| Identification | Back Directory | [Name]
1-(2-(pyrrolidin-1-yl)ethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole | [CAS]
1000802-52-7 | [Synonyms]
1-(2-(Pyrrolidin-1-yl) 1-(2-(pyrrolidin-1-yl)ethyl)-4-(4,4,5,5-tetramethyl-1,3,2-di... 1-[2-(pyrrolidin-1-yl)ethyl]-4-(tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole 1-[2-(1-Pyrrolidinyl)ethyl]-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole 1-(2-(pyrrolidin-1-yl)ethyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole 1H-Pyrazole, 1-[2-(1-pyrrolidinyl)ethyl]-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)- | [Molecular Formula]
C15H26BN3O2 | [MDL Number]
MFCD16659795 | [MOL File]
1000802-52-7.mol | [Molecular Weight]
291.2 |
| Chemical Properties | Back Directory | [Boiling point ]
416.9±25.0 °C(Predicted) | [density ]
1.11±0.1 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Store in freezer, under -20°C | [pka]
9.83±0.20(Predicted) | [Appearance]
White to off-white Solid |
| Hazard Information | Back Directory | [Synthesis]
The reaction was carried out with 4-pyrazoleboronic acid pinacol ester (1.7 g, 8.8 mmol) and N-(2-chloroethyl)pyrrolidine hydrochloride (1.48 g, 8.70 mmol) in the presence of potassium carbonate (3.7 g, 27.00 mmol) for 6 hours at 80 °C with stirring in DMF (15 mL). After completion of the reaction, the reaction mixture was diluted with water (50 mL) and extracted with dichloromethane (50 mL x 3). The organic layers were combined, washed with saturated aqueous sodium chloride solution (15 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography with dichloromethane/ethyl acetate (v/v, 20/1) as eluent to afford the light yellow liquid product 1-[2-(1-pyrrolidinyl)ethyl]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (1.27 g, 50.10% yield). Mass spectrum (ESI, positive ion mode) m/z: 292.10 [M + 1]+. | [References]
[1] Patent: WO2016/615, 2016, A1. Location in patent: Paragraph 00719 [2] Patent: US2010/273796, 2010, A1. Location in patent: Page/Page column 20-21 [3] Patent: US2011/34474, 2011, A1. Location in patent: Page/Page column 22 [4] Patent: US2011/71153, 2011, A1. Location in patent: Page/Page column 21 [5] Patent: US2011/92498, 2011, A1. Location in patent: Page/Page column 20-21 |
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Cool Pharm, Ltd
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