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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 5-Fluoro-2-(piperazin-1-yl)pyrimidine | HCID 10058158 | — |
| Reactant | 5-Acetoxymethyl-2-phenyl-1H-imidazole | HCID 10176759 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 5-Fluoro-2-(4-((2-phenyl-1H-imidazol-5-yl)methyl)-1-piperazinyl)pyrimidine | HCID 9849910 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05905152 |
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| Source dataset | uspto-grants-1999_05 |
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| ORD ID | ord-4b1a142c08cc47d195f3dbf3af683da3 |
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| Source note | uspto-grants-1999_05 |
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