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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466280Generated: November 1, 2026

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

https://huagongshe.com/reaction/1466280

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 numberUS08999968B2
Source datasetuspto-grants-2015_04
ORD IDord-df968fdb18724e7b944a60e51c65f975
Source noteuspto-grants-2015_04