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| | 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-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;5-Nitro-1H-pyrrolo[2,3-b]pyridine | | CAS: | 101083-92-5 | | MF: | C7H5N3O2 | | MW: | 163.13 | | EINECS: | | | Product Categories: | Azaindoles | | Mol File: | 101083-92-5.mol | ![5-Nitro-1H-pyrrolo[2,3-b]pyridine Structure](CAS/GIF/101083-92-5.gif) |
| | 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 |
| | 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 | 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]pyridine Preparation Products And Raw materials |
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