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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401179Generated: November 3, 2026

Sodium Iodide → N-(3,5-dibromopyrazin-2-yl)-2-iodoacetamide

https://huagongshe.com/reaction/1401179

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant2-Chloro-N-(3,5-dibromopyrazin-2-yl)acetamideHCID 86696614—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
ProductN-(3,5-dibromopyrazin-2-yl)-2-iodoacetamideHCID 5829832578.3%

Reaction Steps

To a solution of 2-chloro-N-(3,5-dibromopyrazin-2-yl)acetamide (3.0 g, 9.11 mmol) in acetone (40 mL) was added sodium iodide (13.65 g, 91 mmol) dissolved in acetone (20 mL). Solution was allowed to stir at ambient temperature for 16 h. Solution was condensed under reduced pressure and diluted with ethyl acetate (500 mL) and washed consecutively with water (5×) to remove the blue color. Organics were dried over magnesium sulfate, filtered and solvent removed under reduced pressure to afford the crude product. The solid was diluted with 10% ethyl acetate in hexanes (40 mL) and sonicated while scraping the sides of the flask. The solution was then heated under a heat gun for 5 min, then cooled while sonicating at ambient temperature. The resulting solid was filtered and washed with additional hexanes and dried under vacuum to afford the title compound (3.0 g, 7.13 mmol, 78% yield). MS (ESI) m/z 420.3 [M−1]+, 422.0 [M+1]+, 424.0 [M+3]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907087B2
Source datasetuspto-grants-2014_12
ORD IDord-6586f4872ad74f7aa78515ad679b6e40
Source noteuspto-grants-2014_12