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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2089016Generated: October 30, 2026

N-bromobutanimide → 3-Bromo-5-methoxy-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/2089016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-methoxy-1H-pyrrolo[2,3-b]pyridineHCID 10307871—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo-5-methoxy-1H-pyrrolo[2,3-b]pyridineHCID 3781879955.8%

Reaction Steps

To a solution of 5-methoxy-1H-pyrrolo[2,3-b]pyridine (0.439 g, 2.96 mmol) in tetrahydrofuran (10 mL) was added N-bromosuccinimide (0.527 g, 2.96 mmol) at 0° C. After 90 minutes at 0° C., the reaction was quenched with 30% Na2S2O3 and extracted with EtOAc (2×). The combined organic layers were washed with water, dried and concentrated. The residue was triturated with EtOAc/diethyl ether (1:1) to give 0.375 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08435980B2
Source datasetuspto-grants-2013_05
ORD IDord-87c1426913244ae2a789d8a37f992e00
Source noteuspto-grants-2013_05