ChemicalBook--->CAS DataBase List--->944401-67-6

944401-67-6

944401-67-6 Structure

944401-67-6 Structure
IdentificationBack Directory
[Name]

2-Amino-6-fluoro pyridine-5-boronic acid pinacol ester
[CAS]

944401-67-6
[Synonyms]

2-Amino-6-fluoro pyridine-5-boronic acid picol ester
6-Amino-2-fluoropyridine-3-boronic acid pinacol ester
2-Fluoro-6-aminopyridine-3-boronic acid pinacol ester
2-Amino-6-fluoro pyridine-5-boronic acid pinacol ester
6-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-amine
2-Pyridinamine, 6-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
6-fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2-dihydropyridin-2-imine
[Molecular Formula]

C11H16BFN2O2
[MDL Number]

MFCD12923416
[MOL File]

944401-67-6.mol
[Molecular Weight]

238.07
Chemical PropertiesBack Directory
[density ]

1.15
[storage temp. ]

2-8°C(protect from light)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Spectrum DetailBack Directory
[Spectrum Detail]

2-Amino-6-fluoro pyridine-5-boronic acid pinacol ester(944401-67-6)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-bromo-6-fluoropyridin-2-amine

944401-65-4

Bis(pinacolato)diboron

73183-34-3

2-Amino-6-fluoro pyridine-5-boronic
 acid pinacol ester

944401-67-6

To a dry 50 mL three-necked flask was added 2-amino-5-bromo-6-fluoropyridine (370 mg, 1.93 mmol), potassium acetate (569 mg, 5.8 mmol), pinacol ester of bis(boronic acid) (538 mg, 2.12 mmol) and dioxane (15 mL). After bubbling through argon for 15 minutes, 1,1'-bis(diphenylphosphino)ferrocene palladium(II) chloride dichloromethane adduct (79 mg, 0.09 mmol) was added. The reaction mixture was refluxed in an oil bath at 115 °C for 4 h under argon protection. After completion of the reaction, the solvent was removed by distillation under reduced pressure and ethyl acetate (150 mL) was added to dissolve the residue. The organic phase was washed sequentially with water (3 x 40 mL) and saturated sodium chloride solution (300 mL), dried over anhydrous sodium sulfate, filtered and concentrated. Purification by silica gel column chromatography (eluent: 30% ethyl acetate/hexane) afforded the target product 2-fluoro-6-amino-5-pyridineboronic acid ester (161 mg, 35% yield).LC-MS (m/z): 157 ([M+H]+ of boronic acid from in situ hydrolysis product in liquid chromatography).1H NMR (CDCl3): δ 7.86 (t, J = 8.4 Hz, 1H), 6.29 (dd, J = 8.1, 2.7 Hz, 1H), 4.70 (br s, 2H), 1.32 (s, 12H).

[References]

[1] Patent: WO2007/84786, 2007, A1. Location in patent: Page/Page column 101-102
[2] Patent: WO2012/109423, 2012, A1. Location in patent: Page/Page column 24
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