ChemicalBook--->CAS DataBase List--->503184-35-8

503184-35-8

503184-35-8 Structure

503184-35-8 Structure
IdentificationBack Directory
[Name]

2-METHOXY-4-METHYL-PYRIDINE-5-BORONIC ACID
[CAS]

503184-35-8
[Synonyms]

2-METHOXY-4-PICOLINE-5-BORONIC ACID
6-Methoxy-4-methylpyridin-3-ylboronicaci
2-Methoxy-4-methylpyridin-5-boronic acid
6-Methoxy-4-methylpyridine-3-boronic acid
6-METHOXY-4-METHYLPYRIDINE-5-BORONIC ACID
6-Methoxy-4-methylpyridin-3-ylboronic acid
2-METHOXY-4-METHYL-PYRIDINE-5-BORONIC ACID
2-METHOXY-4-METHYL-5-PYRIDINYLBORONIC ACID
(6-Methoxy-4-methyl-3-pyridyl)boronic acid
2-Methoxy-4-Methyl-Pyridinyl-5-Boronic Acid
Boronic acid, B-(6-methoxy-4-methyl-3-pyridinyl)-
Boronic acid, (6-methoxy-4-methyl-3-pyridinyl)- (9CI)
2-METHOXY-4-METHYL-PYRIDINE-5-BORONIC ACID ISO 9001:2015 REACH
[Molecular Formula]

C7H10BNO3
[MDL Number]

MFCD07368880
[MOL File]

503184-35-8.mol
[Molecular Weight]

166.97
Chemical PropertiesBack Directory
[Boiling point ]

339.2±52.0 °C(Predicted)
[density ]

1.20±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Store in freezer, under -20°C
[pka]

7.34±0.58(Predicted)
[Appearance]

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

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

37/38-41
[Safety Statements ]

26-39
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

2-METHOXY-4-METHYL-PYRIDINE-5-BORONIC ACID(503184-35-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-Bromo-2-methoxy-4-methylpyridine

164513-39-7

2-METHOXY-4-METHYL-PYRIDINE-5-BORONIC ACID

503184-35-8

Under argon protection, butyl lithium solution (1.6 M in hexane, 15.3 mL, 22.27 mmol) was slowly added dropwise to a solution of 5-bromo-2-methoxy-4-methylpyridine (4.5 g, 22.3 mmol) dissolved in 150 mL of tetrahydrofuran, keeping the reaction temperature at -78 °C. After the reaction mixture was stirred continuously at -78 °C for 1 h, triisopropyl borate (6.2 mL, 26.7 mmol) was added. Subsequently, the reaction system was slowly warmed to room temperature and stirring was continued overnight. Upon completion of the reaction, the mixture was poured into a mixture of equal volumes of saturated aqueous ammonium chloride solution and water and extracted with ethyl acetate. The organic layers were combined, washed with brine, dried over anhydrous sodium sulfate and concentrated. The crude product was washed with ethyl ether to afford 6-methoxy-4-methylpyridine-3-boronic acid as a white solid (2.12 g, 56.6% yield).LRMS (m/z): 168 (M + 1)+.

[References]

[1] Bioorganic and medicinal chemistry letters, 2003, vol. 13, # 2, p. 289 - 291
[2] Patent: EP2738172, 2014, A1. Location in patent: Paragraph 0107
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