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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363573Generated: October 29, 2026

Sodium Hydroxide → HCID 57515419, compound

https://huagongshe.com/reaction/1363573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthoxyacetyl chlorideHCID 84189—
ReactantHCID 57457820HCID 57457820—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 57515419HCID 5751541938%

Reaction Steps

Ethoxyacetyl chloride (9.00 g, 73.4 mmol) was reacted with tert-butyl 1-{[(3-aminoquinolin-4-yl)amino]methyl}cyclohexylcarbamate (27.2 g, 73.4 mmol) according to the method described in Part E of Example 9 and the resulting product was treated according to the method described in Part E of Example 9. After the solvent was removed to yield an oil, the oil was dissolved in ethanol (300 mL) and water (30 mL). Sodium hydroxide (4.3 g, 108 mmol) was added and the solution was heated at reflux for 6 h. The volatiles were removed under reduced pressure and the resulting brown oil was partitioned between dichloromethane (500 mL) and water. The organic layer was dried over Na2SO4, filtered, and concentrated under reduced pressure to yield a brown oil. Purification by flash chromatography (silica gel, 30% ethyl acetate/hexanes) provided tert-butyl 1-{[2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}cyclohexylcarbamate as a brown solid (11.9 g, 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884207B2
Source datasetuspto-grants-2011_02
ORD IDord-8ecbb00642ce49de8d1fc5153faffd3a
Source noteuspto-grants-2011_02