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1000801-76-2

1000801-76-2 Structure

1000801-76-2 Structure
IdentificationBack Directory
[Name]

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

1000801-76-2
[Synonyms]

(1-(3-METHOXYPROPYL)-1H-PYRAZOL-4-YL)BORONIC ACID PINACOL ESTER
1-(3-Methoxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborola...
1-(3-methoxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole
1-(3-Methoxypropyl)-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
1H-Pyrazole, 1-(3-Methoxypropyl)-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-
[Molecular Formula]

C13H23BN2O3
[MDL Number]

MFCD16659789
[MOL File]

1000801-76-2.mol
[Molecular Weight]

266.14
Chemical PropertiesBack Directory
[Boiling point ]

375.2±22.0 °C(Predicted)
[density ]

1.05±0.1 g/cm3(Predicted)
[storage temp. ]

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

2.00±0.10(Predicted)
[Appearance]

Colorless to light yellow Liquid
Safety DataBack Directory
[HS Code ]

2933199090
Spectrum DetailBack Directory
[Spectrum Detail]

1-(3-Methoxypropyl)-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole(1000801-76-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-(3-methoxypropyl)-1H-pyrazol-4-amine

1183903-41-4

Bis(pinacolato)diboron

73183-34-3

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

1000801-76-2

Potassium acetate (2.4 g, 24 mmol) and Pd(dppf)Cl2 (900 mg, 1.22 mmol) were sequentially added in DMSO (20 mL) as 4-bromo-1-(3-methoxypropyl)-1H-pyrazole (2.1 g, 9.6 mmol) and pinacol ester of bisboronic acid (3.7 g, 15 mmol). The reaction mixture was stirred at 100 °C for 13 h under nitrogen protection. After completion of the reaction, it was cooled to room temperature and the reaction was quenched with saturated aqueous NaCl solution (30 mL). The mixture was extracted with dichloromethane (30 mL x 3), the organic layers were combined and dried with anhydrous Na2SO4. After concentration under reduced pressure, the residue was purified by silica gel column chromatography with the eluent of petroleum ether/ethyl acetate (2:1, v/v) to afford the light yellow oily target product 1-(3-methoxypropyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (1.3 g, 51% yield). Mass spectrum (ESI, positive ion mode) m/z: 267.0 [M + 1]+.

[References]

[1] Patent: WO2016/615, 2016, A1. Location in patent: Paragraph 00598
[2] Patent: WO2010/129848, 2010, A2. Location in patent: Page/Page column 24-25
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