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1002309-48-9

1002309-48-9 Structure

1002309-48-9 Structure
IdentificationBack Directory
[Name]

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

1002309-48-9
[Synonyms]

1-Cyclobutyl-1H-pyrazole-...
1-Cyclodecen-1-yl-boronic acid pinacol ester
1-Cyclobutyl-1H-pyrazole-4-boronic acid pinacol ester
1-Cyclobutyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)
1-cyclobutyl-4-(tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
1-cyclobutyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole
1-Cyclobutyl-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
1H-Pyrazole, 1-cyclobutyl-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-
[Molecular Formula]

C13H21BN2O2
[MDL Number]

MFCD16659010
[MOL File]

1002309-48-9.mol
[Molecular Weight]

248.13
Chemical PropertiesBack Directory
[Boiling point ]

370.2±15.0 °C(Predicted)
[density ]

1.14±0.1 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,Room Temperature
[form ]

solid
[pka]

3.33±0.12(Predicted)
[color ]

Off-white
[InChIKey]

OBCTWWFLJFCNPC-UHFFFAOYSA-N
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H319-H335-H302+H312+H332-H315
[Precautionary statements ]

P280-P301+P312-P305+P351+P338
[HS Code ]

2933199090
Spectrum DetailBack Directory
[Spectrum Detail]

1-Cyclobutyl-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole(1002309-48-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Pyrazoleboronic acid pinacol ester

269410-08-4

Cyclobutyl bromide

4399-47-7

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

1002309-48-9

4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (300 mg, 1.55 mmol) was dissolved in N,N-dimethylformamide (DMF, 5 mL) at 0 °C and under argon protection. Sodium hydride (60% oil solution, 40.8 mg, 1.70 mmol) was added in batches, followed by stirring the reaction mixture for 20 min at room temperature. A DMF (1 mL) solution of bromocyclobutane (209 mg, 1.55 mmol) was added and stirring was continued for 2 hours at room temperature. Upon completion of the reaction, the reaction was quenched with saturated aqueous ammonium chloride solution and then extracted three times with ethyl acetate (EtOAc). The organic phases were combined, washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated. Purification by silica gel column chromatography afforded the target product N-cyclobutyl-pyrazole-4-boronic acid pinacol ester (20A, 40 mg, 5.21% yield). Mass spectrum (ESI): m/z 249.0 ([M+H]+).

[References]

[1] Patent: WO2017/160632, 2017, A1. Location in patent: Page/Page column 96
[2] Patent: WO2018/114786, 2018, A1. Location in patent: Page/Page column 152-153
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