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| | CAS:1427587-32-3 Basic information |
| Product Name: | CAS:1427587-32-3 | | Synonyms: | CAS:1427587-32-3;(1-METHYL-2-OXO-1,2,3,4-TETRAHYDROQUINOLIN-6-YL)BORONIC ACID PINACOL ESTER;1-methyl-6-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,4-tetrahydroquinolin-2-one;1-Methyl-2-oxo-1,2,3,4-tetrahydroquinoline-6-boronic Acid Pinacol Ester;2(1H)-Quinolinone, 3,4-dihydro-1-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-;1-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroquinolin-2-one;1-Methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroquinolin-2(1H)-one;1-Methyl-1,2,3,4-tetrahydroquinolin-2-one-6-boronic acid pinacol ester | | CAS: | 1427587-32-3 | | MF: | C16H22BNO3 | | MW: | 287.16 | | EINECS: | | | Product Categories: | | | Mol File: | 1427587-32-3.mol |  |
| | CAS:1427587-32-3 Chemical Properties |
| Boiling point | 487.3±45.0 °C(Predicted) | | density | 1.12±0.1 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2-8°C | | pka | 0.65±0.20(Predicted) | | Appearance | White to off-white Solid | | InChI | InChI=1S/C16H22BNO3/c1-15(2)16(3,4)21-17(20-15)12-7-8-13-11(10-12)6-9-14(19)18(13)5/h7-8,10H,6,9H2,1-5H3 | | InChIKey | KBKLZANEYMGZGD-UHFFFAOYSA-N | | SMILES | N1(C)C2=C(C=C(B3OC(C)(C)C(C)(C)O3)C=C2)CCC1=O |
| | CAS:1427587-32-3 Usage And Synthesis |
| Synthesis | To a dry reaction flask was added 6-bromo-1-methyl-3,4-dihydroquinolin-2(1H)-one (3 g, 12.5 mmol), pinacol ester of bisboronic acid (3.81 g, 15.0 mmol), potassium acetate (3.68 g, 37.5 mmol), and dioxane (48 mL). Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane complex (457 mg, 0.625 mmol) was added to the reaction system under argon protection. The reaction mixture was heated to 80 °C and stirred overnight. After completion of the reaction, the reaction mixture was diluted with ethyl acetate, filtered through diatomaceous earth and the filter cake was washed with ethyl acetate (2 x 150 mL). The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography using 0 to 40% ethyl acetate-heptane gradient elution to afford the target product 1-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroquinolin-2(1H)-one (2.63 g, 73% yield) as an off-white solid. Mass spectrum (MS): 288.0 (M+H+). | | References | [1] Patent: US2013/72679, 2013, A1. Location in patent: Paragraph 0545; 0546
[2] Patent: WO2013/37779, 2013, A1. Location in patent: Page/Page column 74; 75
[3] Patent: WO2013/41591, 2013, A1. Location in patent: Page/Page column 65
[4] Patent: WO2014/139981, 2014, A1. Location in patent: Page/Page column 24; 25
[5] Patent: WO2016/66662, 2016, A1. Location in patent: Page/Page column 31 |
| | CAS:1427587-32-3 Preparation Products And Raw materials |
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