2-Fluoropyridine-5-boronic acid pinacol ester
2-Fluoropyridine-5-boronic acid pinacol ester Basic information
- Product Name:
- 2-Fluoropyridine-5-boronic acid pinacol ester
- Synonyms:
-
- 2-Fluoro-5-pyridineboronic acid pinacol ester
- 2-FLUORO-5-(4 4 5 5-TETRAMETHYL-(1 3 2)&
- 6-FLUOROPYRIDINE-3-BORONIC ACID, PINACOL ESTER
- 2-Fluoro-5-pyridineboronic acid pinacol ester, 2-Fluoro-5-(4,4,5,5-tetramethyl-[1,3,2]-dioxaborolan-2-yl)-pyridine
- 2-Fluoropyridin-5-ylboronic acid pinacol ester
- 2-Fluoropyridine-5-boronic acid pinacol ester
- 2-Fluoropyridine-5-boronic acid pinacol ester >=95%
- 2-Flouropyridine-5-boronic acid pinacol ester
- CAS:
- 444120-95-0
- MF:
- C11H15BFNO2
- MW:
- 223.05
- Mol File:
- 444120-95-0.mol
2-Fluoropyridine-5-boronic acid pinacol ester Chemical Properties
- Melting point:
- 29-33 °C(lit.)
- Boiling point:
- 304.2±27.0 °C(Predicted)
- Density
- 1.09±0.1 g/cm3(Predicted)
- Flash point:
- >230 °F
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- powder to lump
- pka
- -0.44±0.12(Predicted)
- color
- White to Light yellow
- InChI
- InChI=1S/C11H15BFNO2/c1-10(2)11(3,4)16-12(15-10)8-5-6-9(13)14-7-8/h5-7H,1-4H3
- InChIKey
- ZKSRQMCKFLGPQU-UHFFFAOYSA-N
- SMILES
- C1(F)=NC=C(B2OC(C)(C)C(C)(C)O2)C=C1
2-Fluoropyridine-5-boronic acid pinacol ester Usage And Synthesis
Uses
2-Fluoropyridine-5-boronic acid pinacol ester is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Synthesis
766-11-0
73183-34-3
444120-95-0
General procedure for the synthesis of 2-fluoro-5-bromopyridine and pinacol ester of bisboronic acid from 2-fluoro-5-bromopyridine and pinacol ester of bisboronic acid: under nitrogen protection, Pd(dppf)Cl2 (4.16 g, 5.68 mmol) was added in a single step to a solution containing 5-bromo-2-fluoro-pyridine (10 g, 56.82 mmol), pinacol ester of bisboronic acid (21.64 g, 85.23 mmol) and potassium acetate (16.73 g, 170.46 mmol) in a solution of dioxane (100 mL). The mixture was stirred at room temperature for 10 minutes and then heated to reflux for 6 hours. Upon completion of the reaction, the solvent was removed by direct evaporation and the residue was purified by flash silica gel column chromatography to afford the target product 2-fluoropyridine-5-boronic acid pinacol ester (10.5 g, 82.85% yield). The structure of the product was confirmed by 1H NMR (400 MHz, chloroform-d): δ 8.59 (s, 1H), 8.15 (dt, J = 1.76, 8.41 Hz, 1H), 6.91 (dd, J = 2.26, 8.28 Hz, 1H), 1.35 (s, 12H).
References
[1] Patent: EP3333157, 2018, A1. Location in patent: Paragraph 0255; 0256
[2] Patent: EP3239143, 2017, A2. Location in patent: Paragraph 0215
[3] Patent: WO2006/38116, 2006, A2. Location in patent: Page/Page column 40
[4] Patent: EP2891656, 2015, A1. Location in patent: Paragraph 0245
[5] Patent: WO2006/126081, 2006, A2. Location in patent: Page/Page column 52-53
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2-Fluoropyridine-5-boronic acid pinacol ester(444120-95-0)Related Product Information
- N-(2-Fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide
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- 2-FLUORO-3-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PYRIDINE
- 2-Fluoropyridine-5-boronic acid
- 2-FLUORO-5-(4 4 5 5-TETRAMETHYL-(1 3 2)&
- 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
- 2,6-DIFLUORO-3-(4,4,5,5-TETRAMETHYL-[1,3,2]-DIOXABOROLAN-2-YL)PYRIDINE
- 2-FLUORO-4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRIDINE
- 3-CHLORO-2-FLUORO-4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)PYRIDINE
- 5-BROMO-2-FLUORO-3-(4,4,5,5-TETRAMETHYL-[1,3,2]-DIOXABOROLAN-2-YL)PYRIDINE
- 3-FLUORO-4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLA,3-FLUORO-4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)PYRIDINE
- 2,3-DIFLUOROPYRIDINE-5-BORONIC ACID PINACOL ESTER
- 3-TERT-BUTYLOXYCARBONYLAMINO-2-FLUOROPYRIDINE-5-BORONIC ACID PINACOL ESTER
- 5-FLUORO-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-BENZO[B]THIOPHENE
- 6-FLUORO-4-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-1H-INDAZOLE
- 3-(2-FLUORO-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PHENYL)PYRIDINE
- 7-FLUORO-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)INDOLIN-2-ONE
- 4-FLUORO-2-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PYRIDINE