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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521328Generated: October 30, 2026

Ethanol → HCID 57447013, compound

https://huagongshe.com/reaction/521328

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 numberUS09328110B2
Source datasetuspto-grants-2016_05
ORD IDord-b0154bff08854d24aedd93df808e223b
Source noteuspto-grants-2016_05