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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 447464Generated: October 30, 2026

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

https://huagongshe.com/reaction/447464

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 numberUS08481525B2
Source datasetuspto-grants-2013_07
ORD IDord-2eba2c37dc4845a3ad8dc3802f151512
Source noteuspto-grants-2013_07