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| | 1-Methyl-1H-indazol-5-amine Basic information | | Uses |
| Product Name: | 1-Methyl-1H-indazol-5-amine | | Synonyms: | 1-methyl-5-indazolamine;1-methyl-1H-indazole-5-amine;1H-Indazol-5-amine, 1-methyl-;1-methyl-1H-indazol-5-amine(SALTDATA: FREE);5-AMino-1-Methyl-1H-indaz...;5-aMino-1-Methylindazole;1-METHYL-1H-INDAZOL-5-YLAMINE;1-METHYL-1H-INDAZOL-5-YLAMINE TRIHYDROCHLORIDE | | CAS: | 50593-24-3 | | MF: | C8H9N3 | | MW: | 147.18 | | EINECS: | | | Product Categories: | pharmacetical | | Mol File: | 50593-24-3.mol |  |
| | 1-Methyl-1H-indazol-5-amine Chemical Properties |
| Melting point | 142-144°C | | Boiling point | 321.6±15.0 °C(Predicted) | | density | 1.27±0.1 g/cm3(Predicted) | | storage temp. | Keep in dark place,Inert atmosphere,Room temperature | | form | Crystalline Powder | | pka | 3.85±0.10(Predicted) | | color | Brown |
| Hazard Codes | Xi | | HazardClass | IRRITANT | | HS Code | 29339980 |
| | 1-Methyl-1H-indazol-5-amine Usage And Synthesis |
| Uses | 1-Methyl-5-amino-1H-indazole is used in preparation of Hydrazone compounds having (Hetero)aryl group at terminal Amine group for treating tau protein-associated disease. Also, used in preparation of Dihydroisoindole-1H-pyrazolo[3,4-d]pyrimidinone compounds as Wee1 inhibitors for treatment of kinase-related diseases. | | Uses | 1-Methyl-5-amino-1H-indazole is used in preparation of Hydrazone compounds having (Hetero)aryl group at terminal Amine group for treating tau protein-associated disease. Also, used in preparation of Dihydroisoindole-1H-pyrazolo[3,4-d]pyrimidinone compounds as Wee1 inhibitors for treatment of kinase-related diseases. | | Synthesis | Step 2: Preparation of 1-methyl-1H-indazol-5-amine
Iron powder (5.04 g, 90.3 mmol) was added batchwise to a mixed solution of ethanol (225 mL) and water (100 mL) of 1-methyl-5-nitro-1H-indazole (4.00 g, 22.6 mmol), followed by ammonium chloride (12.1 g, 225 mmol). The reaction mixture was stirred and heated at 80 °C for 1 hour. After completion of the reaction, the reaction mixture was diluted with dichloromethane (500 mL) and filtered to remove insoluble material. The organic layer was separated, dried with anhydrous magnesium sulfate and concentrated under reduced pressure to give the title compound 1-methyl-1H-indazol-5-amine (3.29 g, 99% yield).
HPLC analytical conditions: SYMMETRY C18 column (3.5 μm, 4.6 × 30 mm); mobile phase: acetonitrile/water gradient containing 0.1% trifluoroacetic acid (2%-98% acetonitrile, 10 min); flow rate: 2 mL/min; retention time: 1.06 min.
Mass spectrum (MS): m/z 147.2 ([M+H]+). | | References | [1] Patent: WO2007/88478, 2007, A1. Location in patent: Page/Page column 19
[2] Tetrahedron, 2008, vol. 64, # 28, p. 6711 - 6723
[3] Journal of Chemical Research, Miniprint, 1990, # 11, p. 2601 - 2615
[4] Patent: WO2013/100632, 2013, A1. Location in patent: Page/Page column 95
[5] Patent: US2014/371219, 2014, A1. Location in patent: Paragraph 0662; 0663; 0664 |
| | 1-Methyl-1H-indazol-5-amine Preparation Products And Raw materials |
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