ChemicalBook--->CAS DataBase List--->101083-92-5

101083-92-5

101083-92-5 Structure

101083-92-5 Structure
IdentificationBack Directory
[Name]

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

101083-92-5
[Synonyms]

5-NITRO-7-AZAINDOLE
5-Nitro-7-azaindole,97%
5-Nitro-7-aza-1H-indole
5-NITRO-1H-PYRROLO[2,3-B]PYRIDINE
1H-Pyrrolo[2,3-b]pyridine, 5-nitro-
TIANFU-CHEM 101083-92-5 5-NITRO-1H-PYRROLO[2,3-B]PYRIDINE
[Molecular Formula]

C7H5N3O2
[MDL Number]

MFCD06659682
[MOL File]

101083-92-5.mol
[Molecular Weight]

163.13
Chemical PropertiesBack Directory
[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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[HS Code ]

2933399990
Hazard InformationBack Directory
[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]

1H-Pyrrolo[2,3-b]pyridine, 5-nitro-1-(phenylsulfonyl)-

937012-11-8

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

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
Spectrum DetailBack Directory
[Spectrum Detail]

5-NITRO-1H-PYRROLO[2,3-B]PYRIDINE(101083-92-5)1HNMR
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