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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 495490Generated: October 29, 2026

Piperazine → HCID 22326795, compound

https://huagongshe.com/reaction/495490

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium CarbonateHCID 11430—
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 22326834HCID 22326834—
SolventAcetonitrileHCID 6342—
ProductHCID 22326795HCID 22326795—

Reaction Steps

A mixture of 1-(2-chloroethoxy)-2,3-dimethoxy-5-nitrobenzene (1.382 g, 5.28 mmol), K2CO3 (1.83 g, 13.2 mmol), and N-methylpiperazine (1.76 mL, 15.85 mmol) was stirred and heated under N2 in CH3CN (20 mL) under reflux overnight. The next day 0.80 g K2CO3 and 0.66 mL piperazine were added (1.1 eq.) and heated for 3 h more when HPLC showed that the reaction was complete. The solids were filtered and washed well with CH3CN and the filtrate was evaporated at 80° C. to remove excess amine. The resulting red oil was dissolved in CH2Cl2 and washed with water. The aqueous layer was washed with CH2Cl2. The combined organic layers were dried and evaporated giving 2,3-dimethoxy-1-(2-(4-methylpiperazin-1-yl)ethoxy)-5-nitrobenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06939874B2
Source datasetuspto-grants-2005_09
ORD IDord-6f6b830d5b124ba48cf853e7d664df0f
Source noteuspto-grants-2005_09