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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089042Generated: October 30, 2026

N-Iodosuccinimide → Methyl 3-iodo-1H-pyrrolo[2,3-b]pyridine-5-carboxylate

https://huagongshe.com/reaction/2089042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactantmethyl 1H-pyrrolo[2,3-b]pyridine-5-carboxylateHCID 22832049—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-iodo-1H-pyrrolo[2,3-b]pyridine-5-carboxylateHCID 24229255—

Reaction Steps

To a solution of Example 235a (1.04 g, 5.9 mmol) in 12 mL anhydrous DMF was added N-iodosuccinimide (1.46 g, 6.49 mmol) and the solution stirred at room temperature for 16 hours. The solvent was evaporated and the residue suspended in water and filtered. The collected solid was triturated with dichloromethane and the mixture filtered. The dichloromethane filtrate was concentrated to a brown powder that was carried on without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08435980B2
Source datasetuspto-grants-2013_05
ORD IDord-88e56c279d2b41248560f24fea579364
Source noteuspto-grants-2013_05