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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734880Generated: October 29, 2026

Iodine → 2-(4-Chlorophenyl)-5-iodopyrazine

https://huagongshe.com/reaction/734880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantWaterHCID 962—
ReactantTert-Butyl nitriteHCID 10906—
Reactant5-(4-Chlorophenyl)pyrazin-2-amineHCID 20567029—
SolventCarbon TetrachlorideHCID 5943—
SolventDichloromethaneHCID 6344—
Product2-(4-Chlorophenyl)-5-iodopyrazineHCID 85969636—

Reaction Steps

In a flask protected from light, 4.90 mL (40.0 mmol) of tert-butylnitrite and 7.61 g (30.0 mmol) of iodine were added to a solution of 4.80 g (23.5 mmol) of 5-(4-chlorophenyl)pyrazin-2-ylamine in 100 mL of carbon tetrachloride and 50 mL of DCM. The mixture was stirred overnight at RT and then combined with 100 mL of water. The organic phase was washed twice with 50 mL of 10% aqueous sodium thiosulfate solution and 50 mL of water, dried over magnesium sulfate, filtered through activated charcoal, and evaporated down in vacuo. The residue was purified by column chromatography (silica gel, PE→PE/EtOAc 8:2). Yield: 3.40 g (46% of theoretical); C10H6ClIN2 (M=316.525); calc.: molpeak (M+H)+:317/319 (Cl); found: molpeak (M+H)+:317/319 (Cl); Rf value: 0.55 (silica gel, PE/EtOAc 9:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592358B2
Source datasetuspto-grants-2009_09
ORD IDord-a5fcf8228b004ee08e51b2a61654e541
Source noteuspto-grants-2009_09