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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19472Generated: October 26, 2026

1-Methylpiperazine → 1-(4-Bromo-2-methylbenzoyl)-4-methylpiperazine

https://huagongshe.com/reaction/19472

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromo-2-methylbenzoic acidHCID 99570—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
SolventDimethylformamideHCID 6228—
Product1-(4-Bromo-2-methylbenzoyl)-4-methylpiperazineHCID 59392754—

Reaction Steps

4-Bromo-2-methylbenzoic acid (10 g, 46.5 mmol), and HBTU (23 g, 60.5 mmol) were dissolved in DMF (150 mL), then N-methyl piperazine (6.0 g, 60.5 mmol) and DIPEA (21 mL, 121 mmol) were added. The reaction was stirred overnight before the removal of the DMF in vacuo, the gum was quenched with 2.0N NaOH (100 mL), extracted with diethyl ether (3×200 mL), dried (MgSO4) and solvent removed in vacuo to yield a viscous gum. Purification on silica using 0-10% MeOH in DCM as eluent, gave the title compound as viscous oil. The oil was dissolved in the minimum amount of diethyl ether, iso-hexane was added to give a colourless solid which was filtered and dried (11.8 g, 86%); 1H NMR (CDCl3) 7.40 (s, 1H), 7.36 (d, 1H), 7.04 (d, 1H), 3.86-3.79 (m, 2H), 3.27-3.21 (m, 2H), 2.51-2.45 (m, 2H), 2.32-2.29 (m, 8H); MH+ 298.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745428B2
Source datasetuspto-grants-2010_06
ORD IDord-737e58edd27a47cbba07fbab19ebb2d9
Source noteuspto-grants-2010_06