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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176925Generated: October 31, 2026

1-Methylpiperazine → HCID 67382819, compound

https://huagongshe.com/reaction/2176925

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 86623474HCID 86623474—
SolventWaterHCID 962—
ProductHCID 67382819HCID 6738281971%

Reaction Conditions

Temperature140 °C

Reaction Steps

A suspension of tert-butyl 2-(2-chloropyridin-4-yl)acetate (600 mg, 2.64 mmol) and N-methyl piperazine (2 ml) was heated in a sealed tube for 24 h at 140° C. The reaction mixture was cooled to room temperature, water was added and extracted with DCM. The combined organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated under vacuum to get the crude product. Purification by column chromatography over neutral alumina using 5% MeOH in CHCl3 as eluent afforded 600 mg (71%) of 1-(4-methylpiperazin-1-yl)-2-(2-(4-methylpiperazin-1-yl)pyridin-4-yl)ethanone as colorless liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067888B2
Source datasetuspto-grants-2015_06
ORD IDord-faa73ecd9e5a4849a3762341043ae6b9
Source noteuspto-grants-2015_06