Basic information Safety Supplier Related

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

Basic information Safety Supplier Related

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

Product Name:
5-NITRO-1H-PYRROLO[2,3-B]PYRIDINE
Synonyms:
  • 1H-Pyrrolo[2,3-b]pyridine, 5-nitro-
  • 5-Nitro-7-aza-1H-indole
  • 5-NITRO-1H-PYRROLO[2,3-B]PYRIDINE
  • 5-NITRO-7-AZAINDOLE
  • 5-Nitro-7-azaindole,97%
  • TIANFU-CHEM 101083-92-5 5-NITRO-1H-PYRROLO[2,3-B]PYRIDINE
  • 5-nitro-1H-pyrrolo[2,3-b]pyridine 97%min
CAS:
101083-92-5
MF:
C7H5N3O2
MW:
163.13
Product Categories:
  • Azaindoles
Mol File:
101083-92-5.mol
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5-NITRO-1H-PYRROLO[2,3-B]PYRIDINE Chemical Properties

Melting point:
280℃
Boiling point:
392.8±35.0 °C(Predicted)
Density 
1.58±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
form 
solid
pka
0.65±0.20(Predicted)
color 
yellow
InChI
InChI=1S/C7H5N3O2/c11-10(12)6-3-5-1-2-8-7(5)9-4-6/h1-4H,(H,8,9)
InChIKey
INMIPMLIYKQQID-UHFFFAOYSA-N
SMILES
C12NC=CC1=CC([N+]([O-])=O)=CN=2
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Safety Information

HS Code 
2933399990
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5-NITRO-1H-PYRROLO[2,3-B]PYRIDINE Usage And Synthesis

Uses

5-Nitro-1H-pyrrolo[2,3-b]pyridine is a reagent used in the synthesis of Cdc7 kinase inhibitors used as a novel cancer therapy. Also an intermediate in the synthesis of 4-anilinoquinazolines as potential anticancer agents.

Synthesis

937012-11-8

101083-92-5

To a stirred suspension of 5-nitro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine (10.2 g, 33 mmol) in methanol (250 mL) was added powdered sodium hydroxide (2 g, 50 mmol) in batches. After stirring the reaction mixture for 30 min at room temperature, powdered sodium hydroxide (2 g, 50 mmol) and dichloromethane (50 mL) were added again and stirring was continued for 30 min. Upon completion of the reaction, the mixture was concentrated, followed by the addition of a mixed solution of 2N HCl (50 mL) and water (200 mL), and the resulting mixture was filtered. The yellow filter cake was washed with water and dried to afford 5-nitro-1H-pyrrolo[2,3-b]pyridine (4.6 g, 28.2 mmol, 85% yield). The product was characterized by 1H-NMR (DMSO-d6) with the following chemical shift δ (ppm): 6.78 (dd, J = 3.50, 1.83 Hz, 1H), 7.79 (dd, J = 3.35, 2.59 Hz, 1H), 8.90-8.92 (m, 1H), 9.13 (d, J = 2.59 Hz, 1H), 12.05- 12.92 (m, 1H).

References

[1] Patent: US2007/112020, 2007, A1. Location in patent: Page/Page column 36

5-NITRO-1H-PYRROLO[2,3-B]PYRIDINESupplier

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