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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867552Generated: November 1, 2026

N,N'-Dimethylethylenediamine → HCID 67528572, compound

https://huagongshe.com/reaction/1867552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
Reactant1H-Pyrrolo(2,3-b)pyridineHCID 9222—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-(4-Iodophenyl)ethan-1-olHCID 3040770—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 67528572HCID 6752857288.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1.24 g (5 mmol) of 2-(4-iodophenyl)ethanol, 0.62 g (5.25 mmol) of 7-azaindole, 2.33 g (11.0 mmol) of potassium phosphate, 0.082 g (1.0 mmol) of N,N′-dimethylethylenediamine and 0.095 g (0.50 mmol) of cuprous iodide in 4 ml of toluene is heated at 80° C. overnight with thorough stirring under an argon atmosphere. The mixture is cooled to ambient temperature and diluted with 150 ml of ethyl acetate and 50 ml of water. After the phases have settled and been separated, the organic phase is washed with 25 ml of water and 25 ml of saturated aqueous sodium chloride solution. It is dried over sodium sulphate and evaporated to dryness. The residue is purified by chromatography on silica gel, eluting with a 70/30 then 60/40 and 50/50 mixture of cyclohexane and ethyl acetate, to give 1.05 g of product in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632850B2
Source datasetuspto-grants-2009_12
ORD IDord-8bf403d14b674a44b53be3519ba88f13
Source noteuspto-grants-2009_12