ChemicalBook--->CAS DataBase List--->947249-01-6

947249-01-6

947249-01-6 Structure

947249-01-6 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

2-Amino-3-(trifluoromethyl)pyridine-5-boronic acid pinacol ester(947249-01-6)1HNMR
2-Amino-3-(trifluoromethyl)pyridine-5-boronic acid pinacol ester(947249-01-6)19FNMR
Hazard InformationBack Directory
[Synthesis]

2-Amino-5-bromo-3-(trifluoromethyl)pyridine

79456-34-1

Bis(pinacolato)diboron

73183-34-3

2-Amino-3-(trifluoromethyl)pyridine-5-boronic acid pinacol ester

947249-01-6

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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