Identification | Back Directory | [Name]
6-CYCLOPROPYL-3-PYRIDINYL BORONIC ACID PINACOL ESTER | [CAS]
893567-09-4 | [Synonyms]
6-Cyclopropylpyridine-3-boronic acid pinacol ester 6-CYCLOPROPYL-3-PYRIDINYL BORONIC ACID PICOL ESTER 2-Cyclopropyl-5-pyridinyl boronic acid pinacol ester 6-CYCLOPROPYL-3-PYRIDINYL BORONIC ACID PINACOL ESTER 2-cyclopropyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine 2-Cyclopropyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) Pyridine, 2-cyclopropyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)- 6-Cyclopropylpyridine-3-boronic acid pinacol ester
6-(Cyclopropyl)pyridine-3-boronic acid pinacol ester | [Molecular Formula]
C14H20BNO2 | [MDL Number]
MFCD09952039 | [MOL File]
893567-09-4.mol | [Molecular Weight]
245.13 |
Chemical Properties | Back Directory | [Boiling point ]
354.1±30.0 °C(Predicted) | [density ]
1.07±0.1 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Store in freezer, under -20°C | [form ]
solid | [pka]
5.90±0.24(Predicted) | [color ]
white to light yellow |
Hazard Information | Back Directory | [Synthesis]
A suspension was prepared in dioxane (10 mL) with 5-bromo-2-cyclopropylpyridine (0.21 g, 1.1 mmol), bis(pinacolato)diboron (0.31 g, 1.2 mmol) and potassium acetate (0.32 g, 3.2 mmol). The suspension was degassed with argon for 10 min and then PdCl2-dppf (0.026 g) was added. The reaction mixture was heated to 80 °C and kept for 15 hours. After completion of the reaction, it was cooled to room temperature and filtered through a diatomaceous earth plug. The filtrate was concentrated to give a black oily substance. The oily substance was dissolved in ether and extracted four times with 1.0 M sodium hydroxide solution. The combined yellow aqueous phases were cooled to 10°C and the pH was adjusted to 6.5 with 2.5 M hydrochloric acid, followed by repeated extraction with ether. The combined organic phases were dried with anhydrous magnesium sulfate, filtered and concentrated to give 0.27 g (103%) of 6-cyclopropylpyridine-3-boronic acid pinacol ester as a yellow oil, which solidified slowly. 1H-NMR analysis showed the product to be about 60-65% pure, with the major impurity being pinacol borane. The crude product can be directly used in the subsequent reaction without further purification.GC-MS m/z 245.2 (M+), 244.2 (M-I); 1H-NMR (CDCl3) δ 8.78 (br s, 1H), 7.93 (dd, 1H), 7.10 (d, 1H), 2.10 (m, 1H), 1.34 (s, 12H), 1.10- 1.00 (m, 4H) ppm. | [References]
[1] Patent: WO2006/65215, 2006, A1. Location in patent: Page/Page column 29 [2] Patent: WO2015/52264, 2015, A1. Location in patent: Paragraph 0556; 0557 [3] Patent: US2018/296543, 2018, A1. Location in patent: Page/Page column 0731; 0732 |
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