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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267519Generated: November 2, 2026

1-Methylpiperazine → 2-Chloro-N-methyl-4-(4-methyl-piperazin-1-yl)-benzamide

https://huagongshe.com/reaction/1267519

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant2-chloro-4-fluoro-N-methylbenzamideHCID 17144535—
Product2-Chloro-N-methyl-4-(4-methyl-piperazin-1-yl)-benzamideHCID 1854650352.5%

Reaction Steps

A mixture of 316 mg (1.68 mmol) 2-chloro-4-fluoro-N-methyl-benzamide and 0.94 ml (8.4 mmol) 1-methylpiperazine was heated at 140° for 7 h in a sealed glass tube. After cooling to room temperature excess 1-methylpiperazine was removed by distillation at 50°/0.5 mbar. The residue was partitioned between 25 ml CH2Cl2/2 N NaOH solution. The layers were separated and the aqueous layer was extracted with 3 15-ml portions of dichloromethane. The combined organic extracts were dried (Na2SO4) and evaporated. Chromatography (SiO2, CH2Cl2/methanol 19:1) yielded 236 mg (52%) 2-Chloro-N-methyl-4-(4-methyl-piperazin-1-yl)-benzamide as a light yellow solid, MS (EI): 267 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552088B2
Source datasetuspto-grants-2003_04
ORD IDord-8e176263995a49bfb7a69150c243181a
Source noteuspto-grants-2003_04