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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587430Generated: October 30, 2026

Potassium Iodide → HCID 58577728, compound

https://huagongshe.com/reaction/587430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantN,N'-DimethylethylenediamineHCID 8070—
Reactant1-Bromo-4-nitrobenzeneHCID 11466—
Reactant1,3-Dihydro-2H-pyrrolo(2,3-b)pyridin-2-oneHCID 13864095—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 58577728HCID 5857772825.2%

Reaction Conditions

Temperature95 °C

Reaction Steps

A mixture of 1H-pyrrolo[2,3-b]pyridin-2(3H)-one (431 mg), 1-bromo-4-nitrobenzene (778 mg), copper(I) iodide (122 mg), N1,N2-dimethylethane-1,2-diamine (113 mg) and potassium iodide (1.36 g) in 1,4-dioxane (10 mL) was sparged with argon for 5 min then heated overnight at 95° C. After this time, the reaction mixture was cooled to ambient temperature, diluted with ethyl acetate (100 mL), filtered through diatomaceous earth and the filtrate was concentrated under reduced pressure. The residue obtained was purified by chromatography (silica, heptane to 1:1 ethyl acetate/heptane) to afford 1-(4-nitrophenyl)-1,3-dihydro-2H-pyrrolo[2,3-b]pyridin-2-one (207 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226921B2
Source datasetuspto-grants-2016_01
ORD IDord-8dd84eeae2b84cfa9daae56bd60233b9
Source noteuspto-grants-2016_01