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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2281731Generated: November 3, 2026

1-(4-Bromophenyl)-cis-3,5-dimethylpiperazine → 4-(cis-3,5-Dimethylpiperazin-1-yl)phenylboronic acid

https://huagongshe.com/reaction/2281731

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Bromophenyl)-cis-3,5-dimethylpiperazineHCID 66730361—
Reactant(4-(4-Isopropylpiperazin-1-yl)phenyl)boronic acidHCID 66730443—
Product4-(cis-3,5-Dimethylpiperazin-1-yl)phenylboronic acidHCID 58486345—

Reaction Steps

The title compound was synthesized according to the synthesis of 4-(4-isopropylpiperazin-1-yl)phenylboronic acid, except substituting 1-(4-bromophenyl)-cis-3,5-dimethylpiperazine (300 mg, 1.11 mmol). The reaction was quenched with sat. NH4Cl solution, extracted with EtOAc, dried over MgSO4, filtered, and concentrated to dryness. The title compound was isolated by silica gel chromatography (MeOH/CH2Cl2, 6:94 to 1:4) as a yellow solid (59 mg, 23%). 1H NMR (400 MHz, MeOD) δ 7.59 (d, J=6.2 Hz, 2H), 6.91 (d, J=8.2 Hz, 2H), 3.67-3.63 (m, 2H), 3.09-3.01 (m, 2H), 2.32 (t, J=11.6 Hz, 2H), 1.18 (d, J=6.4 Hz, 6H); MS ESI 235.1 [M+H]+, calcd for [C12H19BN2O2+H]+ 235.15.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139563B2
Source datasetuspto-grants-2015_09
ORD IDord-70795a74353c41b6a5d0f0e030a7119c
Source noteuspto-grants-2015_09