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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472055Generated: October 25, 2026

Ethylenediamine → [5-(2,6-diethyl-phenyl)-1-(4-isopropyl-phenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]-acetonitrile

https://huagongshe.com/reaction/472055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantCesium carbonateHCID 10796—
Reactantp-IodocumeneHCID 87073—
Reactant[5-(2,6-diethyl-phenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]-acetonitrileHCID 67152507—
CatalystCopper iodideHCID 83717—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product[5-(2,6-diethyl-phenyl)-1-(4-isopropyl-phenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]-acetonitrileHCID 67152418—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of [5-(2,6-diethyl-phenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]-acetonitrile (800 mg, 3.1 mmol), 1-iodo-4-isopropyl-benzene (1.13 g, 4.6 mmol), copper iodide (874 mg, 4.6 mmol), Cs2CO3 (1.50 g, 4.6 mmol) and ethylenediamine (30 μL, 4.6 mmol), and dioxane (100 mL) is heated to 60° C. under nitrogen for 18 h. The mixture is diluted with EtOAc and filtered over a small pad of silica gel. The obtained solution is concentrated under reduced pressure, and the residue is purified by chromatography on silica gel (hexane-EtOAc, 5:1) to afford [5-(2,6-diethyl-phenyl)-1-(4-isopropyl-phenyl)-1H-pyrrolo[2,3-c]pyridin-3-yl]-acetonitrile as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633193B2
Source datasetuspto-grants-2014_01
ORD IDord-e579c1238c0e42efae40a3f49c6e67a8
Source noteuspto-grants-2014_01