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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913100Generated: October 26, 2026

Potassium Iodide → 2-Iodo-8-(4-methoxyphenyl)-[1,2,4]triazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1913100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantSodium NitriteHCID 23668193—
Reactant8-(4-Methoxyphenyl)-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 59199005—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product2-Iodo-8-(4-methoxyphenyl)-[1,2,4]triazolo[1,5-a]pyridineHCID 5919909665.4%

Reaction Steps

A solution of potassium iodide (5.4 g, 32 mmol, 3.9 equiv) and sodium nitrite (1.73 g, 25.1 mmol, 3.00 equiv) in water (10 mL) was added over 5 min to a solution of 8-(4-methoxyphenyl)-[1,2,4]-triazolo[1,5-a]pyridin-2-amine (2.01 g, 8.36 mmol, 1 equiv) and p-toluenesulfonic acid (7.3 g, 38 mmol, 4.6 equiv) in acetonitrile at 24° C. After 19 h, the reaction mixture was diluted with ethyl acetate (250 mL), and the resulting solution was washed sequentially with water (2×120 mL) and saturated aqueous sodium chloride solution (120 mL). The collected organic was dried over magnesium sulfate, filtered, and concentrated in vacuo. Purification by flash column chromatography (20→30% ethyl acetate in heptane) provided product as a light yellow solid (1.92 g, 65% yield). 1H NMR (400 MHz, CDCl3), δ: 8.46 (dd, J=6.8, 1.0 Hz, 1 H), 7.96 (m, 2 H), 7.59 (dd, J=7.4, 1.1 Hz, 1 H), 7.01-7.06 (m, 3 H), 3.86 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609687B2
Source datasetuspto-grants-2013_12
ORD IDord-3369fa3545994e13bf1890be4a6feef4
Source noteuspto-grants-2013_12