pka
14.15±0.40(Predicted)
color 
Yellow
InChI
InChI=1S/C8H8N2O/c1-11-8-7-6(2-4-9-7)3-5-10-8/h2-5,9H,1H3
InChIKey
RHEGHTSBMVYYAM-UHFFFAOYSA-N
SMILES
C1(OC)=NC=CC2C=CNC1=2
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-37/38-41
Safety Statements 
26-39
WGK Germany 
3
HS Code 
2933998090
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1H-Pyrrolo[2,3-c]pyridine,7-methoxy-(9CI) Usage And Synthesis

Synthesis

364046-14-0

160590-40-9

Step 2: (0648) To a solution of 2-(2-methoxy-3-nitropyridin-4-yl)-N,N-dimethylethylamine (5.9 g, 26 mmol) prepared in Step 1 in ethanol (275 mL) was added 10% palladium carbon (Degussa type, 1.5 g). The reaction mixture was placed under hydrogen atmosphere (15 psi) and shaken for 15 min. Upon completion of the reaction, the reaction mixture was filtered through a bed of diatomaceous earth and washed with dichloromethane (DCM). The filtrate was concentrated under reduced pressure to afford 7-methoxy-1H-pyrrolo[2,3-c]pyridine (4.3 g, 61% yield).

References

[1] Journal of Organic Chemistry, 2001, vol. 66, # 17, p. 5723 - 5730
[2] Journal of Organic Chemistry, 2001, vol. 66, # 17, p. 5723 - 5730
[3] Patent: US2015/307465, 2015, A1. Location in patent: Paragraph 0648

1H-Pyrrolo[2,3-c]pyridine,7-methoxy-(9CI)Supplier

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