Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598383Generated: November 2, 2026

Triethylamine → HCID 68974210, compound

https://huagongshe.com/reaction/598383

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthoxyacetyl chlorideHCID 84189—
ReactantTert-butyl [4-(3-amino-7-benzyloxyquinolin-4-ylamino)butyl]carbamateHCID 68900070—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 68974210HCID 6897421092.5%

Reaction Steps

tert-Butyl {4-[3-amino-7-(benzyloxy)quinolin-4-ylamino]butyl}carbamate (28.1 g, 64.3 mmol) was dissolved in dichloromethane (319 mL). Ethoxyacetyl chloride (7.87 g, 64.5 mmol) was added dropwise via an addition funnel and the mixture was stirred for 1 hour. The dichloromethane was removed under reduced pressure and the resulting residue was dissolved in a solution of triethylamine (35.84 mL, 0.26 mol) and ethanol (319 mL). The reaction was heated at reflux for 4 hours, and then allowed to cool overnight. The solvent was evaporated under reduced pressure and the residue was dissolved in dichloromethane. The organic fraction was washed sequentially with water and saturated aqueous sodium chloride; dried over anhydrous sodium sulfate; filtered; and concentrated under reduced pressure. The oily residue was dissolved in acetonitrile. The acetonitrile was subsequently removed under reduced pressure to provide 30 g of tert-butyl [4-(7-benzyloxy-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]carbamate as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897597B2
Source datasetuspto-grants-2011_03
ORD IDord-b52891d9f8ec4169b30f7c7c64134580
Source noteuspto-grants-2011_03