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1425045-01-7

1425045-01-7 Structure

1425045-01-7 Structure
IdentificationBack Directory
[Name]

1,3-diMethyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)pyridin-2(1H)-one
[CAS]

1425045-01-7
[Synonyms]

1,5-Dimethyl-6-oxo-1,6-dihydropyridine-3-boronic Acid Pinacol Ester
1,3-dimethyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2-dihydropyridin-2-one
1,3-diMethyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)pyridin-2(1H)-one
1,3-Dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2(1H)-pyridinone
1,3-Dimethyl-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyridin-2-one
2(1H)-Pyridinone, 1,3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
[Molecular Formula]

C13H20BNO3
[MDL Number]

MFCD16996317
[MOL File]

1425045-01-7.mol
[Molecular Weight]

249.11
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

1,3-diMethyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)pyridin-2(1H)-one(1425045-01-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-BroMo-1,3-diMethyl-2-pyridone, 97%

51417-13-1

Bis(pinacolato)diboron

73183-34-3

1,3-diMethyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)pyridin-2(1H)-one

1425045-01-7

The general procedure for the synthesis of 1,3-dimethylpyridin-2(1H)-one-5-pinacol borate from 5-bromo-1,3-dimethylpyridin-2(1H)-one and pinacol bis(boronic acid) ester was carried out as follows: firstly, nitrogen was vented into dioxane for degassing. Subsequently, the degassed dioxane solution (2.0 mL) was added to a mixture containing 5-bromo-1,3-dimethylpyridin-2(1H)-one (75 mg, 0.37 mmol), bis(pinacolato)diboron (113 mg, 0.445 mmol) and KOAc (109 mg, 1.11 mmol). Next, the catalyst PdCl2(dppf)-CH2Cl2 (30 mg, 0.037 mmol) was added. The reaction mixture was heated and reacted at 85 °C for 16 hours. After completion of the reaction, the reaction mixture was diluted with EtOAc and filtered through a Celite pad. Finally, the filtrate was concentrated under vacuum to afford the crude product 1,3-dimethylpyridin-2(1H)-one-5-pinacol borate (169 mg, 0.678 mmol, quantitative yield) as a brown oil.

[References]

[1] Patent: WO2016/196644, 2016, A1. Location in patent: Paragraph 709; 710
[2] Journal of Medicinal Chemistry, 2016, vol. 59, # 10, p. 4462 - 4475
[3] Patent: WO2014/78323, 2014, A1. Location in patent: Paragraph 00584
[4] Patent: US2018/44335, 2018, A1. Location in patent: Paragraph 0459-0460
[5] Patent: WO2018/102452, 2018, A2. Location in patent: Paragraph 693; 694
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