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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035477Generated: October 30, 2026

Iodine → HCID 66778502, compound

https://huagongshe.com/reaction/1035477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium HydroxideHCID 14797—
ReactantSodium SulfiteHCID 24437—
Reactant5-(1-Methyl-1H-pyrazol-4-YL)-1H-pyrrolo[2,3-B]pyridineHCID 58086111—
SolventDimethylformamideHCID 6228—
ProductHCID 66778502HCID 66778502—

Reaction Steps

8.2 A solution of 1.125 g (4.4 mmol) of iodine in 16 ml of DMF is slowly added dropwise at RT to a suspension of 901 mg (4.4 mmol) of 5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine and 620 mg (11.1 mmol) of KOH in 12 ml of DMF. When the addition is complete, the mixture is stirred at RT for a further 30 min. The reaction mixture is subsequently poured into 300 ml of an ice-cold, saturated sodium sulfite solution. The yellow precipitate is filtered off with suction and washed with 10 ml of ice-cold water. The filter residue is dried, giving 3-iodo-5-(1-methyl-1H-pyrazol-4-yl)-1H-pyrrolo[2,3-b]pyridine as beige crystals, ESI 325

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546390B2
Source datasetuspto-grants-2013_10
ORD IDord-a3d33ce300134f59bed061d5bad8e891
Source noteuspto-grants-2013_10