Basic information Safety Supplier Related

3-[4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRAZOL-1-YLMETHYL]-PYRIDINE

Basic information Safety Supplier Related

3-[4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRAZOL-1-YLMETHYL]-PYRIDINE Basic information

Product Name:
3-[4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRAZOL-1-YLMETHYL]-PYRIDINE
Synonyms:
  • 3-[4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRAZOL-1-YLMETHYL]-PYRIDINE
  • 3-((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)methyl)pyridine
  • 1-(3-PyridylMethyl)-1H-pyrazole-4-boronic acid pinacol ester
  • 3-{[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]methyl}pyridine
  • 1-(Pyridin-3-ylmethyl)-1H-pyrazole-4-boronic acid, pinacol ester 97%
  • Pyridine, 3-[[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]methyl]-
  • 1-(Pyridin-3-ylmethyl)-1H-pyrazole-4-boronic acid pinacol ester
  • 3-((4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)methyl)pyridine - [T25839]
CAS:
864754-21-2
MF:
C15H20BN3O2
MW:
285.15
Mol File:
864754-21-2.mol
More
Less

3-[4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRAZOL-1-YLMETHYL]-PYRIDINE Chemical Properties

Melting point:
102-106℃
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
solid
Appearance
Off-white to yellow Solid
More
Less

Safety Information

Hazard Codes 
Xn
Risk Statements 
22
HS Code 
2933399990
More
Less

3-[4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRAZOL-1-YLMETHYL]-PYRIDINE Usage And Synthesis

Synthesis

69966-55-8

269410-08-4

864754-21-2

The general procedure for the synthesis of 1-(3-pyridinylmethyl)-1H-pyrazole-4-boronic acid pinacol ester from 3-bromomethylpyridine and 4-pyrazole boronic acid pinacol ester was as follows: 3-bromomethylpyridine (2.67 g, 15.5 mmol) and 4-pyrazole boronic acid pinacol ester (3.01 g, 15.5 mmol) were dissolved in N,N-dimethylformamide (DMF, 20 mL). ) in N,N-dimethylformamide (DMF, 20 mL), followed by addition of potassium carbonate (2.2 g, 16 mmol) to the reaction system. The reaction mixture was heated to 80 °C and the reaction was stirred at this temperature for 8 hours. After completion of the reaction, the mixture was poured into water (50 mL) and extracted with ethyl acetate (50 mL x 3), the organic phases were combined and washed with saturated brine (20 mL) and dried over anhydrous sodium sulfate. After the solvent was removed by concentration under reduced pressure, the residue was purified by column chromatography (eluent: petroleum ether/ethyl acetate, v/v=1/1.5) to give 280 mg of the target product in the form of light yellow oil in 6.33% yield.

References

[1] Patent: CN106749268, 2017, A. Location in patent: Paragraph 0607; 0608

3-[4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRAZOL-1-YLMETHYL]-PYRIDINESupplier

Alfa Aesar
Tel
400-6106006
Email
saleschina@alfa-asia.com
Wuhan Chemwish Technology Co., Ltd
Tel
86-027-67849912
Email
sales@chemwish.com
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.
Tel
025-66113011 17798518460
Email
cfzhang@aikonchem.com
Bide Pharmatech Ltd.
Tel
400-164-7117 13681763483
Email
product02@bidepharm.com