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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856294Generated: October 29, 2026

Sodium Iodide → HCID 69635205, compound

https://huagongshe.com/reaction/856294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantOxiranemethanol, 4-methylbenzenesulfonate, (S)-HCID 153296—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178526855HCID 178526855—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 69635205HCID 6963520540%

Reaction Steps

A mixture of 2-chloro-4-nitro-1H-imidazole (6.1 g, 41.35 mmol), (S)-(+)-glycidyl tosylate (12.27 g, 53.75 mmol) and sodium hydrogencarbonate (7.3 g, 86.89 mmol) in ethanol (30 ml) was stirred under reflux for 9 hours. The reaction mixture was allowed to return to room temperature, then diluted with water, and the solution was extracted with methylene chloride twice. The extract was washed with a saturated saline solution, dried over magnesium sulfate and then filtered. The filtrate was concentrated to afford a foam. The resulting foam was dissolved in DMF (60 ml). To the solution, tert-butyl piperazine-1-carboxylate (8.47 g, 45.48 mmol), triethylamine (6.92 ml, 49.64 mmol) and sodium iodide (6.82 g, 45.5 mmol) were added followed by stirring at room temperature for 24 hours. The reaction mixture was poured into water, and extracted with ethyl acetate twice. The organic phases were combined, washed with water three times, dried over magnesium sulfate and then filtered. The filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate) to afford tert-butyl (R)-4-[3-(2-chloro-4-nitroimidazol-1-yl)-2-hydroxypropyl]piperazin-1-carboxylate (6.43 g, yield 40%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-dd53aa2e85e64506bf74fad1255bf6fc
Source noteuspto-grants-2007_08