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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181560Generated: November 1, 2026

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

https://huagongshe.com/reaction/2181560

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 numberUS06891044B2
Source datasetuspto-grants-2005_05
ORD IDord-dc81f3ee6cb24d128c3124d0de113908
Source noteuspto-grants-2005_05