Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359981Generated: November 3, 2026

Felbinac → HCID 86623034, compound

https://huagongshe.com/reaction/1359981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFelbinacHCID 3332—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantDioxane methylene chlorideHCID 18626912—
Reactantt-Butoxycarbonyl-aminopropanolHCID 23149331—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86623034HCID 8662303483%

Reaction Steps

Boc-aminopropanol (2.04 mmol), felbinac (2.04 mmol) (manufactured by Aldrich Chem. Co.) and DMAP (0.41 mmol) were dissolved in dioxane (7 ml) and then a dioxane-dichloromethane (3:4) solution (7 ml) of WSCI.HCl (2.35 mmol) was added thereto under ice-cooling. The reaction solution was clarified by adding dimethylformamide (DMF) (3 ml) and then returned to room temperature, followed by stirring overnight. Ethyl acetate was added thereto, followed by separation by washing with 5% aqueous citric acid solution, 5% aqueous sodium hydrogen carbonate solution and saturated brine consecutively. After dehydration drying with sodium sulfate, the solvent was evaporated under reduced pressure. The thus obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=3:1, 0.5% triethylamine) to give the titled compound (623.0 mg, yield 83%). The structure was identified by 1H-NMR (CDCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879817B2
Source datasetuspto-grants-2011_02
ORD IDord-489baa431aae40798fc8cbccdd4962c8
Source noteuspto-grants-2011_02