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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862166Generated: October 30, 2026

Sodium Iodide → 1-(4-Iodo-pyrazolo[3,4-b]pyridin-1-yl)ethanone

https://huagongshe.com/reaction/1862166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantAcetyl chlorideHCID 6367—
Reactant4-Chloro-1H-pyrazolo[3,4-b]pyridineHCID 310045—
ReactantSodium BisulfiteHCID 23665763—
SolventAcetonitrileHCID 6342—
Product1-(4-Iodo-pyrazolo[3,4-b]pyridin-1-yl)ethanoneHCID 2187740042%

Reaction Steps

A mixture of 4-chloro-1H-pyrazolo[3,4-b]pyridine (820 mg, 5.30 mmol), sodium iodide (2.4 mg, 16.0 mmol), and acetyl chloride (0.8 ml) in acetonitrile (6 ml) was refluxed 8 h. The mixture was then treated with a 10% aqueous solution of NaCO3 (10 ml), and a 10% aqueous solution of NaHSO3 (10 ml), and held 10 min. The mixture was extracted with ethyl acetate (50 ml), and the organics were washed with brine (10 ml), dried over MgSO4, and evaporated under reduced pressure. Purification by silica gel chromatography gave 1-(4-iodo-pyrazolo[3,4-b]pyridin-1-yl)-ethanone as a brown solid (650 mg, 42%). 1H NMR (300 MHz, CDCl3) δ 8.39 (d, 1H, J=5.0 Hz), 8.04 (s, 1H), 7.76 (d, 1H, J=5.0 Hz), 2.88 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06534524B1
Source datasetuspto-grants-2003_03
ORD IDord-bba0bec224704a518f5db11a192a784a
Source noteuspto-grants-2003_03