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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241280Generated: October 26, 2026

Iodine → HCID 178428765, compound

https://huagongshe.com/reaction/2241280

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium HydroxideHCID 14797—
Reactant4-(5-chloro-2-methyl-4-nitrophenoxy)-1H-pyrazolo[3,4-b]pyridineHCID 68515911—
SolventDimethylformamideHCID 6228—
ProductHCID 178428765HCID 178428765—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 4-(5-chloro-2-methyl-4-nitrophenoxy)-1H-pyrazolo[3,4-b]pyridine (21.0 g, 68.9 mmol) in DMF (100 mL) was added freshly ground (mortar/pestle) potassium hydroxide (11.6 g, 207 mmol) flakes followed immediately by iodine (26.2 g, 103 mmol) under N2 at 25° C. The dark reaction was heated to 50° C. for 6 hours. The mixture was quenched by addition of aqueous 10% NaHSO3 (75 mL). The suspension was further diluted by addition of water (100 mL) and filtered. The resulting precipitate washed with water, dried by toluene azeotrope, and then left under high vacuum for 2 days. The beige powder (26.5 g, 69%) was carried forward without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723330B2
Source datasetuspto-grants-2010_05
ORD IDord-d5a98808af69453c8cda2ae1ee41163a
Source noteuspto-grants-2010_05