Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357631Generated: November 3, 2026

Piperazine → 2-[{4-(2-Pyridinyl)Benzyl}Oxy]-6-(1-Piperazinyl)Pyrazine

https://huagongshe.com/reaction/1357631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantPotassium CarbonateHCID 11430—
Reactant(4-(Pyridin-2-yl)phenyl)methanolHCID 1515239—
Reactant2-Chloro-6-[{4-(2-pyridinyl)benzyl}oxy]pyrazineHCID 18186935—
Product2-[{4-(2-Pyridinyl)Benzyl}Oxy]-6-(1-Piperazinyl)PyrazineHCID 18186937—

Reaction Steps

The title compound was prepared according to the procedure of example 50, step 2, starting from 2-chloro-6-[{4-(2-pyridinyl)benzyl}oxy]pyrazine (2.73 g, 9.16 mmol; obtained according to the procedure of example 50, step 1, starting from 4-(2-pyridinyl)benzyl alcohol*), piperazine (2.41 g, 27.9 mmol) and K2CO3 (1.33 g, 9.62 mmol) with the exception that the final filtration through alumina was omitted. The yield of the of the title compound was 2.06 g (65%) which was obtained as a beige colored oil that solidified when refrigerated. Purity 100% (HPLC). MS m/z 347 (M)+. HRMS m/z calcd for C20H21N5O (M)+ 347.1746, found 347.1749.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593330B2
Source datasetuspto-grants-2003_07
ORD IDord-9239b12adbff47d8bc3ff6729e32772f
Source noteuspto-grants-2003_07