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| | 3-Methyl-1H-pyrazolo[3,4-b]pyridine-5-amine Basic information |
| Product Name: | 3-Methyl-1H-pyrazolo[3,4-b]pyridine-5-amine | | Synonyms: | 3-Methyl-1H-pyrazolo[3,4-b]pyridin-5-aMine;5-AMino-3-Methyl-1H-pyrazolo[3,4-b]pyridine;5-Amino-3-iodo-1H-pyrazolo[3,4-b]pyridine;3-Methyl-1H-pyrazolo[3,4-b]pyridine-5-amine;1H-Pyrazolo[3,4-b]pyridin-5-amine, 3-methyl- | | CAS: | 1186608-73-0 | | MF: | C7H8N4 | | MW: | 148.17 | | EINECS: | | | Product Categories: | | | Mol File: | 1186608-73-0.mol | ![3-Methyl-1H-pyrazolo[3,4-b]pyridine-5-amine Structure](CAS2/GIF/1186608-73-0.gif) |
| | 3-Methyl-1H-pyrazolo[3,4-b]pyridine-5-amine Chemical Properties |
| storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | Appearance | Light yellow to yellow Solid |
| | 3-Methyl-1H-pyrazolo[3,4-b]pyridine-5-amine Usage And Synthesis |
| Synthesis | GENERAL STEPS: 3-methyl-5-nitro-1H-pyrazolo[3,4-b]pyridine (39 mg, 0.22 mmol) and 10% Pd/C (12 mg, 0.011 mmol) were added to a 25 mL round bottom flask. Ethanol (10 mL) was then added and hydrogen was passed into the reaction mixture for 15 min. The reaction flask was stirred under a hydrogen balloon for 4 h. After completion of the reaction, it was filtered through a 0.45 μm PVDF filter. Finally, the solvent was removed to afford 3-methyl-1H-pyrazolo[3,4-b]pyridin-5-amine solid (30 mg, 92% yield). | | References | [1] Patent: WO2009/111279, 2009, A1. Location in patent: Page/Page column 84
[2] Patent: WO2012/135631, 2012, A1. Location in patent: Page/Page column 17
[3] Patent: WO2005/9958, 2005, A1. Location in patent: Page 180-181 |
| | 3-Methyl-1H-pyrazolo[3,4-b]pyridine-5-amine Preparation Products And Raw materials |
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