4-(4-Methylpiperazin-1-yl)phenylboronic Acid
4-(4-Methylpiperazin-1-yl)phenylboronic Acid Basic information
- Product Name:
- 4-(4-Methylpiperazin-1-yl)phenylboronic Acid
- Synonyms:
-
- 4-(4-Methyl-1-piperazinyl)phenylboronic Acid
- 4-(4-Methylpiperazin-1-yl)phenylboronic Acid
- Boronic acid, B-[4-(4-methyl-1-piperazinyl)phenyl]-
- 4-(4-Methylpiperazin-1-yl)phenylboronic acid 96%
- 4-(4-Methylpiperazino)benzeneboronic acid
- 4-(4-Methyl-1-piperazinyl)phenylboronic Acid(contains varying amounts of Anhydride)
- 4-(N-Methylpiperazin-1-yl)phenylboronic acid
- [4-(4-methylpiperazin-1-yl)phenyl]boronic acid - [M22502]
- CAS:
- 229009-40-9
- MF:
- C11H17BN2O2
- MW:
- 220.08
- Product Categories:
-
- Boronate Ester
- Boronic Acid
- Potassium Trifluoroborate
- Mol File:
- 229009-40-9.mol
4-(4-Methylpiperazin-1-yl)phenylboronic Acid Chemical Properties
- 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
- pka
- 9.08±0.17(Predicted)
- form
- solid
- 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
4-(4-Methylpiperazin-1-yl)phenylboronic Acid Usage And Synthesis
Uses
[4-(4-Methylpiperazin-1-yl)phenyl]boronic Acid is a useful synthetic compound.
Synthesis
5419-55-6
130307-08-3
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
4-(4-Methylpiperazin-1-yl)phenylboronic Acid Preparation Products And Raw materials
Raw materials
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