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1231930-37-2

1231930-37-2 Structure

1231930-37-2 Structure
IdentificationBack Directory
[Name]

1H-BenziMidazole, 4-fluoro-2-Methyl-1-(1-Methylethyl)-6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-
[CAS]

1231930-37-2
[Synonyms]

Abemaciclib Impurity 2
intermediate-1(Abemaciclib)
(4-FLUORO-1-ISOPROPYL-2-METHYL-1H-BENZO[D]IMIDAZOL-6-YL)BORONIC ACID PINACOL ESTER
4-fluoro-2-methyl-1-propan-2-yl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzimidazole
4-fluoro-2-methyl-1-(propan-2-yl)-6-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-1,3-benzodiazole
4-FLUORO-1-ISOPROPYL-2-METHYL-6-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-1H-BENZOIMIDAZOLE
4-fluoro-1-isopropyl-2-Methyl-6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-benzo[d]iMidazole
4-fluoro-1-isopropyl-2-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolane-2-yl)-1H-benzo[d]imidazole
1H-BENZIMIDAZOLE, 4-FLUORO-2-METHYL-1-(1-METHYLETHYL)-6-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN- 2-Y
4-Fluoro-2-methyl-1-(1-methylethyl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-benzimidazole
1H-BenziMidazole, 4-fluoro-2-Methyl-1-(1-Methylethyl)-6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-
1H-BenziMidazole, 4-fluoro-2-Methyl-1-(1-Methylethyl)-6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)- ISO 9001:2015 REACH
1H-BenziMidazole, 4-fluoro-2-Methyl-1-(1-Methylethyl)-6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)- 4-fluoro-1-isopropyl-2-Methyl-6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-benzo[d]iMidazole intermediate-1(Abemaciclib)
[EINECS(EC#)]

1592732-453-0
[Molecular Formula]

C17H24BFN2O2
[MDL Number]

MFCD25977327
[MOL File]

1231930-37-2.mol
[Molecular Weight]

318.19
Chemical PropertiesBack Directory
[Boiling point ]

442.7±30.0 °C(Predicted)
[density ]

1.12±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

4.32±0.10(Predicted)
[Appearance]

Off-white to yellow Solid
[InChI]

InChI=1S/C17H24BFN2O2/c1-10(2)21-11(3)20-15-13(19)8-12(9-14(15)21)18-22-16(4,5)17(6,7)23-18/h8-10H,1-7H3
[InChIKey]

HUSPISQCNSLJSR-UHFFFAOYSA-N
[SMILES]

C1(C)N(C(C)C)C2=CC(B3OC(C)(C)C(C)(C)O3)=CC(F)=C2N=1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

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

1H-BenziMidazole, 4-fluoro-2-Methyl-1-(1-Methylethyl)-6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-(1231930-37-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

6-Bromo-4-fluoro-1-isopropyl-2-methyl-1H-benzo[d]imidazole

1231930-33-8

Bis(pinacolato)diboron

73183-34-3

1H-BenziMidazole, 4-fluoro-2-Methyl-1-(1-Methylethyl)-6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-

1231930-37-2

The general procedure for the synthesis of 4-fluoro-1-isopropyl-2-methyl-6-boronic acid pinacol ester-based-1H-benzo[d]imidazole from 6-bromo-4-fluoro-1-isopropyl-2-methyl-1H-benzo[d]imidazole and bis(pinacolato)diboron was carried out as follows: in a 500 mL single-necked flask, DMSO (100 mL), followed by sequential addition of 6-bromo-4-fluoro-1- isopropyl-2-methyl-1H-benzo[D]imidazole (20.0 g, 73.80 mmol), bis(pinacolato)diboron (27.6 g, 108.69 mmol), tricyclohexylphosphine (3.53 g, 12.61 mmol) and potassium acetate (21.3 g, 217.38 mmol) were added sequentially. After rapid addition of palladium acetate (1.5 g), the reaction flask was protected by passing nitrogen into the flask and subsequently heated to 90 °C under nitrogen atmosphere. After 3 hours of reaction, the reaction flask was cooled to room temperature and the reaction mixture was poured into 700 mL of water, stirred thoroughly and filtered under reduced pressure. The filter cake was washed twice with 100 mL of water and dried to give a light brown solid. The crude product was pulped with 50 mL of petroleum ether and 10 mL of ethyl acetate for 10 min, and was vacuum filtered to give a white solid (18.8 g, 80.3% yield).

[References]

[1] Patent: CN107266421, 2017, A. Location in patent: Paragraph 0042; 0043; 0050; 0051
[2] Patent: CN104910137, 2017, B. Location in patent: Paragraph 0213; 0220-0222
[3] Patent: EP3091008, 2016, A1. Location in patent: Paragraph 0177; 0178
[4] Patent: US2010/160340, 2010, A1. Location in patent: Page/Page column 10
[5] Patent: WO2015/130540, 2015, A1. Location in patent: Page/Page column 22
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