Identification | Back Directory | [Name]
2-Amino-3-(trifluoromethyl)pyridine-5-boronic acid pinacol ester | [CAS]
947249-01-6 | [Synonyms]
2-Amino-3-(trifluoromethyl)-pyridine-5-boronic acid picol ester 2-Amino-3-(trifluoromethyl)pyridine-5-boronic acid pinacol ester 6-Amino-5-(trifluoromethyl)pyridine-3-boronic acid pinacol ester (6-AMINO-5-(TRIFLUOROMETHYL)PYRIDIN-3-YL)BORONIC ACID PINACOL ESTER 5-(Tetramethyl-1,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)pyridin-2-amine 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-trifluoromethyl)pyridin-2-amine 3-(trifluoroMethyl)-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-aMine 2-Pyridinamine, 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-(trifluoromethyl)- 3-hydroxy-2,3-dimethylbutan-2-yl hydrogen (6-amino-5-(trifluoromethyl)pyridin-3-yl)boronate | [Molecular Formula]
C12H16BF3N2O2 | [MDL Number]
MFCD12923414 | [MOL File]
947249-01-6.mol | [Molecular Weight]
306.089 |
Chemical Properties | Back Directory | [Melting point ]
132-134℃ | [Boiling point ]
359.1±42.0 °C(Predicted) | [density ]
1.23 | [storage temp. ]
Inert atmosphere,Store in freezer, under -20°C | [pka]
4.31±0.50(Predicted) | [Appearance]
White to off-white Solid |
Hazard Information | Back Directory | [Synthesis]
GENERAL STEPS: 5-bromo-3-(trifluoromethyl)pyridin-2-amine (180 g) was mixed with 1,4-dioxane (3600 mL) in a flask and stirred. Bis(pinacolato)diboron (284.47 g), potassium acetate (109.95 g) and 1,1'-bis(diphenylphosphino)ferrocene palladium(II) dichloride dichloromethane complex (18 g) were added sequentially at 25-30 °C. The reaction mixture was heated to 95-100 °C and maintained for 15-16 hours. After completion of the reaction, it was cooled to 25-30 °C, filtered through a bed of diatomaceous earth and the filter bed was washed with ethyl acetate (1800 mL). The filtrate was concentrated under reduced pressure to give the crude product 2-amino-3-(trifluoromethyl)pyridine-5-boronic acid pinacol ester (450 g).
Purification step: the crude product was dissolved in methanol (1800 mL), activated carbon (45 g) and silica gel (60-120 mesh, 450 g) were added, and stirred at 25-30 °C for 1 hour. The mixture was filtered through a bed of diatomaceous earth and washed with methanol (450 mL). The filtrate was slowly added to cold water (6750 mL) over a period of 1 hour, maintaining the temperature at 0-5 °C. The precipitate was collected by filtration and washed with cold water (900 mL). The wet solid was dried at 45-50 °C to give purified 2-amino-3-(trifluoromethyl)pyridine-5-boronic acid pinacol ester (209 g).
Yield: 97.47%.
Purity: 98.43%.
1H NMR (300 MHz, DMSO-d6): δ 8.38 (s, 1H), 7.80 (s, 1H), 6.92 (s, 2H), 1.27 (s, 12H).
MS: m/z 289.1 (M + 1) | [References]
[1] Patent: WO2015/145369, 2015, A1. Location in patent: Page/Page column 37 [2] Patent: WO2012/34526, 2012, A1. Location in patent: Page/Page column 36-37 [3] Patent: US2013/190307, 2013, A1. Location in patent: Paragraph 0172; 0173 [4] Patent: WO2010/8847, 2010, A2. Location in patent: Page/Page column 147-148 [5] Patent: WO2008/12326, 2008, A1. Location in patent: Page/Page column 69 |
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