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1047644-76-7

1047644-76-7 Structure

1047644-76-7 Structure
IdentificationBack Directory
[Name]

1,4-DiMethyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
[CAS]

1047644-76-7
[Synonyms]

1,4-DiMethylpyrazole-5-boronic Acid Pinacol Ester
(1,4-DIMETHYL-1H-PYRAZOL-5-YL)BORONIC ACID PINACOL ESTER
1,4-Dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)
1,4-dimethyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyra...
1,4-dimethyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
1,4-Dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole
1,4-DiMethyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
1H-Pyrazole, 1,4-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
[Molecular Formula]

C11H19BN2O2
[MDL Number]

MFCD12400853
[MOL File]

1047644-76-7.mol
[Molecular Weight]

222.092
Chemical PropertiesBack Directory
[storage temp. ]

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

solid
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C11H19BN2O2/c1-8-7-13-14(6)9(8)12-15-10(2,3)11(4,5)16-12/h7H,1-6H3
[InChIKey]

NOZSCXDKBYFTBH-UHFFFAOYSA-N
[SMILES]

N1(C)C(B2OC(C)(C)C(C)(C)O2)=C(C)C=N1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H315-H335
[Precautionary statements ]

P264-P280-P302+P352-P321-P332+P313-P362-P264-P280-P305+P351+P338-P337+P313P
Spectrum DetailBack Directory
[Spectrum Detail]

1,4-DiMethyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole(1047644-76-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

1,4-DIMETHYLPYRAZOLE

1072-68-0

2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

61676-62-8

1,4-DiMethyl-5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

1047644-76-7

General procedure for the synthesis of 1,4-dimethylpyrazole-5-boronic acid pinacol ester from 1,4-dimethylpyrazole and isopropanol pinacol borate: 1. 1,4-dimethyl-1H-pyrazole (480.0 mg, 4.993 mmol) was dissolved in tetrahydrofuran (20 mL, 300 mmol) at 0 °C and a hexane solution of 1.6 M n-butyllithium (4.7 mL, 7.5 mmol) was slowly added. 2. The reaction solution was stirred at room temperature for 1 hr and then cooled to -78 °C. 3. 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (1.63 mL, 7.99 mmol) was added to the cooled reaction solution. 4. The reaction mixture was stirred at -78 °C for 0.5 h and then slowly warmed to 0 °C (0.5 h). 5. Upon completion of the reaction, the reaction was quenched with saturated saline and extracted with ethyl acetate (3×). 6. The organic phases were combined, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. 7. The residue was purified by fast column chromatography using a gradient elution of ethyl acetate/hexane (0-60%). 8. Purification afforded 142 mg of the target product 1,4-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole as a white solid.

[References]

[1] Patent: WO2008/98104, 2008, A1. Location in patent: Page/Page column 90
[2] Patent: US2013/96144, 2013, A1. Location in patent: Paragraph 0171; 0172
[3] Patent: WO2014/143768, 2014, A1. Location in patent: Page/Page column 109; 110
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