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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531430Generated: October 31, 2026

Ethyl Acetate → 5-Bromo-3-iodo-1H-pyrrolo(2,3-b)pyridine

https://huagongshe.com/reaction/531430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantN-IodosuccinimideHCID 120273—
Reactant5-bromo-1H-pyrrolo[2,3-b]pyridineHCID 10307932—
SolventAcetoneHCID 180—
SolventHexaneHCID 8058—
Product5-Bromo-3-iodo-1H-pyrrolo(2,3-b)pyridineHCID 2422921287.3%

Reaction Steps

5-Bromo-1H-pyrrolo[2,3-b]pyridine (5 g, 25 mmol) was dissolved in anhydrous acetone (75 ml) and added N-iodo succinimide (6.18 g, 27.5 mmol) under nitrogen atmosphere and stirred at RT for 2 h. The reaction was monitored by TLC (10% Ethyl acetate in hexane). The reaction mixture was cooled to RT and filtered, washed with cold acetone (50 ml) and dried under vacuum to afford 7.05 g (87% yield) of 5-bromo-3-iodo-1H-pyrrolo[2,3-b]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353107B2
Source datasetuspto-grants-2016_05
ORD IDord-088b0570349d489b98daa88c4df8e4c2
Source noteuspto-grants-2016_05