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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075655Generated: October 26, 2026

Ethanol → 5-Fluoro-2-(4-((2-phenyl-1H-imidazol-5-yl)methyl)-1-piperazinyl)pyrimidine

https://huagongshe.com/reaction/1075655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTolueneHCID 1140—
Reactant5-Fluoro-2-(piperazin-1-yl)pyrimidineHCID 10058158—
Reactant5-Acetoxymethyl-2-phenyl-1H-imidazoleHCID 10176759—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventTriethylamineHCID 8471—
Product5-Fluoro-2-(4-((2-phenyl-1H-imidazol-5-yl)methyl)-1-piperazinyl)pyrimidineHCID 9849910—

Reaction Conditions

Temperature52.5 °C

Reaction Steps

Mix 5-fluoro-2-piperazinyl-pyrimidine (900 g), 5-acetoxymethyl-2-phenyl-1H-imidazole (1.17 Kg, 1.1 equivalents), DMAP (N,N-dimethylaminopyridine, 30 g), toluene (7.2 L), ethanol (1.8 L) and triethylamine (1.095 L) at 20-25° C., and heat the mixture with stirring at 50-55° C. until the reaction is complete (typically about 20-25 hours). Then add water (3.75 L) and cool the resulting suspension to 0-50° C. Filter off the product, wash it with water (6×1.4 L) and cold toluene (3×700 ml), and dry it under vacuum at 50-55° C. to constant weight.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05905152
Source datasetuspto-grants-1999_05
ORD IDord-4b1a142c08cc47d195f3dbf3af683da3
Source noteuspto-grants-1999_05