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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431922Generated: October 26, 2026

1-Methylpiperazine → HCID 178480770, compound

https://huagongshe.com/reaction/1431922

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 numberUS07612010B2
Source datasetuspto-grants-2009_11
ORD IDord-88b0a74555e84873b24100e1678debb4
Source noteuspto-grants-2009_11