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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891000Generated: October 25, 2026

Ethyl Bromide → HCID 13006214, compound

https://huagongshe.com/reaction/891000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
Reactant1H-Pyrrolo(2,3-b)pyridineHCID 9222—
Reactant2,3-Dibromo-N-methylmaleimideHCID 18155—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13006214HCID 13006214—
ProductHCID 178418443HCID 178418443—

Reaction Steps

A solution of ethylmagnesium bromide is prepared, starting from magnesium (12.7 mmol) suspended in bromoethane (12.7 mmol) and dry tetrahydrofuran (5 ml). The solution is stirred at ambient temperature for 1 hour and then 7-azaindole (12.7 mmol), dissolved in 40 ml of anhydrous toluene, is added dropwise. After stirring at ambient temperature for 1 hour 30 minutes, a solution of N-methyl-2,3-dibromomaleimide (3.53 mmol) in 40 ml of anhydrous toluene is added dropwise. After 20 minutes, 60 ml of dry dichloromethane are added; the reaction mixture is then stirred at 40° C. for 75 hours and hydrolysed with saturated aqueous ammonium chloride solution. The organic product is extracted with ethyl acetate, and the organic phases are then combined, dried over magnesium sulphate and filtered. After evaporating off the solvent and purifying the residue by chromatography on silica gel (cyclohexane/ethyl acetate: 3/2), the expected product is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001906B2
Source datasetuspto-grants-2006_02
ORD IDord-f2c7b550815040e98b849e8a6a3f822c
Source noteuspto-grants-2006_02