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ChemicalBook--->CAS DataBase List--->936694-19-8

936694-19-8

936694-19-8 Structure

936694-19-8 Structure
IdentificationBack Directory
[Name]

tert-Butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)piperazine-1-carboxylate
[CAS]

936694-19-8
[Synonyms]

piperazine-1-carboxylate
t-Butyl 4-[[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl
4-(4-Boc-Piperazinomethyl)phenylboronic acid, pinacol ester
tert-Butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)
4-[(4-Boc-1-piperazinyl)methyl]phenylboronic Acid Pinacol Ester
tert-butyl 4-{[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl}piperazine-1-carboxylate
tert-Butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)piperazine-1-carboxylate
tert-Butyl 4-[[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]piperazine-1-carboxylate
1-Piperazinecarboxylic acid, 4-[[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]-, 1,1-dimethylethyl ester
[Molecular Formula]

C22H35BN2O4
[MDL Number]

MFCD16294502
[MOL File]

936694-19-8.mol
[Molecular Weight]

402.335
Chemical PropertiesBack Directory
[Melting point ]

125-130 °C
[Boiling point ]

486.5±45.0 °C(Predicted)
[density ]

1.10±0.1 g/cm3(Predicted)
[storage temp. ]

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

6.31±0.10(Predicted)
[Appearance]

White to off-white Solid
[CAS DataBase Reference]

936694-19-8
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

tert-Butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)piperazine-1-carboxylate(936694-19-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

TERT-BUTYL 4-(4-BROMOBENZYL)PIPERAZINE-1-CARBOXYLATE

844891-10-7

Bis(pinacolato)diboron

73183-34-3

tert-Butyl 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)piperazine-1-carboxylate

936694-19-8

Step II: Synthesis of tert-butyl 4-[[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methyl]piperazine-1-carboxylate (V-1). Under argon protection, tert-butyl 4-(4-bromobenzyl)piperazine-1-carboxylate (7.5 g, 21.1 mmol), pinacol ester of bis(boronic acid) (8 g, 31.7 mmol) and potassium acetate (4.1 g, 42.2 mmol) were dissolved in DMSO (50 mL). Subsequently [1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloride (0.77 g, 1.06 mmol) was added. The reaction mixture was stirred at 90 °C for 16 hours. The reaction progress was monitored by TLC. Upon completion of the reaction, water (100 mL) was added to the mixture and the product was extracted with ethyl acetate (50 mL x 3). The organic phases were combined, washed sequentially with water (100 mL) and brine (100 mL), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: 2-20% methanol gradient in dichloromethane) to afford the target compound 4-(4-Boc-piperazinylmethyl)phenylboronic acid pinacol ester V-1 (7 g, 82% yield).LCMS: m/z 403.3 ([M+H]+).

[References]

[1] Patent: WO2013/157022, 2013, A1. Location in patent: Page/Page column 54-55
[2] Patent: US2015/64196, 2015, A1. Location in patent: Paragraph 0177
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