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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387589Generated: October 25, 2026

Iodine → HCID 178490906, compound

https://huagongshe.com/reaction/387589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSodium BicarbonateHCID 516892—
ReactantPotassium bisulfateHCID 516920—
ReactantHCID 178490904HCID 178490904—
SolventEthanolHCID 702—
ProductHCID 178490906HCID 17849090694%

Reaction Conditions

Temperature0 °C

Reaction Steps

Diiodine (0.547 g, 2.16 mmol) in ethanol (5 mL) was added dropwise over 5 minutes to a solution of 1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-ol (0.50 g, 1.96 mmol, prepared similarly as that described in WO 2007/103308) in absolute ethanol (20 mL) at 0° C. The reaction was stirred at 0° C. for 3 hours, followed by addition of 5% sodium bicarbonate (20 mL). The mixture was concentrated to give a slurry. The pH was then adjusted with saturated KHSO4 to a pH of 4. The resulting solid was collected by filtration and dried to give 5-iodo-1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-ol (0.70 g, 94%). MS APCI (+) m/z 382.0 detected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372842B2
Source datasetuspto-grants-2013_02
ORD IDord-526f04bf4ae94df5a13eaf4fe84dee0b
Source noteuspto-grants-2013_02