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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366544Generated: October 30, 2026

Methyl iodide → 1-(4-Benzylpiperazin-1-yl)-3-methyltetrahydropyrimidin-2(1H)-one

https://huagongshe.com/reaction/2366544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-(4-Benzylpiperazin-1-yl)tetrahydropyrimidin-2(1H)-oneHCID 67232518—
SolventTetrahydrofuranHCID 8028—
Product1-(4-Benzylpiperazin-1-yl)-3-methyltetrahydropyrimidin-2(1H)-oneHCID 68418829—

Reaction Steps

Lithium bis(trimethylsilyl)amide (1M THF solution; 1.5 mL) was added to a solution of 1-(4-benzylpiperazin-1-yl)tetrahydropyrimidin-2(1H)-one (0.27 g) obtained in Example 25a} in THF (10 mL) at 0° C., and the mixture was stirred at room temperature for one hour. Methyl iodide (0.09 mL) was added thereto, and the mixture was stirred at room temperature for 15 hours. The reaction mixture was concentrated under reduced pressure, and the residue was diluted with an aqueous sodium bicarbonate solution, and extracted with dichloromethane. The extract was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain the title compound (0.30 g, quantitative) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697865B2
Source datasetuspto-grants-2014_04
ORD IDord-a3dbf606eac24f83aa90a21acc8dfd67
Source noteuspto-grants-2014_04