ChemicalBook--->CAS DataBase List--->229009-40-9

229009-40-9

229009-40-9 Structure

229009-40-9 Structure
IdentificationBack Directory
[Name]

4-(4-Methylpiperazin-1-yl)phenylboronic Acid
[CAS]

229009-40-9
[Synonyms]

4-(4-Methylpiperazino)benzeneboronic acid
4-(4-Methyl-1-piperazinyl)phenylboronic Acid
4-(4-Methylpiperazin-1-yl)phenylboronic Acid
4-(4-Methylpiperazin-1-yl)phenylboronic acid 96%
Boronic acid, B-[4-(4-methyl-1-piperazinyl)phenyl]-
[Molecular Formula]

C11H17BN2O2
[MDL Number]

MFCD11223486
[MOL File]

229009-40-9.mol
[Molecular Weight]

220.08
Chemical PropertiesBack Directory
[Boiling point ]

406.2±55.0 °C(Predicted)
[density ]

1.20±0.1 g/cm3(Predicted)
[storage temp. ]

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

solid
[pka]

9.08±0.17(Predicted)
[color ]

White
[InChI]

InChI=1S/C11H17BN2O2/c1-13-6-8-14(9-7-13)11-4-2-10(3-5-11)12(15)16/h2-5,15-16H,6-9H2,1H3
[InChIKey]

LSKYURVDOIDSCG-UHFFFAOYSA-N
[SMILES]

B(C1=CC=C(N2CCN(C)CC2)C=C1)(O)O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

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

P260-P280-P301+P312
[HS Code ]

2933998090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

1-(4-Bromo-phenyl)-4-methyl-piperazine-->Tetrahydrofuran
Hazard InformationBack Directory
[Uses]

[4-(4-Methylpiperazin-1-yl)phenyl]boronic Acid is a useful synthetic compound.
[Synthesis]

Triisopropyl borate

5419-55-6

1-(4-BROMO-PHENYL)-4-METHYL-PIPERAZINE

130307-08-3

4-(4-Methylpiperazin-1-yl)phenylboronic Acid

229009-40-9

(ii) Preparation of 53c: 4-(4-methylpiperazin-1-yl)phenylboronic acid To a solution of 53b (390 mg, 1.52 mmol) and THF (10 mL), n-butyllithium (0.79 mL, 2.5 M hexane solution) was slowly added at -78 °C and stirred for 10 min. Subsequently, triisopropyl borate (1.75 mL, 7.64 mmol) was added at the same temperature. The reaction mixture was slowly warmed to room temperature and then the reaction was quenched with phosphoric acid. The reaction mixture was neutralized with saturated NaHCO3 solution and subsequently extracted with EtOAc (3 x 10 mL). The organic phases were combined, dried with anhydrous Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, 0-10% MeOH in CH2Cl2 solution) to afford the target product 4-(4-methyl-1-piperazinyl)phenylboronic acid (180 mg, 58%). 1H NMR (300 MHz, CD3OD) δ 2.32 (s, 3H), 2.55 (m, 4H), 3.03 (s, 1H), 3.21 (m, 3H), 6.69-7.59 (m, 4H).

[References]

[1] Patent: US8324264, 2012, B1. Location in patent: Page/Page column 181
[2] Patent: EP2712863, 2014, A1. Location in patent: Paragraph 0435; 0436
Spectrum DetailBack Directory
[Spectrum Detail]

4-(4-Methylpiperazin-1-yl)phenylboronic Acid(229009-40-9)1HNMR
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