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| | 1-N-Boc-3-methyl-indazole-5-boronic acid pinacol ester Basic information | | Application |
| Product Name: | 1-N-Boc-3-methyl-indazole-5-boronic acid pinacol ester | | Synonyms: | 1-N-Boc-3-methyl-indazole-5-boronic acid pinacol ester;3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole-1-carboxylate;3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole-1-carboxylic acid 1,1-dimethylethyl ester;tert-butyl 3-Methyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole-1-carboxylate;(1-(TERT-BUTOXYCARBONYL)-3-METHYL-1H-INDAZOL-5-YL)BORONIC ACID PINACOL ESTER;1-N-Boc-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-3-Methyl-indazole;Tert-butyl 3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indazole-1-carboxylate;1H-Indazole-1-carboxylic acid, 3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-, 1,1-dimethylethyl ester | | CAS: | 864770-82-1 | | MF: | C19H27BN2O4 | | MW: | 358.24 | | EINECS: | | | Product Categories: | | | Mol File: | 864770-82-1.mol |  |
| | 1-N-Boc-3-methyl-indazole-5-boronic acid pinacol ester Chemical Properties |
| Boiling point | 476℃ | | density | 1.12 | | Fp | 242℃ | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | Appearance | White to off-white Solid |
| | 1-N-Boc-3-methyl-indazole-5-boronic acid pinacol ester Usage And Synthesis |
| Application | 1-N-BOC-3-methylindazole-5-boronic acid pinacol ester is an organic synthesis intermediate and pharmaceutical intermediate that can be used in laboratory research and development processes and chemical production processes. | | Synthesis | Potassium acetate (4.73 g, 48.3 mmol) and Pd(dppf)Cl2 (0.66 g, 0.81 mmol) in anhydrous DMF (60 mL) were added to tert-butyl 5-bromo-3-methyl-1H-indazole-1-carboxylate (5.00 g, 16.1 mmol) and pinacol ester of bisboronic acid (4.49 g, 17.7 mmol). The mixture was placed in a vial with a rubber-lined screw cap and degassed by three vacuum/nitrogen cycles. Subsequently, the suspension was heated with stirring at 100 °C for 2 h under nitrogen protection. Upon completion of the reaction, the mixture was cooled to room temperature, mixed with saturated aqueous sodium bicarbonate solution (100 mL) and extracted with ethyl acetate (2 x 150 mL). The organic phases were combined, dried over anhydrous sodium sulfate and concentrated to give the crude product. The crude product was purified by silica gel column chromatography using gradient elution with ethyl acetate/hexane (0% to 15%) to afford the target product tert-butyl 3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole-1-carboxylate as an oil (5.55 g, 96% yield).LCMS (+APCI) m/z. 499 (M+H). | | References | [1] Patent: US2008/153813, 2008, A1. Location in patent: Page/Page column 24 [2] Patent: WO2005/85227, 2005, A1. Location in patent: Page/Page column 37; 76 [3] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 2, p. 673 - 678 [4] Patent: US2008/153813, 2008, A1. Location in patent: Page/Page column 22-23 [5] Patent: US2008/153813, 2008, A1. Location in patent: Page/Page column 23 |
| | 1-N-Boc-3-methyl-indazole-5-boronic acid pinacol ester Preparation Products And Raw materials |
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