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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366652Generated: October 30, 2026

Ethanol → HCID 57447047, compound

https://huagongshe.com/reaction/2366652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTriethylamineHCID 8471—
ReactantEthoxyacetyl chlorideHCID 84189—
ReactantHCID 68874499HCID 68874499—
SolventDichloromethaneHCID 6344—
ProductHCID 57447047HCID 5744704798.8%

Reaction Steps

Ethyl N-(3-aminoquinolin-4-yl)-β-alaninate (20.0 g, 77.3 mmol, prepared in Parts A and B of Example 22) was treated with ethoxyacetyl chloride (11.29 g, 92.5 mmol) according to a modification the method described in Part A of Example 12. The reaction in dichloromethane (300 mL) was stirred for 1.5 hours, and after the addition of triethylamine (43.08 mL, 309.1 mmol) and ethanol (300 mL), the reaction was heated at reflux for four hours and then subjected to the work-up procedure to provide 25.0 g of ethyl 3-(2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)propanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697873B2
Source datasetuspto-grants-2014_04
ORD IDord-0585b1bb3c0e416d8911098d3cc5a057
Source noteuspto-grants-2014_04