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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63595Generated: October 27, 2026

Potassium Hydroxide → 5-Bromo-3-iodo-1H-pyrrolo(2,3-b)pyridine

https://huagongshe.com/reaction/63595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantSodium ThiosulfateHCID 24477—
ReactantN-IodosuccinimideHCID 120273—
Reactant5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
SolventDichloromethaneHCID 6344—
Product5-Bromo-3-iodo-1H-pyrrolo(2,3-b)pyridineHCID 24229212—

Reaction Steps

To a solution of 5-bromo-1H-pyrrolo[2,3-b]-pyridine (commercial product, 1 g, 5.10 mmol) in 200 ml of CH2Cl2 is added KOH (145 mg, 2.55 mmol) at room temperature. After 30 minutes, N-iodosuccinimide (1.2 g, 5.10 mmol) is added and the solution is stirred for 15 hours, neutralized with saturated Na2S2O3 solution and extracted several times with CH2Cl2. The organic phases are combined, dried on MgSO4 and concentrated under reduced pressure. The expected product is obtained with a quantitative yield and used in the following step without additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447093B2
Source datasetuspto-grants-2016_09
ORD IDord-96d829c812d74501a86acdbdb74a4796
Source noteuspto-grants-2016_09