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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2415034Generated: October 31, 2026

Imidazole → HCID 12151213, compound

https://huagongshe.com/reaction/2415034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantPropargyl alcoholHCID 7859—
ReactantSodium hydrideHCID 24758—
ReactantHCID 12151421HCID 12151421—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12151213HCID 1215121326.6%

Reaction Steps

4-Chloro-5-iodo-2-isopropylsulfonyl-6-trifluoromethypyrimidine (0.79 g) was dissolved in tetrahydrofuran (5.0 ml) and added propargyl alcohol (0.11 g). The mixture was cooled to ice bath temperature and added sodium hydride (oily 80%, 57 mg). The mixture was stirred at that temperature for 10 minutes, and then added imidazole (0.39 g) at the same temperature. The mixture was stirred at that temperature for 30 minutes, and then it warmed to room temperature. After stirring over night, the mixture was added water and extracted with ethyl acetate. The ethyl acetate layer was washed with water and brine, respectively and dried over magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography (chloroform-THF). The fraction was triturated by hexane to give 4-imidazol-1-yl-5-iodo-2-prop-2-ynyloxy-6-trifluoromethyl-pyrimidine (0.20 g) as colorless crystalline solid, mp 128-129° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06818631B1
Source datasetuspto-grants-2004_11
ORD IDord-0479e8c0601e4919bf9b44027f87dcb6
Source noteuspto-grants-2004_11