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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362568Generated: November 1, 2026

Ethanol → HCID 57447013, compound

https://huagongshe.com/reaction/2362568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
ReactantEthoxyacetyl chlorideHCID 84189—
ReactantHCID 57447009HCID 57447009—
SolventDichloromethaneHCID 6344—
ProductHCID 57447013HCID 5744701398.7%

Reaction Steps

A solution of ethoxyacetyl chloride (7.00 g, 57.1 mmol) in dichloromethane (10 mL) was added dropwise to a stirred solution of ethyl 4-(3-aminoquinolin-4-ylamino)butyrate (prepared as described in Steps 1-2 of Example 17, 12.5 g, 45.7 mmol) in dichloromethane (100 mL) at room temperature. After 1.5 hours, the reaction mixture was concentrated under reduced pressure to afford a solid to which was added ethanol (100 mL) and triethylamine (17.4 mL, 125 mmol). The solution was left at room temperature for 5 days, then was heated at reflux for 2 hours. The solution was concentrated under reduced pressure. The residue was partitioned between dichloromethane (150 mL) and water (50 mL). The organic layer was washed with water (50 mL) and saturated aqueous sodium bicarbonate (50 mL), dried over potassium carbonate, filtered, and concentrated under reduced pressure to yield 15.4 g of ethyl 4-[2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]butanoate as a brown oil that was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691837B2
Source datasetuspto-grants-2014_04
ORD IDord-95ba999ca19c405e981c8c029566e4e6
Source noteuspto-grants-2014_04