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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1591579Generated: October 26, 2026

1-Methylpiperazine → HCID 178480770, compound

https://huagongshe.com/reaction/1591579

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant6-(4-chloro-2-pyridinyl)-2-pyridin-2-yl-1H-pyrimidin-4-oneHCID 178515630—
CatalystZincchlorideHCID 3007855—
Solvent2-Methyl-2-butanolHCID 6405—
ProductHCID 178480770HCID 178480770—

Reaction Steps

A mixture of 3.51 g (12.3 mmol) of 6-(4-chloropyrid-2-yl)-2-pyrid-2-yl-pyrimidin-4-ol, 27.4 ml (303 mmol, 20 equivalents, 30.38 g) of 1-methyl-piperazine and 84 mg (0.05 mmol, 0.05 equivalent) of zinc(II) chloride in 50 ml of 2-methyl-2-butanol is refluxed for 22 hours and concentrated to dryness using a rotary evaporator. 50 ml of water are added, 3.6 g of EDTA are added, and the pH is adjusted to 9 using dilute sodium hydroxide solution. Extraction is carried out three times using 150 ml of chloroform each time, and the organic extracts are combined and dried (sodium sulfate). Concentration is carried out using a rotary evaporator and the crude product is recrystallised from toluene. 6-[4-(4-Methyl-piperazin-1-yl)-pyrid-2-yl]-2-pyrid-2-yl-pyrimidin-4-ol is obtained in the form of a whitish solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291584B2
Source datasetuspto-grants-2007_11
ORD IDord-39eba654b162417ca0638b4a13f20a5a
Source noteuspto-grants-2007_11